ACUSON Freestyle Diagnostic Ultrasound System User Manual: Siemens Medical Solutions USA, Inc

ACUSON Freestyle
Diagnostic Ultrasound System

User Manual
US
0123
Siemens Medical Solutions USA, Inc. 11002778_01 English

Product Version 3.5 CE Declaration
© 2014 Siemens Medical Solutions USA, Inc. This product is provided with a CE marking in
All Rights Reserved accordance with the regulations stated in Council
Directive 93/42/EEC of June 14, 1993 concerning
Medical Devices. The CE marking only applies to
August 2014
medical devices that have been put on the market
Printed in the United States of America
according to the above reference Council Directive.
Unauthorized changes to this product are not covered
ACUSON and ACUSON Freestyle are trademarks of by the CE marking and the related Declaration of
Siemens Medical Solutions USA, Inc. Conformity.
Asepti-Wipe, Cidex, Gigasept, MetriCide, T-Spray, EU Authorized Representative

Wavicide-01, Metrizyme, Sani-Cloth, Sterrad,
Siemens AG
Sterrad 100S, Sterrad SealSure, and Tyvek are
Medical Solutions
trademarks or registered trademarks of their
Henkestrasse 127
respective owners.
91052 Erlangen
Germany
Siemens reserves the right to change system
specifications at any time Siemens Global Headquarters
Siemens AG
Global Business Unit and Legal Manufacturer Wittelsbacherplatz 2
Siemens Medical Solutions USA, Inc. 80333 Muenchen
Ultrasound Germany
685 East Middlefield Road
Mountain View, CA 94043 Global Siemens Healthcare Headquarters
U.S.A. Siemens AG
Phone: +1-888-826-9702 Healthcare Sector
www.siemens.com/healthcare Henkestrasse 127
91052 Erlangen
Germany
Phone: +49 9131 84-0
www.siemens.com/healthcare

Contents
Chapter 1 Introduction
General overview of the ultrasound system.
Chapter 2 Safety and Care

Detailed information on system safety and how to care for and maintain the
system and transducers.
Chapter 3 System Setup

Detailed instructions on system setup and menus.
Chapter 4 Patient Studies

Detailed instructions on how to add and manage patient studies.
Chapter 5 Scanning
Detailed information on scanning modes and controls.
Chapter 6 Wireless Probe Operation

Detailed information about best operating procedures when using a wireless
probe.
Chapter 7 Batteries
Instructions for recharging and caring for probe and console batteries.
Chapter 8 Connectivity
Detailed information about configuring network and DICOM settings
ACUSON Freestyle User Manual iii

iv ACUSON Freestyle User Manual

About the User and Reference Manuals

The user and reference manuals consist of the following publications.
Publication Includes
User Manual ■■ Intended Audience
■■ Technical description of the ultrasound system
■■ Safety and care information for the system and compatible
transducers
■■ Descriptions of system controls
■■ Procedures for system setup and examination fundamentals
■■ Acoustic output data
System Reference ■■ Electromagnetic Compliance Information
■■ Wireless specifications, security, and quality of service
information
Customer Information ■■ Provides software release notes and updates to the User Manual
Note
ACUSON Freestyle User Manual v

Conventions
Read and understand these conventions used in this manual.
Warnings, Cautions, and

Notes
WARNING: Warnings are intended to alert you to the
importance of following the correct operating procedures where risk
of injury to the patient or system user exists.
CAUTION: Cautions are intended to alert you to the

importance of following correct operating procedures to prevent the
risk of damage to the system.
Note: Notes contain information concerning the proper use of the
system and/or correct execution of a procedure.
Probe and Transducer In accordance with ultrasound convention, these terms can be
interchangeable. For the ACUSON Freestyle, in this manual:
• Probe typically refers to the entire assembly of the handheld
scanning module which includes the probe transducer, electronics,
controls, and battery.
• Transducer typically refers to the scanning array at the tip of the
probe.
Key Text There are two types of Soft Keys on the system and they are
formatted differently in this manual:
• Bottom Soft Keys and their menu and sub-menu items: for
example, SETUP, VIEW, SETTINGS (formatting: bold, all caps).
• Real-time Control Bar Soft Keys and their menus and sub-menu
items: for example Freeze, Save Exam, Vascular (formatting:
bold, with gray bar).
vi ACUSON Freestyle User Manual

Intended Audience
The intended audience for the user and reference manuals includes the following users.
User Interaction with Ultrasound Equipment Expected Experience and Other Characteristics
Sonographer or ■■ Acquires diagnostic views of anatomy, ■■ Ranges from novices (for example
Nurse blood flow, and related pathology students) to advanced practitioners with
certification in multiple specialties
■■ Performs measurements and analysis of
the acquired images ■■ Educated in anatomy, physiology, patient
care, and identification of pathology in
■■ Performs ultrasound-guided procedures
ultrasound images
■■ Prepares exam data for review and
■■ Expert in ultrasound guided procedures
interpretation by a qualified physician
■■ Many sonographers and nurses have a
Bachelor’s degree in related health care
subjects
Physician ■■ Acquires diagnostic views of anatomy, ■■ Medical doctor
blood flow, and related pathology
■■ Expert in diagnostic imaging, including
■■ Performs measurements and analysis of computed tomography (CT), magnetic
the acquired images resonance imaging (MRI), X-ray,
ultrasound, and nuclear medicine
■■ Performs ultrasound-guided procedures
■■ Skilled in the interpretation of ultrasound
■■ Writes and assembles exam findings in a
exam data
report
■■ Expert in ultrasound-guided procedures
System ■■ Configures the ultrasound system for use ■■ A System Administrator is an individual
Administrator and in a networked environment within your organization who is designated
Customer Service to set up system parameters to connect
Engineer the ultrasound system or workstation to
a picture archiving and communication
system (PACS)
■■ Customer Service Engineers are
Siemens representatives who configure
the ultrasound system or workstation
during software installation and support
troubleshooting activities
ACUSON Freestyle User Manual vii

Freestyle Contents
About the User and Reference Manuals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . v
Conventions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . vi
Intended Audience . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . vii
1 Introduction
System Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3
System Console . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3
Console Front View. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3
Console Rear View . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-4
Console Inputs/Outputs Panel. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-5
Turning the System On and Off. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-6
Turn the System On. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-6
Turn the System Off. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-7
Imaging Screen Layout. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-8
Sample Imaging Screen. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-8
2 Safety and Care

Operating Safety and Environment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-3
Labels . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-3
System Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-3
Intended Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-6
Indications for Use. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-7
Fetal. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-7
Abdominal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-7
Intraoperative. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-7
Intraoperative Neurological . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-7
Pediatric. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-8
Small Organs. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-8
Neonatal Cephalic . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-8
Cardiac. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-8
Peripheral Vessel (Vascular). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-8
Musculoskeletal. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-8
Transducers and Intended Use. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-9
Biohazard Considerations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-10
Acoustic Output . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-11
ALARA / Prudent Use. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-11
Acoustic Output: Global Maximum Values. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-12
References: . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-12
Acoustic Terms and Definitions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-13
Accuracies. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-15
Measurement Accuracies . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-15
Accuracy by Transducer Type . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-15
Accuracy of Primary Measurements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-15
Distance. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-15
Area. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-15
Potential Sources of Measurement Error During Scanning. . . . . . . . . . . . . . . . . . . . . 2-16
viii ACUSON Freestyle User Manual

Electrical Safety. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-17

Level of Protection Against Electrical Shock for Probes . . . . . . . . . . . . . . . . . . . . . . . 2-19
Defibrillators . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-19
Implantable Devices . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-20
Possible Combinations with Other Equipment and Peripheral Equipment. . . . . . . . . 2-21
Important Information for Maintaining Data Integrity . . . . . . . . . . . . . . . . . . . . . . . . . . 2-24
Caring for the Ultrasound System. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-25
Daily Checklist. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-25
Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-26
Repair. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-26
Cleaning and Disinfecting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-27
Cleaning and Disinfecting Ultrasound System Surfaces . . . . . . . . . . . . . . . . . . . . . . . 2-27
Approved Disinfectant Wipes for the Ultrasound System Surfaces. . . . . . . . . . . . . . . 2-29
Caring for Documentation and Storage Devices. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-29
Caring for Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-30
Protective Case. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-30
Storage. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-30
Repair. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-30
Cleaning and Disinfecting Probes. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-31
Intraoperative Neurological Important Warnings. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-32
Probe General Cleaning (including Low Level Disinfection):. . . . . . . . . . . . . . . . . . . . . . 2-33
Probe High Level Disinfection. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-34
Preparation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-34
High-Level Disinfection. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-34
Probe Sterilization . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-34
Sterilization Preparation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-34
Probe Sterilization: Sterrad . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-35
IPX8 Immersion Levels . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-36
Approved List of Disinfectants. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-37
Caring for Probe Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-38
Probe Sheaths. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-38
Storage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-38
Recommended Use of the Probe Sheaths . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-39
Application. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-39
Disposal. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-39
Battery Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-40
Good Ergonomic Practices . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-42
Interrupt Scanning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-42
Positioning. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-42
Hand and Wrist. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-42
Exercise and Stretching. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-42
Moving the System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-43
ACUSON Freestyle Rollstand Configuration. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-44
System Upgrades . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-45
Performing System Software Upgrades. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-45
Environmental Protection. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-45
Product Recycling and Disposal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-45
Recycling Batteries . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-46
ACUSON Freestyle User Manual ix

Disposing of the Packaging Materials. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-46

Disposing of Components and Accessories. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-47
Energy Conservation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-47
Technical Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-48
3 Setup
System Setup and Controls. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3
Overview of the Setup Menu. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3
How to Select Items from the Setup Menu. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-4
Setup Menu Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5
Scan . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5
Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5
Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-6
System. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-7
Study List. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-9
New Patient Study. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-9
Close Study . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-9
4 Patient Studies
Protecting Patient Health Information. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-3
About Patient Studies. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-3
Patient Study Fields. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-4
Patient Soft Keys. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-5
Creating New Patient Studies. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-5
Using Patient Information from a DICOM Server. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-6
Worklist Query. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-6
Study Exam Types. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-6
Factory Exam Types. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-7
User-Defined Exam Types. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-8
The Study List. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-9
Viewing the List of Patient Studies. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-9
Sorting the Study List. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-9
Scrolling through the Study List. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-10
Selecting Multiple Studies for Export or Deletion. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-10
Viewing Images in a Study from the Study List . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-10
Managing Patient Studies. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-11
Exporting Patient Studies. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-11
How to Export Studies. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-11
Export Parameters. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-12
Editing Patient Studies. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-12
Deleting Patient Studies. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-12
5 Scanning
Using the Probe. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3
About the Probe. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3
Probe Orientation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3
Overview of the Probe. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3
Probe Controls. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-4
Locking and Unlocking the Probe. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-4
x ACUSON Freestyle User Manual

Probe Shortcuts for Save and Color. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-4

Connecting the Probe . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-5
Cabled Probe Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-5
Wireless Probe Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-6
The Real-Time Scanning Screen. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-7
Overview of the Scanning Process. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-8
Real-Time Scanning Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-9
Selecting an Exam Type from the List of Exams . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-11
Freezing an Image. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-11
Scanning Soft Keys . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-12
B-Mode Scanning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-13
B-Mode Tools. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-13
Color Flow Mode Scanning. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-15
Color Flow Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-15
Measurements. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-16
Performing a Measurement. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-16
Deleting Measurements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-16
Ellipse Measurement. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-16
Area Measurement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-17
Adding Text Annotations to Studies. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-18
Text Functions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-18
6 Wireless Probes
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-3
Antenna Locations. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-3
Equipment Setup for Optimal Scanning. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-4
Connecting a Wireless Probe. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-5
Problems Connecting. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-5
Wireless Signal Quality. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-6
Monitoring Wireless Signal Quality . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-7
Wireless Signal Quality Meter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-7
Average Noise Level Indicator. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-8
Wireless Noise Examples . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-10
B-Mode Wireless Noise. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-10
Color Flow Wireless Noise. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-10
Finding/Locating Wireless Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-11
Using Multiple Probes. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-12
More than One Wireless Probe . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-12
A Probe Connected via Adapter Cable. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-12
Powering Down the Probe . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-12
7 Batteries
Overview of the Probe Battery. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-3
Charging the Probe Battery. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-4
Checking the Status of Charging Batteries . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-4
Inserting the Battery into the Probe. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-5
Monitoring the Battery Charge Level while Scanning . . . . . . . . . . . . . . . . . . . . . . . . . . 7-5
Low Battery Alerts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-6
ACUSON Freestyle User Manual xi

8 Connectivity
Overview of Connectivity. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-3
Configuring the Network Settings. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-3
Ethernet Setup. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-3
Wireless Network Setup. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-4
Working with Multiple WiFi Networks. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-4
Detecting WiFi Networks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-4
Configuring the WiFi Network. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-5
Configuring the DICOM Setup. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-6
DICOM Setup Menu Soft Keys. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-6
Configuring a DICOM Storage Server. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-7
Configuring a DICOM Storage Commitment Server . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-8
Configuring a Modality Worklist Server . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-9
Configuring the System DICOM Settings. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-10
Freestyle Mobile Link App . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-11
Freestyle Mobile Link Settings. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-11
Privacy and Security . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-12
xii ACUSON Freestyle User Manual

Introduction
1 Introduction
A general overview of the ultrasound system and instructions on how to turn it on and off.
System Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3

System Console . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3
Console Front View. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3
Console Rear View . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-4
Console Inputs/Outputs Panel. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-5
Turning the System On and Off. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-6
Turn the System On. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-6
Turn the System Off. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-7
Imaging Screen Layout. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-8
Sample Imaging Screen. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-8
ACUSON Freestyle User Manual 1-1

Introduction
1-2 ACUSON Freestyle User Manual

Introduction
System Overview
The ACUSON Freestyle ultrasound system is designed for ultrasound studies. The system
offers a variety of scanning modes and probes. The system probes may be operated in
wireless mode, or using a probe Cable Adapter. The system provides an intuitive and easy-to-
operate user interface. It has a compact and portable design and offers DICOM archival and
networking capability.
System Console
Console Front View
PATIENT NAME
PATIENT ID XXX
L13-5
Nerve Gen XXX
2.5cm
G 9
CG 10
XXX
SC 3
SF 6 XXX
PP 10
55dB
XXX
CF 1
CP 1 7
Vel 1
Pri 4
XXX
20 Hz
XXX
XXX
ANL 0.0 dB
XXX XXX XXX XXX

P S
6
1
2
3 5
4
System Console: Front View
1. ON/OFF Button
2. SETUP Soft Key
3. Bottom Soft Keys
4. Trackball and Trackball Left and Right keys
5. Rotary knobs
6. Real-time Control bar Soft Keys
7. Real-time Control bar labels
8. Image Settings area

Introduction
Console Rear View
10
1 9
8
3
5 7
System Console: Rear View
1. Hand grip
2. I/O panel
3. VESA mount locations
4. Probe holders
5. Power Cable connector
6. Tilt stand
7. Service Use Only
8. System label
9. Service Use Only
10. Probe battery charge bays

Introduction
Console Inputs/Outputs Panel
Inputs/Outputs Panel along right side of system console
1. Probe Adapter Cable connector

2. For Service Only
3. Network connector
4. USB ports
5. 15-pin Video connector

Introduction
Turning the System On and Off

The Power key is located in the bottom, left corner of the system console control panel.
Location of Console Power Key
Turn the System On

To turn the system on, press the POWER key, holding it down momentarily. You will hear a beep
when power is started. The system will take a number of seconds to boot up.
NOTE: While the system is booting up, do not try to power down.

Introduction
Turn the System Off

To power the system down, press the POWER key, holding it down momentarily.
If you attempt to power the system down and the momentary pressing of the POWER key does
not shut the system off, hold the POWER key down continuously for five seconds to power
down. If you repeatedly have problems powering down, contact your service representative.
NOTE: If the system does not boot up when it is not plugged into the AC Mains
power outlet, it may be because the system battery is depleted. Plug the system into
AC mains power outlet using the power cable.
WARNING: Do not power down until an archival transfer is complete. If the system
is in the process of an archival transfer operation, such as saving a patient study to a
removable storage medium or over a network, powering down will terminate the transfer
and result in an unsuccessful transfer.
CAUTION: Do not power down during a software upgrade. Powering down during a
system software upgrade will cause the upgrade to terminate and be unsuccessful.

Introduction
Imaging Screen Layout

The console displays clinical images together with important operating parameters, patient
data, and control commands.
Sample Imaging Screen
8
7
PATIENT NAME
PATIENT ID XXX
L13-5
Nerve Gen XXX
2.5cm
G 9 XXX
6
CG 10
SC 3
SF 6 XXX
1
PP 10
55dB
CF 1 XXX
CP 1
Vel 1
Pri 4
XXX
20 Hz
XXX
XXX
5
ANL 0.0 dB
2
XXX XXX XXX XXX
P S 4
Sample ACUSON Freestyle Console Screen
1. Image area
2. Bottom Soft Keys
3. Wireless Signal Quality
4. Probe, System battery/power, Networking Status area
5. Frame Rate/Average Noise Level displays
6. Real-time Control Bar Soft Keys (e.g., Freeze, Save, Gain, etc.); controlled by touching
the bar and using the Rotary knob.
7. Image Settings area
8. Patient Name and ID

Safety and Care
2 Safety and Care

This chapter contains information regarding the safe operation of the ACUSON Freestyle
Ultrasound System, including a technical description of the system. Please read and
understand it prior to using the system in patient studies. Consult the System Reference
section of the Manual for important information about Electromagnetic Compatibility (EMC),
Wireless Security, and Wireless Quality of Service.
Operating Safety and Environment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-3

Labels . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-3
System Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-3
Intended Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-6
Indications for Use. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-7
Fetal. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-7
Abdominal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-7
Intraoperative. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-7
Intraoperative Neurological . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-7
Pediatric. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-8
Small Organs. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-8
Neonatal Cephalic . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-8
Cardiac. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-8
Peripheral Vessel (Vascular). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-8
Musculoskeletal. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-8
Transducers and Intended Use. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-9
Biohazard Considerations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-10
Acoustic Output . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-11
ALARA / Prudent Use. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-11
Acoustic Output: Global Maximum Values. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-12
References: . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-12
Acoustic Terms and Definitions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-13
Definition of Acoustic Terms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-14
Acoustic Output Global Maximum Values: B-Mode . . . . . . . . . . . . . . . . . . . . . . . 2-14
Acoustic Output Global Maximum Values: Color Doppler. . . . . . . . . . . . . . . . . . . 2-14
Accuracies. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-15
Measurement Accuracies . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-15
Accuracy by Transducer Type . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-15
Accuracy of Primary Measurements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-15
Distance. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-15
Area. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-15
Potential Sources of Measurement Error During Scanning. . . . . . . . . . . . . . . . . . . . . 2-16
Electrical Safety. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-17
Level of Protection Against Electrical Shock for Probes . . . . . . . . . . . . . . . . . . . . . . . 2-19
Defibrillators . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-19
Implantable Devices . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-20
Possible Combinations with Other Equipment and Peripheral Equipment. . . . . . . . . 2-21
Important Information for Maintaining Data Integrity . . . . . . . . . . . . . . . . . . . . . . . . . . 2-24
Caring for the Ultrasound System. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-25
Daily Checklist. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-25
Perform the following each day before using the ultrasound system:. . . . . . . . . . 2-25
Once the ultrasound system is powered on:. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-25
Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-26
Repair. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-26
Siemens Authorized Care. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-26

Safety and Care
Cleaning and Disinfecting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-27

Cleaning and Disinfecting Ultrasound System Surfaces . . . . . . . . . . . . . . . . . . . . . . . 2-27
Approved Disinfectant Wipes for the Ultrasound System Surfaces. . . . . . . . . . . . . . . 2-29
Caring for Documentation and Storage Devices. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-29
Caring for Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-30
Protective Case. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-30
Storage. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-30
Repair. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-30
Cleaning and Disinfecting Probes. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-31
Intraoperative Neurological Important Warnings. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-32
Probe General Cleaning (including Low Level Disinfection):. . . . . . . . . . . . . . . . . . . . . . 2-33
Probe High Level Disinfection. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-34
Preparation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-34
High-Level Disinfection. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-34
Probe Sterilization . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-34
Sterilization Preparation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-34
Probe Sterilization: Sterrad . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-35
IPX8 Immersion Levels . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-36
Approved List of Disinfectants. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-37
Caring for Probe Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-38
Probe Sheaths. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-38
Storage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-38
Recommended Use of the Probe Sheaths . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-39
Application. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-39
Disposal. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-39
Battery Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-40
Good Ergonomic Practices . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-42
Interrupt Scanning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-42
Positioning. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-42
Hand and Wrist. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-42
Exercise and Stretching. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-42
Moving the System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-43
ACUSON Freestyle Rollstand Configuration. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-44
System Upgrades . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-45
Performing System Software Upgrades. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-45
Environmental Protection. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-45
Product Recycling and Disposal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-45
Recycling Batteries . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-46
Disposing of the Packaging Materials. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-46
Disposing of Components and Accessories. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-47
Energy Conservation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-47
Technical Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-48

Safety and Care
Operating Safety and Environment

Do not operate the ultrasound system until you fully understand the safety considerations and
procedures presented in this manual.
WARNING: Failure to comply with Warnings may pose a threat to patient and/or user
safety.
Labels
For information regarding product labels, see the System Reference Manual.
System Symbols
Refer to this table to identify important symbols located on the ultrasound imaging system and
transducers.
NOTE: Some symbols in this table may not be used in your system.
Symbol Explanation
Caution: Risk of electric shock.
Consult instructions for use
Consult instructions for use
Caution
General Warning
(yellow and black illustration)
Standby — ON
USB Connection
Ethernet 10/100BaseT/1000BaseT Connection
Type B Applied Part

Safety and Care
Symbol Explanation
Do not dispose of by dumping in garbage. Use a separate collection for
electrical and electronic equipment.
Products bearing this symbol are subject to the European Community
directive 2002/96/EC on waste electrical and electronic equipment
(WEEE), amended by directive 2003/108/EC. For collection and disposal
of the product, its components, or its accessories, contact your local
Siemens representative.
Federal Communications Commission
Manufacturer's declaration of product compliance with applicable EEC

directive(s) and the European notified body
xxxx
Safety testing classified symbol for Canada and United States of America
IVK (Installierte Volumen Komponente)

Identifier of selected system components or parts for product traceability
60 C Probe storage temperature range
System storage temperature range
-20 C
Fuse. Identifies location of Fuse.

WARNING: Risk of Fire. Replace Fuse as marked.
Alternating Current (AC). Specifies the type of input voltage.
Transducer Connector port
Video Output. Connector for attaching video display monitor.
Electrostatic sensitive devices
Recyclable / Recoverable
Magnetic Field. WARNING: Keep battery-end of transducer at least 3

centimeters (1.3 inches) away from implanted cardiac rhythm devices.
Protective Earth Ground
IPX8 Protected against the effects of continuous immersion in water

Safety and Care
Symbol Explanation
Bar Code
Manufacturer
Year of Manufacture symbol with the year below
20xx
V~ AC (alternating current) voltage source
Indicates this side up
Do not allow to get wet
Fragile. Handle with care.
IEEE 802.11b/g (WiFi) connected
Battery (charge level)
Power Plug
I/O; for service use only.
Ethernet network
Study Storage Memory Used

Safety and Care
Intended Use
WARNING: The analysis of results from an ultrasound examination requires that you are
trained in the interpretation of diagnostic ultrasound studies and are qualified to make
clinical diagnoses.
Prescription Device Statement: In the United States of America, federal law restricts this device
to sale or use by, or on the order of, a physician.
The ACUSON Freestyle ultrasound system supports the applications listed in this
section.
WARNING: The ACUSON Freestyle ultrasound system is not intended for ophthalmic
studies.
WARNING: No claim is made regarding the safety or efficacy of ultrasound contrast

agents. It is important that you carefully follow the indications, instructions for use,
warning, and cautions that are provided by ultrasound contrast agent manufacturers as
part of the product labeling.
WARNING: Cardiac rhythm disturbances during perfusion studies using gas ultrasound
contrast agents have been observed in the diagnostic range of mechanical index (MI)
values. See the specific package insert for the contrast agent being used for details.
CAUTION: In performing fetal ultrasound studies, it is important to consult consensus

statements and health care organization guidelines for the use of ultrasound imaging in
pregnancy. Reference: Diagnostic Ultrasound Imaging in Pregnancy. NIH Consensus
Statement 1984 Feb 6-8;5(1):1-16
WARNING: Use sterile, endotoxin-free sheaths in intraoperative neurological scanning.

Disinfectant/sterilant residue left on the probe is neurotoxic and endotoxin is pyrogenic.
WARNING: Probe sheaths cannot be relied upon to prevent contamination of the probe
when used intraoperatively on patients with known or suspected Creutzfeld-Jakob disease
(CJD). A probe exposed to central nervous system tissue from know or suspected CJD or
Variant CJD should be destroyed since it may not be possible to sterilize. (See http://www.
cdc.gov/ncidod/qa_cid_infection_control.htm)

Safety and Care
Indications for Use

The indications for use (intended use) for the ACUSON Freestyle include fetal, abdominal,
intraoperative, intraoperative neurological, pediatric, small organs, neonatal cephalic, cardiac,
peripheral vessel and vascular, and musculoskeletal.
Scanning modes may include B-mode, Color Doppler, and Amplitude Doppler. Not all modes
may be activated on the system or available with all transducers or for all indicated uses.
Consult the Transducer Intended Use Table in this section. The system and probe may be used
in adult, pediatric, neonatal, and fetal patients.
Fetal
Fetal studies are performed to obtain images that can be used to: detect presence or absence
of structural abnormalities, image and measure anatomic and physiologic parameters of the
fetus, and determine blood flow patterns and velocities.
Abdominal
Abdominal studies are performed to obtain images that can be used to: detect presence or
absence of abdominal organ abnormalities, determine size, contour, and patency of vessels,
characterize obstructions, and determine blood flow patterns and velocities.
Intraoperative
Intraoperative studies are performed during surgical or interventional procedures to obtain
images that can be used to: identify organs and vessels, detect presence or absence of organ
abnormalities, determine size, contour, and patency of vessels, characterize obstructions,
determine blood flow patterns and velocities, and provide guidance and imaging of surgical
devices or instruments, such as needles, catheters, or biopsy instruments
Intraoperative Neurological
Intraoperative Neurological studies are performed during surgical procedures to obtain
images that can be used to: identify organs and vessels, detect presence or absence of organ
abnormalities, determine size, contour, and patency of vessels, characterize obstructions,
determine blood flow patterns and velocities, provide guidance and imaging of surgical devices
or instruments, such as needles, catheters, or biopsy instruments.

Safety and Care
Pediatric
Pediatric studies are performed in pediatric patients to obtain images that can be used to:
detect presence or absence of organ abnormalities, detect abnormalities in superficial and
bony structures, determine size, contour, and patency of vessels, and determine blood flow
patterns and velocities.
Small Organs
Small Organ studies are performed to obtain images of targets such as the breast, thyroid,
testicles, and lymph nodes that can be used to: detect presence or absence of organ
abnormalities, determine size, contour, and patency of vessels, and determine blood flow
patterns and velocities.
Neonatal Cephalic
Neonatal cephalic studies are performed in neonatal patients to obtain images that can be
used to: detect presence or absence of abnormalities, such as abnormal ventricle size or a shift
in the midline, or flow abnormalities.
Cardiac
Cardiac studies are performed to obtain images of the heart and associated vessels that can
be used to: detect presence or absence of abnormalities in heart anatomy, determine the blood
flow patterns and velocities, and image and measure anatomic and physiologic parameters of
the heart.
Peripheral Vessel (Vascular)

Peripheral vessel (vascular) studies are performed to obtain images that can be used to: detect
size, contour, and vessel patency, characterize obstructions, determine blood flow patterns and
velocities, and image and measure anatomic and physiologic parameters of vessels.
Musculoskeletal
Musculoskeletal studies are performed to obtain images of superficial and deeper targets such
as tendons, ligaments, muscles, and bony structures that can be used to: detect presence of
absence of anatomical abnormalities, and determine blood flow patterns and velocities.

Safety and Care
Transducers and Intended Use

NOTE: Certain probes may require features not available on your system.
Technical Data
Transducer Name Frequency Range
and Array Type Modes Intended Use Footprint
L8-3 Linear B-Mode Fetal, abdominal, 3.0 – 8.0 MHz
intraoperative,
Color Doppler intraoperative neurological, 38.4 x 5 mm
pediatric, small organs,
Amplitude Doppler neonatal cephalic,
cardiac, peripheral
vessel and vascular, and
musculoskeletal.
L13-5 Linear B-Mode Fetal, abdominal, 5.0 – 13.0 MHz
intraoperative,
Color Doppler intraoperative neurological, 25.6 x 4 mm
cardiac, peripheral
musculoskeletal.
C5-2 Curvilinear B-Mode Fetal, abdominal, 2.0 – 5.0 MHz
intraoperative,
Color Doppler intraoperative neurological, 13.0 x 60.00 mm
cardiac, peripheral
musculoskeletal.

Safety and Care
Biohazard Considerations
WARNING: Siemens makes every effort to manufacture safe and effective probes. You
must take all necessary precautions to eliminate the possibility of exposing patients,
operators, or third parties to hazardous or infectious materials. These precautions should
be considered in the use of any application that may indicate the need for such care, for
example, when scanning patients with open wounds.
WARNING: To eliminate the possibility of exposing patients, operators, or third parties

to hazardous or infectious materials, always dispose hazardous or infectious materials
according to local, state, and regional regulations.
WARNING: Probe Sheaths: There have been reports of severe allergic reactions to
medical devices containing latex (natural rubber). Health care professionals are advised
to identify latex sensitive patients and to be prepared to treat allergic reactions promptly.
For additional information in the U.S.A., refer to FDA Medical Alert MDA91-1.
WARNING: Ultrasound energy is transmitted more effectively through water than through
tissue. When using a standoff device of any kind, for example, a waterpath or gel pad, the
actual mechanical and thermal indices, MI and/or TI, may be higher than indicated in the
output display on the ultrasound system.
The assessment of the biological effects of diagnostic ultrasound on humans is a subject of

ongoing scientific research. This ultrasound system, and all diagnostic ultrasound procedures,
should be used for valid reasons, for the shortest possible period of time, and at the lowest
mechanical and thermal indices necessary to produce clinically acceptable images.
According to the principles of ALARA (As Low As Reasonably Achievable), the acoustic output
should be the lowest level required to satisfactorily perform the examination.
The ultrasound imaging system complies with the standards of the American Institute of
Ultrasound in Medicine (AIUM) and the National Electrical Manufacturers Association (NEMA),
the guidelines of the United States Food and Drug Administration (FDA) and the standards
of the International Electrotechnical Commission (IEC) in terms of safety and acoustic output
levels. The ultrasound output levels are stated to permit the user to critically evaluate the
ultrasound system settings in the event of new research findings being announced.

Safety and Care
Acoustic Output
WARNING: Ultrasound procedures should be used for valid reasons, for the shortest
period of time, and at the lowest mechanical/thermal index setting necessary to produce
clinically acceptable images.
NOTE: For ultrasound systems distributed in the United States of America, refer to
the Medical Ultrasound Safety ultrasound education program brochure produced by
the AIUM that is shipped with the system. This document explains the interaction of
ultrasound and tissue, the possibilities and mechanisms of bioeffects, and it explains
the terms used to describe acoustic output.
The ultrasound energy, frequency levels, and scanning times employed by the ACUSON
Freestyle have not been associated with harmful effects. Nevertheless, it is advisable to
minimize the patient’s exposure to ultrasound energy. This prudent use can be accomplished
by following the ALARA (As Low as Reasonably Achievable) Principle, and by operating the
system in a manner that reduces patient exposure to ultrasound energy. Acoustic Output
tables for the ACUSON Freestyle are provided below.
The acoustic output for the ACUSON Freestyle has been measured and calculated in
accordance with the “Acoustic Output Measurement Standard for Diagnostic Ultrasound
Equipment” (NEMA UD2-2004), and the “Standard for Real-Time Display of Thermal and
Mechanical Acoustic Output Indices on Diagnostic Ultrasound Equipment” (NEMA UD3-2004.)
ALARA / Prudent Use

Prudent use of ultrasound requires that patient exposure to ultrasound energy be limited to the
lowest output for the shortest period of time needed to obtain acceptable diagnostic results.
Techniques include:
1. Keep exams as brief as possible, consistent with diagnostic requirements.
2. Select the appropriate transducer for the patient body type and exam type in order to
optimize imaging results.
3. Use overall gain or dynamic range or post processing settings, which have no effect on
output, to optimize the image and obtain diagnostic results.
4. In general, as shown in the Acoustic Output Tables, Color Flow Doppler mode will have
higher output levels than B-Mode (2D). Keep this in mind when scanning. New studies
default to B-Mode.

Safety and Care
Acoustic Output: Global Maximum Values

No system/transducer combination is capable of exceeding either a Thermal Index (TI) of 1.0 or
a Mechanical Index (MI) of 1.0, so, in accordance with relevant standards (NEMA UD3-2004),
the system does not display MI or TI. The table below, Global Maximum Values, provides the
mean of the global maximum of acoustic output values. The terms are described below.
Table entries have been obtained with the same operating conditions that create the maximum
value.
Uncertainties associated with the values derive from transducer and system variability,
measurement variability, and engineering approximations for real-time calculations.
Measurement precision and uncertainty for quantities used to calculate the values in the table
are 30% for intensity and 15% for MI.
Maximum surface temperatures are in accordance with IEC 60601-2-37.
References:
Ziskin MC: “Measurement of uncertainty in ultrasonic exposimetry”, Ultrasonic Exposimetry,
M.C. Ziskin and P.A. Lewin, eds. (CRC Press, Boca Raton, FL) pp. 409-443, 1993.
Ziskin MC: “Specification of acoustic output level and measurement uncertainty in ultrasound
exposimetry,” IEEE Transactions Ultrasonics, Ferroelectrics, and Frequency Control, 50, 1023-
34, 2003

Safety and Care
Acoustic Terms and Definitions

Translations for language other than English.
Term Definition
Acoustic Output
Global Maximum Values
Term
Definition
ISPTA.3 (Intensity, spatial-
peal temporal average)
TI (Thermal Index)
TIC (Thermal Index Cranial)
TIS (Thermal Index Soft
Tissue)
TIB (Thermal Index Bone)
MI (Mechanical Index)
IPA.3@Mimax (Intensity,
pulse average at the
maximum MI)
B-Mode
Transducer Model
Type
Value
Color Doppler

Safety and Care
Definition of Acoustic Terms
Term Definition
ISPTA.3 Intensity, spatial-peak temporal average: The value of the temporal-
average intensity at the point in the acoustic field where the temporal-
average intensity is a maximum, or is a local maximum within a specified
region. Units: milliwatts/cm2.
TI Thermal Index: A quantity related to calculated or estimated temperature
rise under certain defined assumptions. The thermal index is the ratio
of total acoustic power to the acoustic power required to raise tissue
temperature by 1º C under defined assumptions. C: Cranial. S: Soft
tissue. B: Bone.
MI Mechanical Index: The spatial-peak value of the peak rarefactional
pressure, derated by 0.3 dB/cm-MHz at each point along the beam axis,
divided by the square root of the center frequency.
IPA.3@MImax Intensity, pulse average at the maximum MI: The ratio of the pulse
intensity integral to the pulse duration at the maximum MI. Units W/cm2.
Acoustic Output Global Maximum Values: B-Mode

TRACK 3 Summary (for systems with no probes having global maximum index values
exceeding 1.0)
Transducer
Model ISPTA.3 TI Type TI Value MI IPA.3@MImax
L8-3 3.58 mW/cm2 TIC 0.09 0.76 92.7 W/cm2
L13-5 1.15 mW/cm 2
TIS 0.02 0.33 31.74 W/cm2
C5-2 4.53 mW/cm2 TIC 0.15 0.76 67.21 W/cm2
Acoustic Output Global Maximum Values: Color Doppler

TRACK 3 Summary (for systems with no probes having global maximum index values
exceeding 1.0)
Transducer
Model ISPTA.3 TI Type TI Value MI IPA.3@MImax
L8-3 33.02 mW/cm 2
TIC 0.72 0.76 132.41 W/cm2
L13-5 54.49 mW/cm2 TIC 0.86 0.38 86.44 W/cm2
C5-2 19.09 mW/cm 2
TIC 0.88 0.76 75.18 W/cm2

Safety and Care
Accuracies
Measurement Accuracies
The ACUSON Freestyle may be used to provide measurements and calculations derived from
ultrasound images. The quantified image data may be used along with other clinical information
to assist a physician in making a patient diagnosis.
The sole reliance on diagnostic ultrasound data to make a clinical diagnosis is not
recommended. Numerous factors related to the accuracy of ultrasound image data must be
taken into account. This section describes some of these factors. Measurement accuracies are
also influenced by operator experience, scanning technique, interpreting physician experience,
and the technical difficulty of the patient. Many of these variables are not associated with the
ACUSON Freestyle system. This limits the ability to fully specify the clinical accuracy of the
measurements and calculations provided by the system.
Accuracy by Transducer Type

All transducer types have been verified for measurement accuracy in the modes appropriate to
each measurement type.
Because the moderate transducer frequency range of the system, measurement accuracies for
the system are not expected to vary significantly based on transducer used.
Accuracy of Primary Measurements

All reported accuracies are +/– one-half the least significant digit.
Distance
The system assumes that the speed of sound in tissue is 1540 meters per second and that
this speed is homogeneous in all tissues. The diagnostic ultrasound literature states that
differences in the speed of sound in the body do exist because of the differing tissue types. In
Clinical Sonography – A Practical Guide, (2nd Edition, Roger C. Sanders, ed., Little Brown and
Company 1991) the range is cited as from 1500 to 1600 meters per second. These differences
would produce an inaccuracy of up to +/– 4%.
The distance measurements on the system are verified using an AIUM standard phantom
with a fluid having an acoustic speed of approximately 1540 meters per second at room
temperature. The accuracy of this measurement is +/– 5%. The maximum range of this
measurement is 24 cm (dependent on the probe).
Area
The accuracy of the area measurement is +/– 10%.
The maximum range of this measurement is 733 cm2 (dependent on the probe).

Safety and Care
Potential Sources of Measurement Error During Scanning

The table below identifies potential sources of measurement error that may occur during
scanning. Awareness of these sources can help you avoid errors they may cause.
Potential Source
of Error Explanation of Error
Patient Variability The technical difficulty of patients in ultrasound imaging varies widely.
Greater care must be taken with technically difficult patients to obtain
the best images possible with the optimal transducer and system
control settings.
Operator Variability The skill, care, and experience of the person conducting the scan is
one of the most critical factors in obtaining accurate measurements.
Operator training should be consistent with the recommendations of the
appropriate professional medical societies.
Speed of Sound The image processing and measurement algorithms of diagnostic
ultrasound assume that the speed of sound in body tissue is 1540
meters per second. Different body tissues have different sound speeds.
In soft tissue there is approximately a 2% error; this may be as high as
5%, especially if fatty tissue is present in the area being measured.
Doppler Alignment When performing Doppler scans, try to align the Doppler sample as
close to parallel as possible.
Screen Pixel The display screen provided in the ACUSON Freestyle system is
Resolution comprised of a rectangular array of square picture elements (pixels).
WARNING Measurement pixel resolution is assumed to be +/– one pixel. The
maximum potential error of this resolution accuracy is 0.4%
Occasionally, a pixel or a group of pixels of the display may enter a fault
condition and become stuck in an on or off position. If stuck pixels occur
at a place where a measurement value is displayed, it could cause the
operator to misread the result. Pixels stuck in the on position may be
detected by looking at the screen with a dark background. Pixels stuck
in the off position will show up as dark against a bright video image. You
should periodically examine your system for stuck pixels and be aware
of this potential condition when reading measurements. If you believe
your system has stuck pixels, contact your Service Representative.

Safety and Care
Electrical Safety
WARNING: Explosion Hazard. Possible explosion hazard if used in the presence of
flammable anesthetics.
WARNING: To avoid electric shock, use a protective earth connection to connect the
ultrasound system to the AC Mains power supply. The protective earth connection
ensures that the mains circuit breaker will disconnect the power supply in the event of a
short circuit.
WARNING: To ensure grounding reliability, only connect the system to a hospital-grade

power outlet.
WARNING: The AC Mains power connector plug for the ultrasound system is a three
prong grounded plug (in the U.S.A.) and should never be adapted to any two prong (non
grounded) outlet, either by modifying the plug or by using an adapter. In the U.S.A.,
proper grounding requires the AC Mains power connector plug to be plugged into a
hospital grade power outlet.
WARNING: Risk of fire. Replace fuse as marked.
WARNING: To avoid electrical shock, never modify the ultrasound system AC Mains
power connector plug, as doing so may overload your facility’s power circuits. To ensure
grounding reliability, connect the system only to an equivalent outlet.
WARNING: To avoid electrical shock, never use equipment or an AC Mains power

cord that shows signs of wear or tampering, or that has a ground plug which has been
bypassed by using an adapter.
WARNING: Equipment connected to the ultrasound system and in the patient zone
must be powered from a medically isolated power source or must be a medically isolated
device. Equipment powered from a non isolated source can result in chassis leakage
currents exceeding safe levels. Chassis leakage current and patient leakage current
created by an accessory or device connected to a non isolated outlet may add to the
chassis leakage current of the ultrasound system.
WARNING: Using an extension cord or multi socket outlet setup to provide power to the
ultrasound system, or to the system’s peripheral devices may compromise the system
grounding and cause your system to exceed leakage current limits.
WARNING: To avoid electrical shock and damage to the ultrasound system, power
off and unplug the equipment from the AC Mains power outlet before cleaning and
disinfecting.
WARNING: To prevent excessive leakage current from contacting the patient, do not
touch a user-accessible connector on the system while touching or scanning the patient.
User-accessible connectors include connectors such as the USB connectors, and any
other audio, video, or data transmission connectors.

Safety and Care
WARNING: Connecting peripheral devices to accessory outlets on the ultrasound system

effectively creates a medical electrical system, resulting in a reduced level of safety.
WARNING: No modification of this equipment it allowed.
WARNING: Do not remove system covers. There are no operator serviceable parts
inside. Refer servicing to qualified personnel.
WARNING: To avoid the risk of electrical shock and fire hazard, inspect the system
probes and console on a regular basis for any damage to the enclosure, controls,
connectors or display, and do not use if damaged. Electrical safety tests must also be
performed at regular intervals as specified by local safety regulations, or as needed.
WARNING: To avoid the risk of electrical shock do not touch the probe battery recharging
contacts on the system console.
CAUTION: To avoid the possibility of static shock and damage to the ultrasound system,
avoid the use of aerosol spray cleaners on the monitor screens.
CAUTION: Do not use spray cleaners on the ultrasound system, as this may force
cleaning fluid into the system and damage electronic components. It is also possible for
the solvent fumes to build up and form flammable gases or damage internal components.
CAUTION: Do not pour any fluid onto the ultrasound system surfaces, as fluid seepage
into the electrical circuitry may cause excessive leakage current or system failure.
CAUTION: To ensure proper grounding and leakage current levels, it is the policy of
Siemens to have an authorized Siemens representative or Siemens approved third party
perform all on board connections of documentation and storage devices to the ultrasound
system.
CAUTION: To avoid the risk of electrical shock and fire hazard, inspect the system
probes and console on a regular basis for any damage to the enclosure, controls,
connectors or display, and do not use if damaged. Electrical safety tests must also be
performed at regular intervals as specified by local safety regulations, or as needed.
EMC Note: Proximity to sources of strong electromagnetic fields, such as radio
transmitter stations or similar installations may lead to interference visible on the monitor
screen. However, the device has been designed and tested to withstand such interference
and will not be permanently damaged.
CAUTION: Total system chassis risk current should not exceed 100 microamps.
CAUTION: Do not position the system to make it difficult to disconnect the power cable
connector/plug.
CAUTION: If the probe overtemp or probe battery overtemp message appears, the
system will stop imaging and the image will be frozen. Unfreeze will not function until the
overtemp condition terminates.

Safety and Care
Level of Protection Against Electrical Shock for Probes

According to EN 60601-1 and IEC 60601-1, the assemblies for the probes provide a “Level of
Protection Against Electrical Shock” of “Type B.”
The Type B icon is located on the probe and probe connector labels
Defibrillators
WARNING: To avoid the risk of injury to the operator, remove the probe from patient
contact before the application of a high-voltage defibrillation pulse.
For patient safety, be sure to use defibrillators that do not have grounded patient circuits.

Safety and Care
Implantable Devices
WARNING: Ultrasound systems, like other medical equipment, use high-frequency
electrical signals that can interfere with implantable devices such as pacemakers and
implantable cardioverter-defibrillators (ICDs). If the patient has such an implantable
device, you should be aware of any interference in its operation and immediately power
off the ultrasound system.
WARNING: The probe battery and probe adapter cable well at the back of the probe,
away from the transducer end (see illustration) into which the probe battery or cable
adapter are placed, contains magnets used to secure the probe battery and cable
adapter. Keep this end of the probe at least 3 cm (1.3 inches) away from implanted
cardiac rhythm devices.
Probe battery (showing connector side); insert with battery connectors facing down
1. Probe battery/cable adapter well

2. Location of magnets

Safety and Care
Possible Combinations with Other Equipment and Peripheral

Equipment
WARNING: Accessory equipment connected to the analog and digital interfaces must be
certified according to the respective EN and IEC standards (for example, EN 60950 and
IEC 60950 for data processing equipment and EN 60601-1 and IEC 60601-1 for medical
equipment). Furthermore, all configurations shall comply with the system standards EN
60601-1-1 and IEC 60601-1-1. Anyone who connects additional equipment to the signal
input or signal output port configures a medical system and is therefore responsible that
the system complies with the requirements of the system standards EN 60601-1-1 and
IEC 60601-1-1. Siemens can only guarantee the performance and safety of the devices
recommended by Siemens. If in doubt, consult the Siemens service department or your
local Siemens representative.
WARNING: Do not use an accessory or peripheral device, such as an external monitor

within 1.5 meters (1.83 meters [6 feet] in Canada and the U.S.A.) of a patient (beyond the
perimeter of the bed — examination table, treatment surface, and the like) and extending
vertically 2.29 meters (7.5 feet) above the floor, unless the device receives power from an
isolation transformer that meets medical safety standards.
The ultrasound system supports a maximum of two documentation or storage devices

connected to the system. Siemens recommends that you power off each device whenever the
system is powered off.
CAUTION: Any on-board peripheral devices must be installed by an authorized Siemens

representative or by a Siemens-approved third party. Devices installed by other people
will be at the user’s risk and may void the system warranty.
In order to fulfill EN 60601-1-1 and IEC 60601-1-1 (Medical Electrical Equipment, Part 1:
General Requirements for Safety) requirements, connection of peripheral equipment to your
ultrasound system much adhere to one of the following conditions:
■■ The peripheral equipment itself is a medical device approved according to EN 60601-1
and IEC 60601-1, or
■■ Non-medical peripheral equipment approved according to any other EN or IEC standard
(EN XXXXX or IEC XXXXX, e.g., equipment complying with EN 60348 and IEC 60348, EN
60950 and IEC 60950, etc.) must use the following setup for connection:
–– The peripheral equipment is located at least 1.5 meters (1.83 meters [6 feet] in Canada and
the U.S.A.) outside the patient environment and extending vertically 2.29 meters (7.5 feet)
above the floor. A patient environment is defined as the area in which medical examination,
monitoring, or treatment of the patient takes place (examination table, treatment surface, and
the like).
–– The peripheral equipment is connected to a main outlet outside the patient environment but
still within the same room as the ultrasound system
–– The peripheral equipment is connected to the ultrasound system using isolation adapters.

Safety and Care
4 3
Example of a peripheral equipment connection and patient environment
1. Patient environment represented by shading, extending exactly 1.5 meters (1.83 meters
[6 feet] in Canada and in the U.S.A.) around patient and ultrasound system
2. Ultrasound system power cord
3. Medically-approved isolation transformer power cord
4. Medically-approved isolation transformer
5. Peripheral equipment power cord
6. Peripheral equipment (EN XXXXX and IEC XXXXX)
7. Peripheral equipment connections cable
8. Ultrasound system

Safety and Care
Example of a peripheral equipment connection and patient environment
1. 2.29 meters
2. 1.5 meters (1.83 meters [6 feet] in Canada and the U.S.A.)

Safety and Care
Important Information for Maintaining Data Integrity

CAUTION: To prevent corruption of data stored on inserted media, do not interrupt the
exporting process. Do not delete exported patient data from the local database until the
exporting process is complete and the inserted media is determined to be full (or no more
exporting is planned for the inserted media).
■■ To prevent the loss of data that results from power failures and other system “down”
occurrences, you must archive important data, such as patient records, onto a network or
an external recording medium, such as a USB, or DICOM storage device.
■■ Loss of data is to be expected and its retrieval is not normally possible under the following
conditions: loss of power to the ultrasound system, hard disk failure, CPU failure, system
lockup, and other similar causes.
■■ Should an abnormal system shutdown occur, retrieval of data not saved to the hard disk or
not archived to an external recording media is not normally possible.
■■ An abnormal system shutdown occurs if you do not power off the ultrasound system using
the power on/off key located on the control panel. Other examples of abnormal system
shutdown include:
–– Equipment malfunction
–– Loss of power
–– Accidental removal of the power cord
–– Pressing and holding the power on/off switch longer than four seconds
■■ Should an abnormal system shutdown occur, the system may initially require additional
time to reboot or to respond to user input.

Safety and Care
Caring for the Ultrasound System

It is the responsibility of the user to verify that the ultrasound system is safe for diagnostic
operation on a daily basis. Each day, prior to using the system, perform each of the steps in the
Daily Checklist.
All exterior parts of the ultrasound system, including the control panel, keyboard, system
accessories, probes, and probe accessories, should be cleaned and/or disinfected as
necessary or between uses. Clean each component to remove any surface particles. Disinfect
components to kill vegetative organisms and viruses.
Daily Checklist
WARNING: To minimize the risk of cross contamination and infectious diseases, a sterile,
non pyrogenic probe sheath must be in place during procedures requiring sterility.
WARNING: To avoid electrical shock, you must visually inspect a probe prior to use. Do
not use a probe that has a cracked, punctured, or discolored casing or a frayed probe
adapter cable.
Discoloration Exception: The use of the approved disinfectants, Cidex OPA and Gigasept FF,
may cause discoloration of probe housings, including the face of the probe. You can continue
to use a probe if it is discolored due to the use of these specific disinfectants only.
Perform the following each day before using the ultrasound system:
■■ Visually inspect all probes. Do not use a probe that has a cracked, punctured, or
discolored casing or a frayed probe adapter cable.
■■ Visually inspect all power cords. Do not power on the ultrasound system if a cord is frayed
or split, or shows signs of wear.
■■ Verify that the Trackball, Rotary knobs, Soft Keys, and other controls on the control panel
appear clean and free from gel or other contaminants.
Once the ultrasound system is powered on:
■■ Visually check the on screen displays and lighting.
■■ Verify that the monitor displays the current date and time.
■■ Verify that the probe identification and indicated frequency are correct for the active probe.

Safety and Care
Maintenance
CAUTION: Electrical safety tests must also be performed at regular intervals as specified
by local safety regulations, or as needed.
Repair
WARNING: No modification of this equipment is allowed.
For questions regarding repair or replacement of any equipment parts on your system, contact
your Siemens service representative.
Siemens Authorized Care
Installers and operators must observe any statutory regulations that govern the installation,
operation, inspection, and maintenance of this equipment.
Perform inspections and maintenance at the prescribed intervals to avoid worn and hazardous
parts due to wear.
As manufacturers and installers of ultrasound equipment, Siemens cannot assume
responsibility for the safety properties, reliability, and/or performance of the equipment, if:
■■ Installations, extensions, readjustments, modifications, additions, or repairs are carried out
by persons not specifically authorized by Siemens.
■■ Components that affect the safe operation of the system are replaced by parts not
authorized by Siemens.
■■ The electrical installation of the room where the equipment is located does not meet the
power and environmental requirements stated in this manual.
■■ The equipment is not used in accordance with the operating instructions.
■■ The system is operated by personnel not adequately educated or trained.
Siemens suggests that you request any person who performs maintenance or repairs to
provide you with a certificate showing:
■■ The nature and extent of the work performed
■■ Changes in rated performance
■■ Changes in working ranges
■■ Date of service
■■ Name of person or firm performing the service
■■ Signature of person performing the service
Technical documentation pertinent to the ultrasound system is available at an additional
charge. However, this does not in any way constitute an authorization to conduct repairs or
maintenance. Siemens refuses all responsibility whatsoever for repairs that are performed
without the express written consent of the Siemens service department.

Safety and Care
Cleaning and Disinfecting

You must take all necessary precautions to eliminate the possibility of exposing patients,
operators, or third parties to hazardous or infectious materials. Use universal precautions when
cleaning and disinfecting. You should treat all portions of the ultrasound system that come in
contact with human blood or other body fluids as if they were known to be infectious.
All exterior parts of the ultrasound system, including the control panel, system accessories,
probes, and probe accessories, should be cleaned and/or disinfected as necessary or between
uses. Clean each component to remove any surface particles. Disinfect components to kill
vegetative organisms and viruses.
Cleaning and Disinfecting Ultrasound System Surfaces
WARNING: To avoid electrical shock and damage to the ultrasound system, power off
and unplug the equipment from the AC power outlet before cleaning and disinfecting.
WARNING: Disinfectants and cleaning methods listed are recommended by Siemens for
compatibility with product materials, not for biological effectiveness. Refer to disinfectant
label instructions for guidance on disinfection efficacy and appropriate clinical uses.
WARNING: Do not immerse any part of the system console in Liquid.
WARNING: Always wear protective clothing, including eye wear and gloves, when
performing cleaning and disinfection.
WARNING: The use of any disinfectants other than those specified in the instructions for
use may damage the ultrasound system and accessory surfaces and, as a result, may
create electrical hazards for the patients and/or users.
CAUTION: To avoid the possibility of static shock and damage to the ultrasound system,
avoid the use of aerosol spray cleaners on the monitor screen.
CAUTION: Do not clean the ultrasound system with chlorinated or aromatic solvents,
acidic or basic solutions, isopropyl alcohol or strong cleaners such as ammoniated
products, as these can damage the surface of the system. Use of unapproved cleaners or
disinfectants can result in severe damage to the ultrasound system components. Use the
recommended cleaning procedure.
CAUTION: Do not use spray cleaners on the ultrasound system, as this may force
cleaning fluid into the system and damage electronic components. It is also possible for
the solvent fumes to build up and form flammable gases or damage internal components.
CAUTION: Do not pour any fluid onto the ultrasound system surfaces, as fluid seepage
into the electrical circuitry may cause excessive leakage current or system failure.
CAUTION: Do not use abrasive cloths or brushes when cleaning any part of the system.
Use only soft cloths, gauze pads, or brushes. Apply solutions to the cloth, not the system.
CAUTION: To clean the lens cover of the system display monitor, use only a soft cloth
lightly moistened with a mild lens or glass cleaner. Using other cleaners may damage the
display and void the warranty.

Safety and Care
The following instructions describe cleaning the surface of the ultrasound system, including the
Trackball and probe holder. See also, “Approved Disinfectant Wipes for the Ultrasound System
Surfaces” on page 2-29.
To Do This
Clean and disinfect 1. Power off the ultrasound system and unplug the power cord from the power
the surface of the outlet.
ultrasound system 2. Use a clean gauze pad or lint-free cloth, lightly moistened with a mild detergent,
to wipe the surface of the ultrasound system.
Take particular care to clean the areas near the Trackball, Soft Keys, and Rotary
knobs. Ensure these areas are free of coupling agent (gel) and any other visible
residue.
Ensure that cleaning solution does not seep into the control panel, or any other
openings.
3. After cleaning, use a clean, lint-free cloth to dry the surface.
4. As required, use an approved disinfectant wipe to disinfect the ultrasound system
and accessories.
5. Reconnect the ultrasound system power cord into the power outlet.
Clean and disinfect the 1. Remove the holder from the ultrasound system.
holders for probes a. Squeeze the tab at the top of the probe holder away from the system console
and pull the holder upward.
2. Clean the holder under running water, using a mild detergent, and dry with a lint
free cloth.
3. As required, use an approved disinfectant wipe to disinfect the holder.
4. Reattach the holder to the ultrasound system pressing downward until the tab
clicks into place.
Clean and disinfect the CAUTION: Do not drop or place foreign objects inside the
Trackball Trackball assembly because doing so may affect the Trackball
operation and damage the ultrasound system.
1. Rotate the Trackball bezel counterclockwise and lift up to remove the Trackball
bezel from the control panel.
2. Carefully remove the Trackball from the control panel.
3. Clean the bezel and Trackball with a cotton swab or lint free pad moistened with
mild detergent solution.
4. Clean the inside of the Trackball assembly using a cotton swab moistened with
mild detergent solution.
5. As required, use an approved disinfectant wipe to disinfect the Trackball,
Trackball bezel, and Trackball assembly.
6. Allow the Trackball components to completely dry before reassembly.
7. Reinstall the Trackball and replace the Trackball bezel.
a. Place the Trackball inside the Trackball assembly.
b. Place the Trackball bezel over the Trackball.
c. Rotate the Trackball bezel to tighten. Do not overtighten the Trackball bezel.

Safety and Care
Approved Disinfectant Wipes for the Ultrasound System Surfaces

The following matrix provides a list of approved disinfectant wipes for use on the ultrasound
system and surfaces of the listed accessories.
Sani-Cloth Sani-Cloth Sani-Cloth Super Sani-

Sani-Cloth Bleach Wipe* HB Plus Cloth
Ultrasound System     
Probe Holders     
Trackball Assembly     
*or any bleach wipe with <1% sodium hypochlorite and no other active ingredients
 = Compatible
Caring for Documentation and Storage Devices

For information on the care of an optional documentation or storage device, refer to the
manufacturer’s operating instructions that accompanied the device.

Safety and Care
Caring for Probes

WARNING: During neurosurgical procedures, if a probe becomes contaminated with
tissue or fluids of a patient known to have Creutzfeldt Jakob disease, the probe should be
destroyed as it cannot be sterilized.
CAUTION: Probes are sensitive instruments — irreparable damage may occur if they
are dropped, knocked against other objects, cut, or punctured. Do not attempt to repair or
alter any part of a probe, contact your local Siemens representative.
CAUTION: To avoid cable damage, do not roll the ultrasound system over probe adapter
cables.
CAUTION: To avoid damage to the probe, do not use probe sheaths containing an oil
based coating or petroleum or mineral oil based ultrasound coupling agents. Use only a
water based ultrasound coupling agent.
CAUTION: Follow all instructions provided by manufacturers of sterile goods (probe

sheaths) to ensure proper handling, storage, and cycling of all sterile goods.
CAUTION: Take extreme care when handling or storing probes. They must not be
dropped, jarred, or knocked against other objects. Do not allow probes to come into
contact with any sharp edged or pointed object.
Protective Case
Due to the mechanical sensitivity of probes, Siemens recommends that you always use the
probe case when you ship a probe or transport it from one place of examination to another. The
case is specially designed to protect the sensitive parts of the probe. Be sure that all parts of
the probe are properly placed inside the case before you close the lid.
Storage
Store probes in a clean and dry environment. Extreme temperatures or humidity may damage
a probe.
Repair
Do not attempt to repair or alter any part of the probe. Contact your service representative at
Siemens immediately if a probe appears to be damaged or malfunctions in any way.

Safety and Care
Cleaning and Disinfecting Probes
WARNING: Before cleaning and disinfecting, you must read and understand the cleaning
and disinfecting topic, including the warnings and cautions for cleaning and disinfecting
ultrasound system surfaces provided in this chapter.
WARNING: Follow the instructions in this chapter, and your institution’s procedures to
avoid risk of infection.
WARNING: Probes used in semi-critical applications should be sterilized between uses

whenever feasible though high level disinfection is minimally acceptable. In addition, the
use of a sheath is recommended for every semi-critical use. Probes used in a semi-critical
application should be cleaned and sterilized or at least receive high level disinfection after
use, even if a sheath was used.
WARNING: Probes used in critical applications should be sterilized and the use of a
sterile sheath is recommended. Probes used in critical applications should be cleaned and
sterilized after use even if a sterile sheath was used.
NOTE: When sterilization is not possible, an accepted method of infection control for
critical use is high-level disinfection and the use of a sterile gel and a sterile probe
cover. (See US FDA Guidance document, “Information for Manufacturers Seeking
Marketing Clearance of Diagnostic Ultrasound Systems and Transducers” dated
September 9, 2008 at www.fda.gov/downloads.) Use only sterile, legally marketed
probe sheaths for semi-critical or critical applications.
WARNING: ACUSON Freestyle probes may only be sterilized using the Sterrad method,
(Sterrad model 100S). Do not attempt to sterilize a transducer using steam, autoclaving,
ultraviolet, gamma radiation, dry heat, ethylene oxide, or other methods.
WARNING: Unless explicitly stated otherwise, ACUSON Freestyle transducers are not
indicated or intended for endo-scanning uses.
WARNING: Always wear protective clothing, including eye wear and gloves, when
performing cleaning and disinfection.
WARNING: Clean the probe modules by hand. Do not use an ultrasonic cleaner or
automatic washer.
WARNING: Inspect transducers for signs of wear or damage prior to use and prior to
cleaning, disinfection, or sterilization. Do not process a probe that exhibits signs of wear
or damage, such as cracks or fractures in the enclosure.

Safety and Care
Intraoperative Neurological Important Warnings
WARNING: Use sterile, endotoxin-free sheaths in intraoperative neurological scanning.

Disinfectant/sterilant residue left on the probe is neurotoxic and endotoxin is pyrogenic.
WARNING: Probe sheaths cannot be relied upon to prevent contamination of the probe
when used intraoperatively on patients with known or suspected Creutzfeld-Jakob disease
(CJD). A probe exposed to central nervous system tissue from know or suspected CJD or
Variant CJD should be destroyed since it may not be possible to sterilize. (See http://www.
cdc.gov/ncidod/qa_cid_infection_control.htm)
WARNING: To avoid electrical shock and damage to the system, power down and
disconnect the probe prior to cleaning or disinfecting.
WARNING: To avoid electrical shock and damage to the system, remove the probe
battery or the probe adapter cable from the probe prior to cleaning or disinfecting.
WARNING: Disinfectants and cleaning methods listed are recommended by Siemens for
compatibility with product materials, not for biological effectiveness. Refer to disinfectant
label instructions for guidance on disinfection efficacy and appropriate clinical uses.
CAUTION: Do not sterilize probes using hot steam, cold gas, or Ethylene Oxide
(EO) methods. Before applying any other methods that might be recommended by
manufacturers of sterilization equipment, please contact your Siemens representative.
CAUTION: To avoid damage to the probe, do not immerse or allow the probe adapter
cable or connector of a probe to become wet.
CAUTION: The probes have been designed and tested to be able to withstand high level
disinfection as recommended by the manufacturers of approved disinfectant products.
Carefully follow the disinfectant manufacturer’s instructions. Do not immerse for more than
one hour.
CAUTION: Do not use abrasive cleaning agents, organic solvents such as benzene,
isopropyl alcohol, or phenol based substances, or cleaning agents containing organic
solvents to clean or disinfect probes. These substances can damage the probes.
CAUTION: Prior to cleaning or disinfecting a probe, you must remove the probe battery
and disconnect the probe adapter cable and remove the probe from the ultrasound
system. To prevent the probe cleaners or disinfectants from contacting and damaging the
ultrasound system surfaces, do not clean the probe on or near the ultrasound system.
Approved probe cleaners and disinfectants are not approved for use on the ultrasound
system surfaces. Unintended contact with approved probe cleaners and disinfectants can
result severe damage to the ultrasound system components.

Safety and Care
All probes should be cleaned and disinfected prior to their use on each patient.
Probe General Cleaning (including Low Level Disinfection):

Clean probes (including low level disinfection) after every patient use, including non-critical
applications. Do not allow body fluids, such as blood, to dry on the probe.
Routing cleaning steps are as follows:
1. Immediately after completing the exam, turn the probe off and remove the battery module.
Process the pieces separately.
2. Wipe the gel off the probe with a soft cloth.
3. Use a soft brush, sponge, or gauze pad lightly moistened in an enzymatic detergent such
as Metrizyme (in accordance with the manufacturer’s instructions) to remove all gel,
particulate matter, or bodily fluids from all components and surfaces. Carefully clean any
crevices, corners or seams.
4. Rinse with quality running water, and dry with a soft cloth or gauze pad.
5. Thoroughly examine and visually inspect all surfaces that have been cleaned to make
sure that they are clean. If visible debris is noticed, repeat Steps 3 and 4.
6. Immediately rinse the probe thoroughly with sterile water, then pat dry with a clean soft
cloth or gauze pad.
CAUTION: Do not run the probe Cable Adapter under water. Instead wipe with a lightly
moistened sponge or gauze pad.

Safety and Care
Probe High Level Disinfection
Preparation
Follow the Cleaning instructions above prior to high-level probe disinfection.
High-Level Disinfection
Soak the probe using a compatible disinfectant (listed below), following the manufacturer’s
instructions and specifications.
CAUTION: When disinfecting probes, be careful to immerse only the top portion of the
probe, up to two inches (5 cm) from the transducer face in the disinfecting solution. Do
not immerse the entire probe and do not immerse the battery pack, probe battery well, or
cable adaptor.
CAUTION: Strictly follow the instructions of the disinfectant manufacturer, and limit
the time probes are soaked to the minimum time recommended by the disinfectant
manufacturer. Follow the disinfectant manufacturer’s instructions for rinsing and drying
after disinfection.
CAUTION: Do not use strong solvents such as acetone, Freon, and other industrial
cleaners on transducers.
Probe Sterilization
CAUTION: The only sterilization methods compatible with ACUSON Freestyle probes
(including the probe battery pack) are those listed and described below. No other
sterilization methods should be used.
CAUTION: Carefully follow the instructions provided with the sterilization system.
CAUTION: Use treated water that is of a quality that ensures hard water stains do not
occur. Failure to remove all organic materials or detergents may result in the formation of
light-colored residue on the components. If residue is visible, you should clean, rinse, and
dry and re-sterilize the items prior to use.
Sterilization Preparation
Thorough and effective cleaning is essential to successful sterilization. Follow the Cleaning
instructions above prior to probe sterilization.

Safety and Care
Probe Sterilization: Sterrad

1. The probe main module and battery module must be keep disassembled from each other,
and packaged separately for sterilization.
2. Carefully inspect the modules for cleanliness and dryness prior to packaging for Sterrad
processing. If visible soil is present, the item must be re-cleaned and dried prior to
sterilization. If moisture is present, dry the item thoroughly prior to sterilization.
3. Place the dry battery module into an ACUSON Freestyle charging bay and charge the
battery fully before sterilizing.
The modules can be either wrapped or peel pouched in compatible material. Only
polypropylene wrap or Tyvek® pouches can be used in the Sterrad system.
If you choose to wrap, secure the package with Sterrad SealSure® Chemical Indicator
Tape.
4. Mark the tape or pouch used to package a battery with the expected expiration date of
the battery’s charge. (For a fully charged battery, it is advisable to recharge the battery if it
has been in a stored condition for over two months.)
If you choose to place items in a peel pouch, use a Sterrad Chemical Indicator Strip
marked with the expiration date of the battery’s charge placed on the inside of the pouch.
If the pouch has an imprinted indicator strip you may alternatively write the date here.
5. Follow your facility’s procedures for labeling sterilized items.
6. Process the items in the Sterrad system in accordance with its instructions. The probe
and battery modules have been validated with the following cycle parameters, for the
Sterrad models listed below:
Sterrad Model: Sterrad 100S

CYCLE DURATION
Pre-Plasma 10 minutes
Injection 6 minutes
Diffusion 2 minutes
Plasma 2 minutes
In the Sterrad 100S, two cycles of Injection/Diffusion/Plasma
are performed
7. Batteries can be used immediately or stored in accordance with your facility’s procedures.
8. Rotate stock and recharge and re-sterilize batteries, as necessary.
CAUTION: The probe Cable Adapter is not sterilizable.

Safety and Care
IPX8 Immersion Levels
CAUTION: To avoid damage to the probe, observe the continuous immersion levels
indicated for each probe type. When disinfecting probes, be careful to continuously
immerse only the top portion of the probe, up to two inches (5 cm) from the transducer
face in the disinfecting solution. The entire probe, battery pack, or probe battery will may
be immersed for short periods of time (under three minutes). Do not continuously immerse
the entire probe, battery pack, or probe battery well.
Example of continuous immersion level for each probe type
1. L8-3 probe (left)

2. L13-5 probe (middle)
3. C5-2 probe (right)

Safety and Care
Approved List of Disinfectants

The following matrix provides a list of approved disinfectants for all probes.
NOTE: The approved disinfectants, such as Cidex OPA, may discolor probe
housings, including the face of the probe. There is no associated degradation of
imaging performance or probe reliability.
Compatible Disinfectants for the System Console and Probe are listed below. Use of
disinfectants not listed may cause damage to the system and void the warranty.
System Console
Name Description
abcoCIDE 14 Gluteraldehyde
Asepti-Wipe Quaternary Ammonia
Cidex Gluteraldehyde
Cidex OPA Ortho-phthaldehyde
Cidex Plus Gluteraldehyde
MetriCide 14 Gluteraldehyde
T-Spray Quaternary Ammonia
T-Spray II Quaternary Ammonia
Probe
Name Description
Cidex Gluteraldehyde
Cidex Plus Gluteraldehyde
Wavicide-01 Gluteraldyhyde
Metrizyme Propylene glycol

Safety and Care
Caring for Probe Accessories

Instructions are provided for the accessories.
Probe Sheaths
WARNING: There have been reports of severe allergic reactions to medical devices
containing latex (natural rubber). Health care professionals are advised to identify latex
sensitive patients and to be prepared to treat allergic reactions promptly. For additional
information in the U.S.A., refer to FDA Medical Alert MDA91 1. In the United States of
America, for a single copy of a reference list on latex sensitivity write to LATEX, FDA,
HFZ-220, Rockville, MD 20857.
WARNING: To minimize the risk of cross contamination and infectious diseases, a sterile,
non pyrogenic probe sheath must be in place during procedures requiring sterility.
WARNING: Only a sterile probe sheath provides the sterile barrier required for surgical
procedures. To ensure sterility of a procedure, always place a sterile sheath on a probe,
as probes cannot be sterilized using hot steam, cold gas, or Ethylene Oxide (EO)
methods.
CAUTION: Siemens recommends that you follow all instructions provided by

manufacturers of sterile goods (probe sheaths) to ensure proper handling, storage, and
cycling of all sterile goods.
Using a disposable probe sheath on a probe reduces the possibility of cross contamination.
Always use a protective probe sheath when scanning an open wound or an area where the
skin is not intact.
Storage
WARNING: Before use, examine sterile goods, such as sheaths, for any material flaws.
Some packaging may list an expiration date. Any product showing flaws, or whose
expiration date has passed, should not be used.
CAUTION: Do not store probe sheaths in direct sunlight, as ultraviolet damage can
result.
Latex products have a limited shelf life, and should be stored in a cool, dry, dark place with an
ambient temperature between -5°C and +40°C and up to 80% relative humidity at +40°C.

Safety and Care
Recommended Use of the Probe Sheaths

Siemens makes every effort to manufacture safe and effective probes. You must take all
necessary precautions to eliminate the possibility of exposing patients, operators, or third
parties to hazardous or infectious materials. These precautions should be considered in the
use of any application that may indicate the need for such care, for example, when scanning
patients with open wounds.
Probe sheaths are single use items used to ensure proper acoustic coupling and provide
a prophylactic barrier for the intended ultrasound application. Sheaths are available for all
probes. Use only market cleared probe sheaths.
Application
WARNING: After placing the sheath over the probe, visually inspect the sheath to ensure
there are no defects. Do not use the sheath if it has any holes or tears.
WARNING: Carefully follow the labeling instructions provided with the probe sheath.
Disposal
While wearing protective gloves, remove the probe sheath from the probe and dispose of it
according to local, state, and regional regulations for biohazardous waste.

Safety and Care
Battery Safety
The ACUSON Freestyle contains rechargeable lithium ion batteries in the System Console.
These batteries are not accessible by the operator and may only be replaced or serviced by a
qualified service technician.
The ACUSON Freestyle probe also utilizes a rechargeable lithium ion battery. This is enclosed
in the removable battery pack.
To prevent the probe battery from bursting, igniting, or emitting fumes and causing personal
injury or equipment damage, observe the following precautions.
WARNING: Use only batteries supplied by Siemens Medical Solutions USA, Inc. with the
system and probe.
WARNING: Do not disassemble or alter the battery pack or remove the casing of the
pack.
WARNING: The battery contains safety circuitry and features. Do not disassemble or
alter the battery.
WARNING: Charge batteries only when the ambient temperature is between 0º and
40º C (32º and 104º F).
WARNING: Do not short-circuit the battery by directly connecting the positive and
negative terminals with metal objects.
WARNING: Do not heat the battery or discard it in a fire.
WARNING: Do not use a defective battery or a battery that appears to be malfunctioning

or not holding a charge. Replace such batteries.
WARNING: Do not expose the battery to temperatures over 60º C (140º F). Keep it away
from fire and other heat sources.
WARNING: Do not leave the battery in direct sunlight.
WARNING: Do not pierce the battery with a sharp object, hit it, or step on it.
WARNING: Do not use a damaged battery, or a battery pack with cracks or damage to
the casing.
WARNING: Do not solder a battery

Safety and Care
WARNING: The polarity of the battery terminals is fixed and cannot be switched or
reversed.
WARNING: Do not force the battery into its compartment in the probe.
WARNING: Do not connect the battery to an electrical power outlet.
WARNING: Do not continue to recharge a battery if it does not recharge properly after
two successive six hour charging cycles.
WARNING: If the battery leaks or emits an odor, remove it from all possible flammable
sources.
WARNING: Do not attempt to recharge non-rechargeable batteries, such as the batteries

included on printed circuit boards. Recycle non-rechargeable batteries according to local,
state, and regional regulations.
CAUTION: Remove the battery from the probe if the probe is not likely to be used for an
extended period. Prior to storage charge or discharge the battery to approximately 50% of
capacity.
CAUTION: To avoid the battery bursting, igniting, or emitting fumes from the battery and
causing equipment damage, observe the following precautions
CAUTION: Do not immerse the battery in liquid if it is damaged or the housing is cracked.
CAUTION: Do not immerse the battery in any liquid not listed in the chapter “Cleaning,
Disinfection, and Sterilization,” and do not submerge a battery beyond the time periods
specified in the instructions for recommended liquids.
CAUTION: If the battery emits an odor or heat, is deformed or discolored, or in any way
appears abnormal, immediately remove it from use.
CAUTION: Do not put the battery into a microwave oven or pressurized container.
CAUTION: Store the battery between 5º C and 60º C (41º and 140º F).
CAUTION: Use only Siemens-supplied batteries and charging devices.

Safety and Care
Good Ergonomic Practices

WARNING: The operation of an ultrasound system may to linked to musculoskeletal
disorders (MSDs).
In ultrasound imaging, ergonomics may be defined as the physical interaction between the
operator, the system, and the transducer, in the course of conducting exams. It is important for
the operator of the system to practice good ergonomic techniques to reduce the risk of injury.
This chapter is intended to provide guidelines to help you work more comfortably in order to
possibly reduce the risk of musculoskeletal disorders.
When using an ultrasound system, as with many similar physical activities, you may experience
occasional discomfort in your hands, fingers, arms, shoulders, eyes, neck, back, or other parts
of your body. If you experience symptoms such as constant or recurring discomfort, pain,
throbbing, aching, tingling, numbness, burning sensation, or stiffness, you should promptly
consult a qualified health professional. These may be symptoms of MSD. MSDs can be painful
and may result in potentially disabling injuries to the nerves, muscles, tendons, joints, or other
parts of the body. Examples of MSDs include carpal tunnel syndrome and tendonitis.
Steps you can take to guard against discomfort while scanning, or the risk of MSD are
described here. It is also recommended that you consult the guidelines of professional medical
societies concerned with ultrasound.
Interrupt Scanning
Interrupt scanning frequently, using breaks to rest and give soft tissue a chance to recuperate
from the strained positions and repetitive movements of examinations.
While scanning, avoid maintaining the same body position for extended periods of time, by
moving and varying head, neck, body, arm, and leg positions.
Positioning
Avoid bending or stooping.
Adjust the position of the ACUSON Freestyle such that viewing or reaching the controls does
not require strained or awkward body positions.
Whenever possible, use an adjustable chair with good back support, and adjust chair height to
promote good body posture. If possible, adjust the height of the patient bed to optimize body
posture.
Maintain a comfortable and balanced body position with minimal stress on your joints,
minimizing bending and twisting.
Keep elbows close to your side and relax your shoulders in a level position.
Hand and Wrist

Do not grasp the transducer with excessive force; hold it as lightly as possible.
Minimize the amount of pressure applied when pressing the transducer against the patient.
Avoid or minimize bending your wrist.
Exercise and Stretching

Targeted exercises and stretching may help avoid the risk of MSDs. Consult with a qualified
health professional to define a program suited to your needs and practices.

Safety and Care
Moving the System

The ultrasound system is a mobile unit. Before moving the system to another location, you
must prepare for the move by powering off and securing the system.
Unplug the power cord plug from the wall outlet. Pull on the plug, not the cord. Disconnect the
Ethernet cables from the ultrasound system.
Secure components such as the power cord, probes, and gel.
WARNING: When operating and transporting the ultrasound system using the ACUSON
Freestyle Rollstand, insure that the rollstand is configured according to the specifications
provided in this manual. Failure to do so can cause the system to tip over and create a
risk for injury to the user or patient and damage to the system.
WARNING: Do not tip the system in any direction more than 10 degrees. This action can
cause the system to tip over and create a risk for injury to the user or patient and damage
to the system.
WARNING: Preparations before moving the system are important to minimize potential
damage to sensitive components and to avoid safety hazards. Review the moving
instructions before moving the system.
WARNING: Do not park or leave the ultrasound system unattended on a slope. Even
when the brakes are engaged, the system may slide down a ramp.
WARNING: When using the system in a tabletop use, pull out the tilt stand on the rear of
the unit to position it securely. Make sure the stand is placed securely on an even surface
where the system will not be accidentally pushed.
CAUTION: When moving the ultrasound system, protect if from environmental changes
including : moisture, winds, dirt and dust, and extreme heat or cold exposure.
CAUTION: Avoid moving the ultrasound system on outside surfaces with loose dirt,
contaminants, or standing liquids.
CAUTION: Care should be taken to minimize shock and vibration of the ultrasound
system. Avoid uneven surfaces that contain an abrupt height change or jarring surface
irregularities.
CAUTION: After the move, make sure the ultrasound system has proper ventilation
during operation. Do not position the system against walls or hard surfaces that would
impede free ventilation around the system.
CAUTION: Do not allow linens, bedding, and/or hanging curtain partitions to block the
ultrasound system’s ventilation.
CAUTION: When moving the ultrasound system over longer distances, or shipping it,
place it in the protective shipping case provided by Siemens and pack it according to the
instructions.
CAUTION: When moving the ultrasound system over longer distances, remove probe
batteries from the probes.

Safety and Care
ACUSON Freestyle Rollstand Configuration
WARNING: Whenoperatingandtransportingtheultrasoundsystemusingthe ACUSONFreestyle

Rollstand, insure that the rollstand is configured according to the specifications provided
in this manual. Failure to do so can cause the system to tip over and create a risk for
injury to the user or patient and damage to the system.
Rollstand Configuration
1. Quick Release Adaptor Plate: the top of the plate should be placed no higher than
48 in/122 cm. Do not place anything other than the Freestyle, probe batteries, and probes
on this mount.
2. Handle: the top of the Handle should be placed no higher than 40 in/101 cm from the
floor.
3. Keyboard Shelf: should be placed no higher than 33 in/84 cm from the floor.
4. Rear Storage Basket: the top of the basket should be placed no higher than 30 in/76 cm
from the floor. Weight limit 4 lbs/1.8 kg.
5. Front Storage Basket: top of basket should be placed no higher than 24 in/61 cm from the
floor. Weight limit 4 lbs/1.8 kg.
6. Cable Wrap: should be placed no higher than 22 in/56 cm.
7. Video Printer Shelf: the shelf should be placed no higher than 12 in/30 cm from the floor.
Weight limit 6 lbs/2.7 kg. Secure printer with straps.

Safety and Care
System Upgrades
Performing System Software Upgrades

When performing system software upgrades, carefully follow the installation instructions that
accompany the software.
CAUTION: Back up or archive any patient studies that may be stored on the system prior
to performing a software upgrade.
CAUTION: Do not terminate power during a software upgrade or otherwise interrupt a

software upgrade. This may cause the system not to operate and may require system
servicing. When conducting a software upgrade, operate the system on AC Mains power
outlet and make sure the system battery is fully charged.
Consult your service representative or help desk contact with any questions you may have
regarding software upgrades.
Environmental Protection
Product Recycling and Disposal

Dispose of this product according to local, state, and regional regulations.
Batteries and electrical and electronic equipment can contain hazardous substances. If
released, the hazardous substances can harm people and the environment.
Siemens provides disassembly instructions to treatment facilities for the safe and proper
removal and recycling of electrical and electronic components in this product. For more
information, contact your local Siemens representative.
To the extent required by local laws and regulations, Siemens has programs for the return of
used products. For more information, contact your local Siemens representative.

Safety and Care
Recycling Batteries
WARNING: Never dispose of batteries by burning or by flushing into any waste water
system, for example, a lavatory. Compromising the structural integrity of a battery can
result in leakage or explosion and the potential for personal injury.
WARNING: Do not throw batteries into the trash. Collect and recycle used batteries
separate from other waste.
The system does not contain alkaline batteries. Printed circuit boards may contain lithium
batteries. If the system clock no longer keeps time, it could be time to replace the battery.
Contact your local Siemens representative.
Recycle batteries according to local, state, and regional regulations. Use a battery collection
program available in your country to recycle batteries.
To the extent required by local laws and regulations, Siemens will collect and recycle batteries
for this product at no charge. Contact your local Siemens representative for battery shipment
instructions.
Disposing of the Packaging Materials

Dispose of or recycle the packaging materials according to local, state, and regional
regulations.
To the extent required by local laws and regulations, Siemens will collect and dispose of
packaging materials for this product. For more information, contact your local Siemens
representative.

Safety and Care
Disposing of Components and Accessories
WARNING: Observe local, state, and regional regulations for the disposal of the
ultrasound system components and accessories.
Energy Conservation
For improved energy conservation when the system is not in use, power off the system. Keep
the system plugged into the power outlet.
For maximum energy conservation when the system is in storage, power off and unplug the
system from the AC Mains power outlet.
NOTE: Unplugging the system from the AC mains power outlet can shorten the life
of the system circuit board batteries.

Safety and Care
Technical Description
This Section provides a summary of important information regarding the specifications and
safe operation of the ACUSON Freestyle Ultrasound System. Read this entire User’s Manual for
important information on the safe installation and operation of the ACUSON Freestyle system, in
particular, the Safety chapter.
Upon request, Siemens Medical Solutions USA, Inc. will make available circuit diagrams,
component part lists, descriptions, calibration instructions, or other information that will assist
service personnel to repair those parts of the system which are designated by Siemens
Medical Solutions USA, Inc. as repairable by non-Siemens personnel.
ACUSON Freestyle Ultrasound System Technical Description

Manufacturer Siemens Medical Solutions USA, Inc.
685 Middlefield Road
Mountain View, CA 94043 USA
Electrical Power Requirements Input Voltage : 100 – 240 V
Frequency : 50/60 Hz
Current : 1.5 – 0.7 A
Fuse Rating : 250 V, 3 A
Fuse Type: 5 x 20 mm Slo-Blo
Classifications The ACUSON Freestyle is classified under IEC60601-1, UL 60601-1 as:
1. Class 1 protection against electrical shock. When probe and/or console are
operated from battery power, Class is Internally Powered Equipment.
2. For continuous mode of operation
3. Equipment not suitable for use in the presence of flammable anesthetic
mixture with air or oxygen or nitrous oxide.
4. System: Ordinary equipment without protection against ingress of water.
5. Probe: IPX8
6. Probe : Applied part Type B.
Environmental Conditions Indoor Use Only
Operating:
Temperature: 10º C to 40º C (50º F to 104º F)
Humidity (Relative Humidity): 10% to 75%
Pressure: 700 hPa to 1060 hPa (20.7 inHg to 31.3 inHg)
Transportation and Storage:
Temperature: –20º C to 60º C (–40º F to 158º F)
Humidity (Relative Humidity): 10% to 90%, Non-condensing
Pressure: 500 hPa to 1060 hPa (14.8 inHg to 31.3 inHg)
Physical Specifications Dimensions:
Console: 158 mm L x 373 mm W x 335 H
Probe: 153 mm L x 65 mm W x 34 mm H
Weight: 10.5 pounds (System and one probe with probe battery)
Batteries Probe battery reorder number: 11002304
Battery Performance
(Figures approximate and will vary with operating conditions)
Charge Time (empty to full): Probe battery = 2 hours / System battery = 5 hours
Run Time (full to empty): Probe battery = 1.5 hours / System battery = 1 hour
Number of charge cycles before charge capacity reduced to < 70% of original
capacity: Probe battery = 500 / System battery = 300

Setup
3 Setup
This section describes the functions of the Setup Menu that is used to specify system settings.
System Setup and Controls. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3

Overview of the Setup Menu. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3
How to Select Items from the Setup Menu. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-4
Setup Menu Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5
Scan . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5
Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5
Locating the Active Probe. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5
Connecting and Disconnecting Probes. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5
Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-6
User Exams. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-6
Network. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-6
DICOM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-6
System. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-7
Getting Help and Service Support . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-7
Closing the Active Page . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-7
Setting Image Controls. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-7
Removing Patient Information from Images. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-7
Administrative Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-8
Study List. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-9
New Patient Study. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-9
Close Study . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-9

Setup

Setup
System Setup and Controls

This section explains how to setup the system. The Setup Menu includes patient data entry
functions, patient study lists, system settings, and more.
Overview of the Setup Menu

To display the list of Setup options, press the SETUP Soft Key.
Location of SETUP Soft Key
Setup Soft Key Menu Options

Option Description
SCAN Activates the real-time imaging screen
PROBES Connect and disconnect probes using this option.
SETTINGS Manage system settings, including:
• User Exam profiles
• Network settings
• DICOM settings
SYSTEM Activate the System information page that provides
information about hardware and software configuration, and
installed options. Includes:
• Setting image controls
• Patient anonymity settings
• Administrative options
• Contact information for service
• Battery status
STUDY LIST Opens the list of studies.
NEW PATIENT STUDY Initiates data entry for a new patient study.
CLOSE STUDY Closes the active study.
Each option is described on the following pages.

Setup
How to Select Items from the Setup Menu

There are several ways to select an item from the SETUP menu list:
■■ Turn the large, outer Rotary knob to highlight an item, then turn the small, inner Rotary knob
to activate it.
■■ To move left/right, back/forth turn the inner Rotary knob.
■■ Use the Trackball which controls a pointer to highlight an option, and then touch the left
Trackball key to activate it.
■■ Use a compatible USB mouse for these controls (plug the mouse into one of the USB ports
on the I/O Panel; for more information see “Console Inputs/Outputs Panel” on page 1-5).
If an item in the Setup list has sub-pages, a pop-up window will display the additional choices.
Activate this pop-up window with the inner Rotary knob. The outer Rotary knob scrolls through
this list, and the inner knob activates a selection.
XXX
XXX
XXX
XXX
XXX
XXX
XXX
XXX
Xxxx
Xxxxxx
Xxxxxxxx Xxxx Xxxxx
Xxxxxx Xxxxxxx
Xxxxx Xxxx XXXXX XXXX
Xxx Xxxxxxx Xxxxx Xxxxxxx Xxxxxxxxxx
Xxxxx Xxxxx Xxxxxxxx
Xxxxxx
XXX XXX XXX XXX P S
Setup Menu and Sub-Menus; there are several ways to select items from the menus

Setup
Setup Menu Options

Scan
Activates the real-time imaging screen. When you are in a Setup page or menu the SETUP Soft
Key changes to SCAN.
■■ To go to the real-time imaging screen from a Setup page, select SCAN.
■■ To go to the real-time imaging screen when the Setup menu is displayed and Scan is
highlighted, turn the small Rotary knob.
Probes
The Freestyle Probes page is a list of the most recently used probes by Name (type of probe),
Serial Number and date Last Used.
Locating the Active Probe

If a probe is currently turned on and wirelessly connected to the system, pressing the IDENTIFY
Soft Key causes the probe to beep. This can be useful when trying to locate a probe. To stop
the probe from beeping, press the IDENTIFY Soft Key a second time.
NOTE: For the Identify function to operate, the probe must be: on, linked to the system, and within
range of the Bluetooth radio.
Connecting and Disconnecting Probes

■■ The CONNECT Soft Key connects the highlighted probe on the list if it is turned on and in a
three meter range of the console, or plugged into the system console using the probe Cable
Adapter.
■■ The DISCONNECT Soft Key terminates the connection to the active probe.
For a description of the routine method of connecting probes, see the Scanning and
Wireless Probe Operation chapters of this Manual.

Setup
Settings
The Settings options are used to configure the system:
■■ User Exams
■■ Network
■■ DICOM
User Exams
The ACUSON Freestyle comes pre-loaded with a variety of factory exam types (e.g., cardiac,
vascular). This option lets you create custom User Exams with the parameters and settings
that you specify. Note that a “u” preface identifies an Exam type as being user-defined.
For detailed instructions about Exam Types, see “Factory Exam Types” on page 4-7
and “User-Defined Exam Types” on page 4-8.
Network
The Network page includes information and the interface for establishing wired Ethernet or
wireless connections with the system.
For detailed instructions about Connectivity settings and configuration, see the
Connectivity chapter of this Manual
DICOM
The DICOM page includes information and the interface for establishing and managing
DICOM connections.
For detailed instructions about DICOM settings and configuration, see the Connectivity
chapter and the DICOM Conformance Statement of this Manual.

Setup
System
The System page provides access to information about your product’s hardware and software
configuration as well as installed options, including the following:
■■ Battery Status and Charge Levels for the system (console), left and right charger bays, and
the active probe
■■ System information including:
–– System serial number
–– Software version number
–– License number
–– Installed options
–– Subsystem circuit board information
■■ Image Controls (see “Setting Image Controls” and “Removing Patient Information from
Images”).
■■ Administrative Options: for more information see, “Administrative Options” on page 3-8.
Getting Help and Service Support

Press the HELPDESK Soft Key to enter contact information for your local Service support
representatives. Your Siemens Service Representative may access additional system
information from the Helpdesk page.
Closing the Active Page

To close the active page select the CANCEL option.
Setting Image Controls

Using the cursor and the Trackball, click on the slider tab using the left Trackball key to adjust
the following:
■■ Image Size: use the drop-down box to select the image size.
■■ Cine Playback: set the length of time of multi-frame cine loops played back in real-time
scroll memory.
■■ Monitor Brightness: move the slider bar to adjust the brightness of the monitor.
■■ Capture Quality: set the quality of JPEG-captured images.
–– For higher quality images, move the slider bar to the right.
–– For lower quality images, move the slider bar to the left.
Removing Patient Information from Images

The Study Anonymity option allows you to remove patient information from images saved
as either JPEG or DICOM. Make the scan anonymous by excluding either the Patient ID
(Identification), the Patient Name, or both. Default setting: the anonymizing features are
turned off; Patient Name and ID are displayed on saved images.
NOTE: These settings do not remove the Patient Name and ID from the DICOM data stored with the
study.

Setup
Administrative Options
The ADMIN Soft Key provides a list of administrative settings for the system as described in the
following table.
Admin Soft Key Settings

Option Description
Automatic Freeze When enabled, allows the system to freeze during real-time scanning when
imaging is inactive.
Clip Storage When enabled, allows “clips” to be saved.
Use the drop-down menu to set the length, in seconds, of the saved clips. Clips
of 10 seconds or longer will use a reduced Capture Quality setting.
Menu Time-outs When enabled, allows you to adjust the amount of time popup menus stay up
before automatically disappearing after inactivity.
Use the drop-down menu to set a faster or slower time.
Sleep Mode When enabled, allows the console to go into a power saving “sleep” mode
when inactive for a specified time.
Set the inactive time by selecting a time from the drop-down menu.
Probe Localization When enabled, allows the wireless probe tracking feature to operate. For more
information see, “Finding/Locating Wireless Probes” on page 6-11.
Probe Keys Lock When enabled, the probe keys will come up in a locked state during scanning.
This prevents control changes due to unintended hits of the keys. The console
will display a lock icon (a padlock) in the lower right corner of the system
console.
To unlock the keys: move your finger along the probe slider the length of the
slider up and then down OR press the probe’s plus key, then the minus key,
then the plus key (or the reverse: minus, plus, minus keys). Once unlocked,
after a period of inactivity, the probe controls will lock again.
Probe Middle Keys When enabled, allows the operation of the probe middle keys.
Print with Save When enabled, also makes a print when you select SAVE. This feature only
operates with compatible video printers like the Sony UP-D897.
Area Measurement - When enabled, uses the continuous trace method for area measurements.
Continuous Trace When disabled, uses the multiple point-to-point trace method.
Hide Image Settings When enabled, hides the image settings after a selected amount of time
after… following a controls change.
Set the time by using the drop-down menu.
Activate Scroll when Activates the Scroll key when image is frozen..
freezing
Use international Adds special characters to the on-screen keyboard.
keyboard
Language Select a language for the screen display using the drop-down list.
After changing the language, reboot the system to activate the new selection.
Date and Time • Adjust the date: Click on the Date field and select the day from the displayed
calendar.
• Adjust the time: Click on the up/down arrows to set the time. Check the AM/
PM checkbox to display time in 12-hour AM or PM mode; leave the box
unchecked for a 24-hour clock. The system is designed to automatically
adjust the date for leap years.
WARNING: The ACUSON Freestyle does not automatically adjust

for changes to and from daylight savings time. If and when your
locality changes the clocks to begin or end daylight savings time,
you will need to manually adjust the system time.
NOTE: Be sure to check the time and date displayed on the

system when you begin patient studies to make sure they are
correct.

Setup
Option Description
User Selected Keys Define shortcut keys that will appear in the Real-time Control bar.
Two B-Mode and one Color shortcut can be defined. The function of the Probe
middle keys can also be defined. Use the drop-down menus to specify the key
functions.
The Tools list can be used to access functions that are not specified for these
user-selected keys.
Mobile LInk When enabled, allows a Windows 8 mobile device running the Freestyle
Mobile Link App to connect to the system.
Study List
For details about the Study List, see the Patient Studies chapter of this Manual.
New Patient Study
For details about creating a New Patient Study, see the Patient Studies chapter of this
Manual.
Close Study
Closes the active study.


Patient Studies
4 Patient Studies
This section describes how to create patient records and view, manage, and export patient
studies.
Protecting Patient Health Information. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-3

About Patient Studies. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-3
Patient Study Fields. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-4
Patient Soft Keys. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-5
Creating New Patient Studies. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-5
Using Patient Information from a DICOM Server. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-6
Worklist Query. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-6
Study Exam Types. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-6
Factory Exam Types. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-7
User-Defined Exam Types. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-8
Creating a new User Exam Type . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-8
Updating a User-Defined Exam with New Settings . . . . . . . . . . . . . . . . . . . . . . . . 4-8
The Study List. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-9
Viewing the List of Patient Studies. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-9
Sorting the Study List. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-9
Scrolling through the Study List. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-10
Selecting Multiple Studies for Export or Deletion. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-10
Viewing Images in a Study from the Study List . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-10
Viewing Image Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-10
Managing Patient Studies. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-11
Exporting Patient Studies. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-11
How to Export Studies. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-11
Export Parameters. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-12
Editing Patient Studies. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-12
Deleting Patient Studies. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-12

Patient Studies

Patient Studies
Protecting Patient Health Information

Storing patient data on the ACUSON Freestyle only temporarily, and then archiving the data to
your institution’s secured archival systems can enhance protection of your patient’s Protected
Health Information (PHI).
WARNING: Protected Health Information (PHI) such as patient records, is subject to

privacy protection (such as is described in the US Health Insurance Accountability and
Portability Act and the European Union Data Protection Directive, 95/46/EC.) Health care
providers have a responsibility to protect PHI.
WARNING: Be aware that even a highly secured wireless network can be vulnerable to
unauthorized access.
About Patient Studies

Only one patient study can be active at a time.
A patient study remains open until you:
■■ close the current study,
■■ create a new study, or
■■ reboot the system.
To reactivate a closed study, select STUDY LIST, highlight the desired study then select Edit/
Open.
The most recent Institution entry in the Patient Study page is retained in memory. The
Institution name is displayed on the imaging screen.

Patient Studies
Patient Study Fields

To display the Patient Study fields press the SETUP Soft Key, then NEW PATIENT STUDY. When
entering data into the Patient Study field, the [OK] key confirms an entry. The study information
includes the fields described in the following table.
Patient Study Information Fields

Option(s) Description
Last Name, First Name, Patient name information.
Middle Name Note that the patient’s name can be removed from saved image scans using the
anonymity settings. For more information, see “Removing Patient Information from
Images” on page 3-7.
Patient ID A unique patient ID number.
NOTE: If you do not enter a Patient ID the system will generate one based on
time and date.
Birth Date To enter data, use the number keys.
Gender Select either Male or Female.
Exam Select an Exam Type from the drop-down list.
Height, Weight To enter data, use the number keys.
To display values using the metric system, click the Metric checkbox.
Accession Type text into the field.
Diagnosis Type text into the field.
Institution Select from the drop-down menu.
The Institution name is displayed on the real-time imaging screen.
Physician Select from the drop-down menu.
Operator Select from the drop-down menu.
Comments Enter any additional information or comments.
NOTE: Patient Name and ID fields are limited to 64 characters. If the field is too long to be completely
displayed on the real-time scanning screen, the entry will be shortened in the display and followed by
three dots.
NOTE: The system stores up to eight of the most recently used Institution, Physician, and Operator
entries.
When using an external USB keyboard, quickly pressing the following key combinations allows
you to enter special characters:
Press this key... then press this key Resulting character

‘ (apostrophe) a, c, e, i, n, o, u, y, z á, ć, é, í, ń, ó, ú, ý, ź
“ (quotation mark) a, e, i, o, u, y ä, ë, ï, ö, ü, ÿ
` (accent grave) a, e, i, o, u à, è, ì, ò, ù
~ (tilde) a, n, o ã, ñ, õ
^ (caret) a, e, i, o, u â, ê, î, ô, û
= (equals) a, o æ, œ
* (asterisk) a å
- (dash) a, i, o, u ā, ī, ō, ū
# (pound) c, s, z č, š, ž
. (period) e, z ė, ż
, (comma) c, e, i ç, ę, į
/ (slash) l, o ł, ø

Patient Studies
Patient Soft Keys
Patient Soft Keys

Soft Key Description
SCAN Returns to the scan screen.
CANCEL Closes the record without saving unconfirmed entries.
CLEAR Lets you start over by clearing information from all the fields.
WORKLIST Displayed if Worklist is configured for this system. For more
information see, “Worklist Query” on page 4-6.
Creating New Patient Studies

To enter Patient information:
1. Press the PATIENT Soft Key or select New Patient Study from the SETUP Soft Key menu
to display the New Patient screen.
2. Use the Trackball to place the cursor in each entry field, then press the left Trackball key
to open the on-screen keyboard. You can also place the cursor over the keyboard symbol
to the right of the entry box and press the left Trackball key to bring up the on-screen
keyboard. You can also use an external USB-compatible keyboard.
3. Save the new patient record, by selecting [OK].
4. To then go directly to the real-time imaging screen select Scan from the SETUP Soft Key
menu.
NOTE: If you start scanning a patient and save images without entering a patient name or ID, the
system will automatically create a Study file for that patient study. The patient name will be listed as
UNKNOWN, a machine-generated ID number will be created, and the date and time of the study will be
recorded. This information will become a part of the image screen saved with the images. During or after
the study, it is possible to modify the patient information that appears in the Patient Study Archive.
NOTE: If a patient already has a study stored in the system, you will still need to enter new patient
information at the time of a new study; the system does not provide patient folders with multiple studies.
NOTE: If the on-screen keyboard does not automatically activate as expected and you have a USB
mouse or a wireless USB mouse connected, disconnect the USB mouse or use the pointer to select the
on-screen typewriter symbol to activate the on-screen keyboard.

Patient Studies
Using Patient Information from a DICOM Server

If your system has the Worklist option and is configured and connected to a DICOM server you
can obtain existing patient information (for more information, see “Overview of Connectivity” on
page 8-3).
Worklist Query
This option provides a shortcut to entering patient information as you create new patient
studies by accessing your DICOM Worklist Server (where patient information can be stored).
You can query the Worklist server using a variety of search terms or conditions, such as
patient name or exam date. If the query returns a patient for whom you want to create a study,
highlight the patient name in the response list, and select Create Study for this Patient. The
data will be entered into the system and the study will be activated for that patient.
To access the Worklist server use the Soft Keys, SETUP / SETTINGS / DICOM / WORKLIST.
Study Exam Types

There are two kinds of study Exam types:
■■ Factory/Standard exam types
■■ User-created exam types
You can change the Exam Type during scanning using the Exams key in the real-time control
window.
You can also specify which Factory/Standard Exam Types are available during scanning:
1. Select SETUP / SETTINGS / USER EXAMS.
2. Click the [+] box to display the lists of Exam types; to hide the lists, click the [–] box.
3. Use the checkboxes to select the desired Exam types.

Patient Studies
Factory Exam Types

The factory Exam Types provide real-time parameter presets optimized for specific types of
exams (for information about creating user-defined exam types see “User Exams” on page
3-6). These standard exam types can help optimize imaging settings with minimal effort.
Factory Exam Types are shown in the following table listed in alphabetical order. On the system
they are displayed in the most-recently-used order.
Exam Types are organized in the following groups: Abdominal, General, Musculoskeletal,
Nerve, Obstetrics/Gynecology, Small Parts, and Vascular.
Factory Exam Types

Screen Display Description
Abd Deep Abdominal Deep
Abd Gen Abdominal General
Abd Vasc Abdominal Vascular
Abd Renal Abdominal Renal
General General
MSK Deep Musculoskeletal Deep
MSK Elbow Musculoskeletal Elbow
MSK Foot/An Musculoskeletal Foot/Ankle
MSK Gen Musculoskeletal General
MSK Hand/Wr Musculoskeletal Hand/Wrist
MSK Hip Musculoskeletal Hip
MSK Knee Musculoskeletal Knee
MSK Shouldr Musculoskeletal Shoulder
MSK Spine MSK Spine
MSK Sup Musculoskeletal Superficial
MSK Tendon Musculoskeletal Tendon
Nerve Deep Nerve Deep
Nerve Gen Nerve General
Nerve Spine Nerve Spine
Nerve Sup Nerve Superficial
OB/Gyn Gyn Obstetrics/Gynecology Gynecology
OB/Gyn OB Obstetrics/Gynecology Obstetric
SP Breast Small Parts Breast
SP Deep Small Parts Deep
SP Gen Small Parts General
SP Sup Small Parts Superficial
SP Thyroid Small Parts Thyroid
V Arterial Vascular Arterial
V Carotid Vascular Carotid
V Gen Vascular General
V Vn Diff Vascular Venous Difficult
V Vn LwExtr Vascular Venous Lower Extremity
V Vn Sup Vascular Venous Superficial
V Vn UpExtr Vascular Venous Upper Extremity

Patient Studies
User-Defined Exam Types

User defined Exam Types are preceded by “u”. You can create up to 64 different user exams.
The User Exam page displays the list of User Exams that have been created, including the
real-time settings by Probe type.
Display the list of User Exams that have been created on the User Exams page:
1. Press the SETUP Soft Key.
2. Select the SETTINGS option.
3. Select USER EXAMS.
You can display real-time settings by Probe type and create your own Exam Type with the
system settings you prefer.
User Exam Soft Keys:
■■ DELETE: deletes User Exams from the system.
■■ RENAME: allows you to edit the name of the User Exam; names are limited to nine
characters.
■■ ACTIVATE: makes the highlighted Exam the active Exam Type.
Creating a new User Exam Type

1. During real-time scanning, select one of the pre-loaded factory Exam Types — not a User
Exam Type; User Exams are prefaced with the letter “u” (for example, “u Cardio1”).
2. Change the system real-time control settings, such as Depth and Gain, that you prefer for
the exam type you are creating.
3. When you have specified the settings you want, touch the Exams Soft Key, then select
Save Exam. The settings will be saved with the name “u Exam” followed by a number.
You can then rename the Exam in the SETUP / SETTINGS / USER EXAMS page.
NOTE: If you are unable to create new User Exams, you may have exceeded the number of User
Exams the system allows. The system stores a total of 64 User Exams. Delete unused User Exams so
new ones can be created.
Updating a User-Defined Exam with New Settings

1. During real-time scanning, use the Exams Soft Key to activate the User Exam you want to
update.
2. Change any of the control settings (e.g., Gain, Depth).
3. Select Save Exam.
For information about saving images to a Patient Study, see the Scanning Chapter.

Patient Studies
The Study List

The Study List includes all the patient study files that have been imaged and stored on the
system. You can view studies from this list and send them (using the Export function) to a
storage device such as a USB drive, or to a network destination such as a DICOM picture
archival system (PACS).
Viewing the List of Patient Studies

To access the Study List,
1. Press the SETUP key.
2. Select STUDY LIST from the menu.
The Study List displays the studies in a tabular form, with column headers for Patient name,
exam date, Patient ID, and export status. If a study has been archived (exported) to an external
storage location an arrow appears next to the study. The study storage memory used symbol
indicates the percentage of memory that has been used.
Scan Delete Edit Export 3
The Studies List screen
1. List of studies
2. Thumbnail images from the highlighted study
3. Study Storage Memory Used symbol
Sorting the Study List

The default is to show studies sorted by their study date.
To change the sort to a different category, click on a column header.

Patient Studies
Scrolling through the Study List

To scroll through the study list, use the outer Rotary knobs.
If a study contains saved images they are displayed as thumbnails. The inner knob highlights
the images and allows you to view them full size.
To return to scrolling through the Study List, turn the inner knob so the thumbnail image is no
longer highlighted.
Selecting Multiple Studies for Export or Deletion

To select multiple studies for exporting or deleting place the pointer in the space to the left
of the name and press the left Trackball key. The selected studies will be marked with a
checkmark (). To de-select, place the pointer over the checkmark and press the left Trackball
key.
Viewing Images in a Study from the Study List

If a highlighted study has saved images, thumbnail versions of the images will be displayed at
the right of the screen. To highlight an image, turn the small Rotary knob one click. To view the
image in View mode, turn the small Rotary know a second time.
Viewing Image Controls

The VIEW Soft Key opens all the recorded clips from the active study. Studies may also be
viewed by selecting them from SETUP / STUDY LIST.
When viewing study images:
■■ Next cycles through the stored clips.
■■ PANEL view displays multiple images on the same screen; then use these controls:
–– MORE makes thumbnails smaller
–– FEWER makes thumbnails bigger
–– DELETE highlight and delete selected thumbnails
■■ DELETE removes the highlighted clip from the study.
Studies
 Name Date Id
Smith, John 05-FEB-2013 2013.02.0546
 Jones, Jane 05-FEB-2013 2013.02.0545
Abbot, Steven 05-FEB-2013 2013.02.0544
 White, Emma 05-FEB-2013 2013.02.0543
Patient, F 05-FEB-2013 2013.02.0542

Patient, E 05-FEB-2013 2013.02.0541
Patient, D 05-FEB-2013 2013.02.0540
Patient, C 05-FEB-2013 2013.02.0539  
Patient, B 05-FEB-2013 2013.02.0538  
Patient, A 05-FEB-2013 2013.02.0537  
Scan More Fewer Delete Scan More Fewer Delete
Panel views of study thumbnail images; left picture: fewer, larger thumbnails; right picture: more, smaller thumbnails

Patient Studies
Managing Patient Studies
Exporting Patient Studies

The Export function sends selected studies to a storage medium (on a network or a compatible
USB drive).
How to Export Studies

To export patient studies, follow these steps:
1. Be sure you have the desired type of export hardware connected, e.g., a USB drive or a
configured DICOM network.
2. Open the study list by selecting STUDY LIST from the SETUP menu.
3. Select a study by placing the cursor over the checkbox to the left of the study and
pressing the left Trackball key to check or uncheck the box. To export multiple studies at
one time, check multiple boxes.
4. Press the EXPORT Soft Key.
5. Specify the Configure Export choices (see “Export Parameters” on page 4-12).
6. Click [OK] to begin the export. While the export is taking place, the Export List shows
details about the study being exported and the status of the export, indicating how many
clips have been stored out of the total. To terminate the export, click [CANCEL].
NOTE: Allow the status indication to complete and show no additional clips to store
before removing the USB drive, otherwise the export may not be successful.
When a study has been successfully exported, a curved arrow symbol is displayed to the right
of the study.

Patient Studies
Export Parameters
Pressing the EXPORT Soft Key opens the Configure Export list with the following fields:
■■ Export Format: choose an export format: DICOM Network, DICOM Media, DICOM Media
DSF (Decompressed Single Frame), or PC Viewable. DICOM Media and PC Viewable are
used to store studies to a compatible USB external drive connected to the system. If no
drive is connected, these options are not displayed.
■■ Storage Destination: for detailed information see the Connectivity chapter of this Manual.
■■ Storage Commitment Destination: for detailed information see the Connectivity chapter of
this Manual
Editing Patient Studies

2. Press the EDIT Soft Key to activate the Studies page where you can edit patient
information (name, birth date, etc.).
NOTE: Patient ID cannot be edited.
Deleting Patient Studies

The Delete function removes studies from the system.
2. Highlight a study in the Study List and press the DELETE Soft Key.
You will be prompted to confirm that you intend to delete the study before it is removed.
If you intend to archive a study to an external storage medium, do not delete the study prior to
the archival being performed. Once a study has been deleted, it cannot be recovered from the
system.
CAUTION: Confirm that an archival operation has been successful before deleting a
study from the system.

Scanning
5 Scanning
This section describes the real-time scanning operation.
Using the Probe. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3

About the Probe. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3
Probe Orientation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3
Overview of the Probe. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3
Probe Controls. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-4
Locking and Unlocking the Probe. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-4
Probe Shortcuts for Save and Color. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-4
Connecting the Probe . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-5
Cabled Probe Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-5
Wireless Probe Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-6
Connecting More Than One Wireless Probe . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-6
The Real-Time Scanning Screen. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-7
Overview of the Scanning Process. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-8
Real-Time Scanning Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-9
Selecting an Exam Type from the List of Exams . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-10
Freezing an Image. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-10
Scanning Soft Keys . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-11
B-Mode Scanning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-12
B-Mode Tools. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-12
Color Flow Mode Scanning. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-13
Color Flow Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-13
Measurements. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-14
Performing a Measurement. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-14
Deleting Measurements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-14
Ellipse Measurement. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-14
Area Measurement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-15
Adding Text Annotations to Studies. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-16
Text Functions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-16

Scanning

Scanning
Using the Probe
About the Probe

Probe Orientation
The probe index marker is the side of the probe where the probe on/off symbol is located. This
corresponds to the ACUSON “a” symbol next to the image display. The probe model numbers,
such as “L8-3” also serve as index markers. For transducers in non-cardiac applications, the
normal and default location of the on-screen index marker symbol is to the left of the image.
Overview of the Probe
Controls on the probe include a slider, plus/minus keys, middle keys
1. Back of probe
2. Circular plus/minus keys and slider bar
3. Probe middle keys
4. Front (or “face”) of probe
NOTE: In wireless mode, press the two on-probe circular keys continuously to turn
the probe on and off (see “Wireless Probe Operation” on page 5-6).

Scanning
Probe Controls
Functions in the real-time Control Bar can be adjusted or selected using the controls on the
probe. These controls include the slider, the two circular buttons, and the two buttons in the
middle of the probe.
The slider mimics the function of the large Rotary knob on the console, moving the selection of
the active item in the real-time control knob:
■■ To move the highlight up the list, push upward on the slider, away from the transducer face.
■■ To move the highlight down, push downward on the slider, toward the transducer face.
The button towards the rear of the probe (away from the transducer) represents Plus, the
button towards the front of the probe (towards the transducer) represents Minus. These mimic
the functions of the inner Rotary knob on the console.
■■ Plus corresponds to clockwise rotation of the knob.
■■ Minus corresponds to counterclockwise rotation of the knob.
Locking and Unlocking the Probe

Before using the probe controls, you may have to unlock these functions on the probe if you
unchecked the Enable Probe Key and Slider selection in the SETUP / SYSTEM / ADMIN page.
NOTE: When the probe is locked, a padlock icon is displayed on the bottom right of
the console screen.
There are two ways to unlock the probe:

■■ Slide the probe slider the length of the slider in both directions
■■ Press the plus key, then the minus key, then the plus key (or the reverse)
Once unlocked, the controls will lock again after a period of inactivity.
Probe Shortcuts for Save and Color

The two keys in the middle of the probe can be used as shortcuts for the function you select on
the System Administration page. Tap either probe key three times to activate the function.

Scanning
Connecting the Probe

There are two ways to operate the probe with the system:
■■ Cabled
■■ Wireless
Cabled Probe Operation

To operate the probe with the removable probe Cable Adapter, plug the probe cable into the
system I/O panel (see “Console Inputs/Outputs Panel” on page 1-5), and insert the probe end
into the probe.
NOTE: Both ends are keyed to prevent improper connection. Do not use force to
connect either end of the cable.
During cabled probe operation, the probe comes up with the image frozen. Select Unfreeze to
go to real-time scanning.
NOTE: If a probe is already connected using the probe Cable Adapter you cannot
connect another probe using the wireless connection. To make a wireless probe
connection, unplug the probe Cable Adapter at the probe or system console.

Scanning
Wireless Probe Operation

To operate the system probe in wireless mode, insert a charged probe battery pack into the
probe.
NOTE: The battery pack is keyed to prevent improper connection. Do not use force
when inserting the probe battery pack.
Probe and battery; line up battery connectors with probe connectors
With the system power ON, turn the probe on by continuously pressing the two circular on-
probe buttons. When power has been turned on for the probe, you will hear a beep from the
probe. The system and the probe will automatically connect.
Connecting More Than One Wireless Probe

To use more than one probe in wireless mode during an exam:
1. Turn the first probe off by continuously pressing the two circular on-probe buttons, thereby
disconnecting it from the console.
2. Connect to the second probe.
NOTE: If a Probe is connected to the console with the probe Cable Adapter, you
will need to disconnect it to make a wireless connection to another probe. You can
disconnect it either at the probe or the console end.

Scanning
The Real-Time Scanning Screen
4
5
XXX
L13-5
Nerve Gen XXX
2.5cm
G 9
CG 10
XXX
SC 3
SF 6 XXX
PP 10
1 55dB
CF 1 XXX
CP 1
Vel 1
Pri 4
XXX
20 Hz
XXX
XXX
ANL 0.0 dB
XXX XXX XXX XXX

2 P S
Real-time Scanning
1. Imaging Area
2. Soft Keys
3. ANL: Average Noise Level. A measure of wireless probe signal quality. See the Wireless
Probe Operation chapter of the Manual for details about ANL.
4. Real-time Control Bar Soft Keys: touch the control bar to activate the Soft Key next to the
bar (e.g., Freeze, Save, etc.).
5. The on-screen settings window is the area next to the image that displays the settings of
controls including depth, gain, probe type, exams, etc.

Scanning
Overview of the Scanning Process

Scanning is controlled using the Soft Keys, real-time Control Bar, and Rotary knobs.
Basic steps to complete a scan and save it to the Study List:
1. Press the console power button to turn the system on and allow it to boot up.
2. To enter a new Patient Name and create a new Patient Study, press the PATIENT Soft
Key or SETUP / NEW PATIENT STUDY, then use the on-screen keyboard or an external
keyboard to enter the patient Name, ID, etc (see “Creating New Patient Studies” on page
4-5).
3. Select an Exam Type (see “Study Exam Types” on page 4-6).
4. Press the SETUP / SCAN Soft Key to go to scanning mode and start imaging.
5. Make sure your probe is connected (either cabled or wirelessly) and turned on. To turn a
probe on for wireless operation, press the probe Plus and Minus keys continuously until
you hear the probe beep.
6. Make any adjustments using the real-time Control Bar Soft Keys.
7. Press the Freeze key to freeze an image.
8. Press Save to save frames or clips.
9. If desired, press the MEASURE Soft Key to make measurements (see “Measurements” on
page 5-16).
10. Press the VIEW Soft Key to view saved frames or loops.
11. To export studies to an external drive or system, see “Exporting Patient Studies” on page
4-11.
12. To view a list of completed studies press SETUP / STUDY LIST (see “The Study List” on
page 4-9).

Scanning
Real-Time Scanning Controls

The Real-time Control Bar along the right side of the screen provides Soft Keys for the
functions described in the following table.
The larger, outer Rotary knob moves up or down the list, highlighting an active control. The
smaller, inner Rotary knob adjusts the settings of the highlighted function. The probe controls
also provide these functions. Additionally, the controls may be activated by pressing the button
area next to the control on the front panel.
Real-Time Scanning Controls

Real-time Control Bar Keys Description
Freeze/Unfreeze Freezes and unfreezes the image. When the image is frozen, the light
on the probe will flash on and off.
When you press Freeze during real-time scanning, you can select
Scroll and use the inner Rotary knob or probe keys to step frame-
by-frame through the image memory. The scroll memory is the
immediate sequence of frames that were produced just prior to the
freeze.
The Cine key plays the scroll memory in a repeating loop.
Save Stores a still-frame image to the Patient Study file in internal memory.
NOTE: During live scanning a circular symbol appears in the
upper right corner of the screen for the length of time the Save
or Clip is taking place. A new Save or Clip cannot be started
until the Save or Clip is completed.
NOTE: If you select Save or Clip and the system does not
have any study storage memory available, the study storage
memory used symbol will appear showing 100%. Delete studies
to make memory available.
Clip Stores a multi-frame image clip to the Patient Study file in internal
memory. In order for clips to be stored, the Enable Clip Storage
checkbox on the Setup/System/System Admin page must be
checked.
NOTE: During live scanning a circular symbol appears in the
upper right corner of the screen for the length of time the Save
or Clip is taking place. A new Save or Clip cannot be started
until the Save or Clip is completed.
NOTE: If you select Save or Clip and the system does not
have any study storage memory available, the study storage
memory used symbol will appear showing 100%. Delete studies
to make memory available.
Gain Adjusts the overall image gain.
Displayed in the on-screen settings window as G.
Depth Adjusts the scanning field of view. Scale markers in centimeters are
displayed along the edge of the image. In the on-screen settings
window, the bottom depth number is displayed in centimeters.
Note that for linear array probes, distance markers are also shown
along the top of the image and the center of the probe is marked with
an arrow.
When making changes to the depth setting, the displayed depth
setting number turns blue until the actual image depth changes to the
new setting.
Color Turns color flow mapping on and off. The region of interest is moved
up or down with the Color Box Soft Key.
Displayed in the on-screen settings window as C Box.
N Gain Adjusts the near field gain.
Displayed in the on-screen settings window as NG.
Tools Activates the Tools menu for additional image adjustment.
Exams Displays the list of factory and user-defined Exam Types.
For more information, see “Selecting an Exam Type from the List of
Exams” on page 5-11.

Scanning
Real-time Control Bar Keys Description

TGC (Time Gain Activates keys for Near, Mid, and Far Gain controls. “Auto” restores
Compensation) default settings and “Exit” closes the TGC control list.

Scanning
Selecting an Exam Type from the List of Exams

Pressing the Exams Soft Key on the Real-time Control Bar displays a list of factory Exam
Types and user-defined Exam Types that you can select from. Exam types provide presets of
system controls in order to simplify optimization of images for different applications and patient
types. See the Setup and Patient Studies chapters for more information regarding Exam Types.
Pressing Exams displays the following buttons in the real-time control window:
Exit Exams – exits the Exam list.
Save Exam – saves the current control settings as a user-defined exam. This can be viewed
and edited in the Setup/Settings/Exams page.
User-defined exams are shown with the letter “u” in front of the name.
Page – steps through multiple pages of Exam Type lists if there are more than can be displayed
in the real-time control window.
Exam Types (e.g., Vascular, Abdominal) – the list of Exam Type groups are in the most-
recently-used order. Selecting an Exam Type group will display the individual Exam Types
available for that group.
Freezing an Image
When you press the Freeze Soft Key during real-time scanning, the current image freezes. Use
the following Control Bar options:
Save – saves the current image.
Scroll – use the inner Rotary knob or probe keys to step frame-by-frame through the image
memory. The scroll memory is the immediate sequence of frames that were produced just prior
to the freeze.
Cine – plays the scroll memory in a repeating loop.
Tools – displays the Tools sub-menu (see “B-Mode Scanning” on page 5-13 and “Color Flow
Tools” on page 5-15).
Text – lets you add text to an image (see “Text Functions” on page 5-18).
Print – makes a print of the image. This feature only operates with compatible video printers
like the Sony UP-D897.

Scanning
Scanning Soft Keys

The four Soft Keys along the bottom of the screen are controlled by the four circular buttons on
the system console. They are described in the following table.
Scanning Soft Keys

Soft Key Description
SETUP Displays the Setup page.
PATIENT Displays the New Patient data entry page.
MEASURE Displays the Measurement tools.
VIEW Opens all of the recorded clips from the active study. Studies may also be viewed
by selecting them from SETUP / STUDY LIST.
When Viewing study images:
• To cycle through the stored clips, press Next on the real-time Control Bar.
• To display multiple thumbnail images on the same screen press the PANEL
Soft Key.
- To display a larger number of thumbnails, press MORE.
- To display a smaller number, press FEWER.
- To display the highlighted clip in full-screen mode, turn the inner Rotary knob
or press the probe key.
• To review stored clips, select Play; to stop the playback, select Pause.
• To delete a clip from the study, highlight the clip then press DELETE.
• To display the Study List, press LIST.

Scanning
B-Mode Scanning
The default scanning mode for the system is B-Mode.
NOTE: Functions listed in the Tools menu will vary depending on how the System
Administration / User Selected Keys are configured.
B-Mode Tools
The real-time Control Bar Tools Soft Key displays a number of secondary-level real-time
imaging-related controls. The active Tools items will vary according to the scanning mode.
Press the Tools button to display the Tools options. When this list is active, the Rotary knobs
will control interaction with the list. Use the knobs in the same manner as is used to control the
real-time control bar. The outer knob moves up and down the list and the inner knob adjusts
the value or state for individual items.
B-Mode Tools Sub-Menu

B-Mode Tools Sub-Menu Description
Exit Tools Exits the Tools sub-menu.
PostProc Post Processing. Adjusts the gray scale curves of the B-mode
image. Lower values will have softer appearance, higher values will
have a more “contrasty” appearance.
Displayed in the on-screen settings window as PP.
Dyn. Range Image Dynamic Range. Displayed in decibels (dB).
Displayed in the on-screen settings window as numerical units
followed by dB.
Compound Spatial Compounding. Selects different levels of spatial
compounding. Spatial compounding combines different scan steering
angles to improve image quality.
Displayed in the on-screen settings window as SC.
Speckle Speckle Filter. Applies image filters that remove speckle or enhance
edges. In general, higher values will apply more filtering for potentially
smoother image appearance.
Displayed in the on-screen settings window as SF.
L/R Reverse Left/Right Reverse. This switches the orientation of the image on the
screen so that the index marker symbol display is moved from the left
of the image to the right of the image.
M-Line Displays a dotted line through the middle of the image with depth
markers.
Needle Visualization Improves the display of needles during procedures. See below for
details.
Wide Widens the image of linear probes.


Scanning
Needle Visualization
This setting improves the display of needles during procedures by brightening linear structures,
such as needles, when they are perpendicular to steered frames activated by the user.
It adjusts the system’s spatial compounding function to emphasize steering angles that may
improve the display of needles. It also adjusts other image parameters, such as speckle filter,
for this purpose.
If you specify Needle Visualization as one of your User Selected Keys in the System
Administration settings (see “Administrative Options” on page 3-8), Needle V will be a
dedicated key in the Real-time Control bar, and will not be listed in the Tools menu.
When the Needle V key is active it has six settings (the default setting is OFF). Turn the small
knob or select the “+” or “-“ button on the probe to pick a setting:
■■ ON: needle entering from the side of probe with the index marker, with steep angle.
■■ ON: needle entering from the side of probe with the index marker, with shallow angle.
■■ OFF
■■ ON: needle entering from opposite the side of probe with the index marker, with shallow
angle.
■■ ON: needle entering from opposite the side of probe with the index marker, with steep
angle.
■■ ON: needle enhancement without steering angle.
When one of the ON settings is active, a graphic overlay will appear on the image. The dotted
line through the image approximates the steered angles active for that setting for brightening
the display of a needle. For optimal display, the needle would be on a path that is perpendicular
to this dotted line. Other linear shapes in the image that are perpendicular to this line, may also
appear brighter.
Press the system console Needle V key to turn the most recently used Needle Visualization
setting ON and OFF. If you specify Needle Visualization as the User Selected Key for the
Probe middle keys, pressing either of the Probe’s middle keys three times will also turn the
most recently used Needle Visualization setting ON and OFF.
NOTE: Needle Visualization can also be used in Color Flow mode.

Scanning
Color Flow Mode Scanning

Pressing Color on the real-time Control Bar activates color flow mapping mode. This key
switches color flow on and off.
In color flow mode the real-time controls include:
C Gain – Color Gain controls the color flow overall gain.
C Box – Color Box controls the up/down position of the color flow box.
Color Flow Tools

The real-time Control Bar Tools Soft Key displays a number of secondary-level real-time
imaging-related controls. The active Tools items will vary according to the scanning mode.
Press the Tools button to display the Tools options. When this list is active, the Rotary knobs
will control interaction with the list. Use the knobs in the same manner as is used to control the
real-time control bar. The outer knob moves up and down the list and the inner knob adjusts
the value or state for individual items.
Color Flow Mode Tools Sub-Menu

Color Flow Mode
Tools Sub-Menu Description
Exit Tools Exits the Tools sub-menu.
Color Map Steps through multiple color flow maps. This selection also allows you to move from
velocity mode to power mode.
They are displayed in the on-screen settings window as either Vel (velocity maps) or Pwr
(Amplitude Power maps). The maps are represented in the color bar next to the real-time
image.
Vel Invert Velocity Invert. Shifts the color map orientation from the default of red = towards the
transducer, to blue = towards the transducer. When invert is selected, the color map
graphic bar will invert.
Displayed in the on-screen settings window as Vel.
WARNING: It is important to pay careful attention to the color flow invert

status of the system. The non-inverted state is red=towards the transducer,
displayed at the top of the color bar and blue=away from the transducer,
displayed at the bottom of the color bar.
Priority Adjusts the arbitration that takes place between B-Mode tissue signals and Color Flow
mapping signals. Higher priority settings will give greater weight to color flow signals. This
can be used with weaker flows or to fill in flow near vessel borders.
Displayed in the on-screen settings window as Pri.
C Persist Color Persistence. Increases or decreases the amount of persistence applied to Color
Flow signals. Higher settings will produce a smoother looking image and may help with
weak flow, but may have an appearance of lower frame rates.
Displayed in the on-screen settings window as CP.
C Filter Color Filter. Adjusts the Color Flow high pass filter. Lower settings will pass through
lower frequency flow signals.
Displayed in the on-screen settings window as CF.
C Scale Color Scale. Increases or decreases the Color Flow pulse repetition frequency. The
scale is displayed next to the color bar in centimeters per second.


Scanning
Measurements
Performing a Measurement
The measurements function can be performed from real-time scanning or starting with a frozen
image. Up to ten individual measurements can be made on an image.
To perform measurements on an image:
1. Press the MEASURE Soft Key. The image will freeze and the measurement choices will
appear in a menu above the key.
2. Use the Rotary knobs to make your selection, highlighting the item with the outer knob,
and activating it with the inner knob.
3. When you select DISTANCE, a cross-hair cursor will appear on the screen. Place this at
the starting point using the Trackball, then press the left Trackball button.
4. Use the Trackball to place the cursor at the endpoint, then press the left button again
to complete the measurement. During the drawing, you can reverse direction using the
Trackball to back up and delete parts of the trace. The numerical result is shown next to
the drawing.
5. Press Save to save an image with measurements.
Deleting Measurements
Press DELETE to delete the last completed measurement.
To skip to an earlier measurement for deleting, use Next.
To delete all measurements, press DELETE ALL.
Ellipse Measurement
To perform an ellipse measurement:
1. Activate the ellipse function by selecting ELLIPSE from the MEASURE sub-menu. This
brings up a cross-hair cursor you can position with the Trackball at the area of interest.
2. To display the ellipse form, press the left Trackball button. With the cursor inside the
ellipse, press the left button continuously and use the Trackball to reposition the ellipse.
3. To change the size or shape of the ellipse, place the cursor well outside of the ellipse and
press the left button continuously use the Trackball to change the shape or size of the
ellipse, moving the cursor to different positions around the ellipse to do so.
4. When you have finished, double-click the left Trackball button to complete the
measurement.
NOTE: It is possible to perform measurements on images being viewed from the
Study List, but the measurements cannot be saved in this case.

Scanning
Area Measurement
To perform an area measurement:
1. Activate the Area function by selecting AREA from the MEASURE sub-menu.
2. Position the cross-hair cursor at the starting point by pressing the left Trackball button.
NOTE: If you have selected the continuous trace method in the SETUP / SYSTEM /
ADMIN page, use the Trackball to trace the area.
3. While drawing you can reverse direction using the right Trackball key to back up and
delete parts of the trace. If you have selected the point-to-point method in the SETUP /
SYSTEM / ADMIN page (by disabling Continuous Trace), use the Trackball to position the
cursor, and the left Trackball button to set multiple points.
4. To complete the measurement, leave at least a small gap between your finishing point
and the starting point, and press the left Trackball button twice. The system will complete
the trace and display the result next to the trace.
NOTE: It is possible to perform measurements on images being viewed from the
Study List, but the measurements cannot be saved in this case.

Scanning
Adding Text Annotations to Studies

Text labels can be added and saved to images.
To add text annotations or a pointer to an image screen:
1. Press the Text Soft Key.
2. Use the controls described in the Text Annotation Functions table to add text labels.
3. To exit Text mode, press the Exit Text Soft Key. When you save an image with text
annotations, the text will be saved with the image.
NOTE: Text cannot be added to images displayed in View mode.
Text Functions
Text Annotation Functions

Text Function Description
New Creates a new text label.
Use the on-screen keyboard or an external keyboard to type the text and
add it to the list.
Exit Text Closes the Text menu.
Clear Clears all text labels on the current image.
Pointer Use the pointer to select a location for the text label. Provides an arrow
point to place in an area of interest.
Use the Trackball to position the pointer, then press the left Trackball
button to place it in the area of interest. The small (inner) Rotary knob may
be used to rotate the orientation of the arrow in Annotation mode.
Text List Provides a list of the text entries that have been created on the system.
These are presented in most recently used order. The small Rotary knob
highlights entries in the text list. When you have highlighted the desired
entry, press the left Trackball button to activate the term so it can be placed
in the image using the Trackball. You can also directly activate the entry by
clicking on it in the list using the Trackball.
Right Mouse Key Removes a highlighted entry from the text list.

Wireless Probes
6 Wireless Probes
This chapter contains information about operating the ACUSON Freestyle system with wireless
probes.
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-3
Antenna Locations. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-3
Equipment Setup for Optimal Scanning. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-4
Connecting a Wireless Probe. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-5
Problems Connecting. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-5
Wireless Signal Quality. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-6
Monitoring Wireless Signal Quality . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-7
Wireless Signal Quality Meter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-7
Number of Bars in the Wireless Signal. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-7
Average Noise Level Indicator. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-8
Wireless Noise Examples . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-10
B-Mode Wireless Noise. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-10
Reasons for a Low Wireless Signal in B-Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . 6-10
Color Flow Wireless Noise. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-10
Reasons for a Low Wireless Signal in Color Flow . . . . . . . . . . . . . . . . . . . . . . . . 6-10
Finding/Locating Wireless Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-11
Using Multiple Probes. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-12
More than One Wireless Probe . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-12
A Probe Connected via Adapter Cable. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-12
Powering Down the Probe . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-12

Wireless Probes

Wireless Probes
Overview
When the system is operated in “wireless mode” the probe Cable Adapter is not used;
instead, the probe and console communicate wirelessly. To obtain successful results scanning
wirelessly, follow the instructions provided here.
NOTE: Consult the Safety chapter and System Reference manual for important
information about wireless operation and electromagnetic compatibility issues
associated with the system.
NOTE: See the Safety chapter and System Reference manual for important
information about the ACUSON Freestyle wireless probe specifications,
electromagnetic compatibility considerations, and security features.
Antenna Locations
The probe antennas are located towards the back of the probe (the back is the part with the
probe controls). If possible, keep your hand away from this area for optimal operation.
Additional antennas are also located in the midsection of the probe.
The system antennas are located in the upper left corners of the console. Maintain an
unblocked line of sight between the probe and the console for optimal operation.
Location of Probe Antennas on Probe and Console
1. Probe antennas
2. Console antennas

Wireless Probes
Equipment Setup for Optimal Scanning

The radio frequency (RF) transmitters used in the ACUSON Freestyle to send image data from
the probe to the console are designed to cover distances of no more than three (3) meters. It is
important to make sure that the distance between the probe and the console does not exceed
three (3) meters. Improved performance may be achieved with shorter distances.
When scanning, do not hold your hand at the back of the probe because by doing so you
may cover up the primary internal antennas and disrupt the wireless communication with the
console. Hold your hand towards the front of the probe.
The console and the probe should be oriented with the console facing the location of the
transducer with a clear line of sight. The quality of the wireless link is weakened if the co-
location of the two is too far out of plane, horizontally or vertically. The antennas in the console
that communicate with the probe are located in the upper-left corner of the front of the display.
Do not block these console locations; they must form a clear line of sight with the probe.
NOTE: Noise on the image, or disruptions in the wireless link, may be caused by
RF generators in the vicinity. If problems occur, try relocating offending devices away
from the system.
CAUTION: Operating more than one ACUSON Freestyle system in wireless probe
mode in the same room where a probe is within five (5) meters of an unintended console
unit, may cause interference problems on the unintended console unit. If this occurs,
increase the distance from the probe to the unintended console unit until the interference
disappears.

Wireless Probes
Connecting a Wireless Probe

NOTE: For important information about the Wireless Signal Quality meter and
the Average Noise Level index which are displayed during wireless scanning, see
“Wireless Signal Quality” on page 6-6 in this chapter.
To connect a wireless probe to the system:

1. With the console unit powered on, hold the probe within three meters of the console, with
a line-of-sight to the front of the console, and without obstructions between the probe and
the console.
2. Turn the probe on by continuously pressing both circular buttons on the probe until you
hear a beep that indicates the probe is powered on. The probe sends a signal to the
console requesting the connection. The console displays this message: “Connecting to
Probe” with the unique probe ID number, and sends a return signal which establishes the
connection.
3. When the connection is made, the console screen displays this message: “Wireless
connection established.”
4. Next, the message “Configuring System” is displayed and the console will beep. The
console screen will show the probe battery symbol. You can now begin real-time
scanning.
This process normally takes under three seconds to complete.
Problems Connecting
If the probe and console cannot establish a connection within ten seconds, the process is
terminated and the probe is automatically powered off.
The console displays a status message: “Wireless connection timed out.”
This situation can occur due to improper probe/console positioning. Check your equipment
setup, then repeat the connection process by turning the probe back on again.
NOTE: For proper probe/console positioning, follow the instructions described in
“Equipment Setup for Optimal Scanning” on page 6-4.

Wireless Probes
Wireless Signal Quality

The Freestyle console has a wireless signal quality meter that represents the wireless probe
signal quality. Always position the probe and system to maximize the signal quality.
By staying inside the 3 meter range and maintaining a good line-of-sight between the probe
and the console — without obstructing the antennas — you will be able to operate with good
results.
PATIENT NAME
PATIENT ID XXX
L13-5
Nerve Gen XXX
2.5cm
G 9
CG 10
XXX
SC 3
SF 6 XXX
PP 10
55dB
CF 1 XXX
CP 1
Vel 1
Pri 4
XXX
20 Hz
XXX
XXX
ANL 0.0 dB
XXX XXX XXX XXX

P S
The Wireless Signal Quality Meter indicates the wireless probe link quality; best signal quality is six bars.
The number of bars on the wireless signal quality meter has been empirically correlated to the
potential for artifact to be introduced into the image because of a weak signal. This correlation
has been experimentally quantified for a variety of system settings, probe types, image
characteristics, and bit error levels in the wireless signal.
Use the display as a guide to maintaining a good link, following the guidelines below.

Wireless Probes
Monitoring Wireless Signal Quality

The Freestyle has two methods of monitoring wireless signals:
■■ Wireless Signal Quality meter
■■ Average Noise Level indicator
Each is described in the following sections.
Wireless Signal Quality Meter

The signal meter has a total of six bars.
No Signal
OK
P S
1 2 3 4 5
Wireless Signal Quality Meter; showing five different conditions
Number of Bars in the Wireless Signal

The number of bars in the wireless signal quality meter correlates to the potential of artifact
being introduced because of a weak signal.
Always monitor the number of bars displayed in the meter. See the following table for a
description of the conditions.
Wireless Signal Quality Meter Conditions

Number of Bars Condition Expectations
4 to 6 The best signal quality. Expect a very reliable wireless probe performance without
noise being introduced because of wireless link quality
3 Very reliable wireless probe performance, this noise is typically imperceptible, but
there is a possibility of low levels of noise (artifacts) being introduced into the image
because of a compromised wireless probe link.
Reorient the probe/console to within 3 meters of each other, in a line-of-sight,
without obstructions between the probe and the console.
2 or 1 There is an increased possibility of noise (artifacts) being introduced to the image
because of a compromised wireless probe link. These artifacts may appear as
bright, streaky lines. See the image in “B-Mode Wireless Noise” on page 6-10.
0 The wireless signal has been lost, so the image screen is blank. A message
appears on the console screen informing you of this condition.

Wireless Probes
Average Noise Level Indicator

An additional indicator of wireless imaging quality, called the Average Noise Level (ANL)
has been calculated for various conditions. ANL is another tool to guide wireless scanning. It
provides a measure of the potential for a compromised wireless link to introduce noise artifact
into the image. ANL is displayed in real-time above the wireless signal quality meter.
ANL is displayed in dB. An ANL value of 0.0 represents the optimal setting and indicates that
the signal quality is very good and free of errors that might introduce noise into the image.
Be alert to the ANL level, in accordance with the guidance below. To insure optimal wireless
imaging, use the information from both the wireless signal quality meter and the ANL.
PATIENT NAME
PATIENT ID XXX
--------
L13-5
Nerve Gen XXX
2.5cm
G 9
CG 10
XXX ANL 0.0 dB
SC 3
SF 6 XXX
PP 10 --------
55dB
CF 1 XXX
CP 1
Vel 1
Pri 4
XXX ANL 0.5 dB
20 Hz
XXX --------
XXX
ANL 0.0 dB
ANL 1.3 dB
--------
XXX XXX XXX XXX

P S
ANL 2.9 dB
--------
No Signal
OK
P S
--------
Five different Average Noise Level (ANL) conditions; last one showing “No Signal”

Wireless Probes
The wireless Average Noise Level (ANL) is displayed in real-time. Examples are provided
above. Values above the 0.0 level reflect an increased possibility of noise being introduced into
the image because of a compromised wireless link. The upper range is approximately 4.0 dB.
For best results position the probe and system such that ANL is not above 1.0 dB.
Always monitor the noise levels on the console. See the following table for a description of the
conditions.
Average Noise Level Indicator Conditions

ANL decibels (dB) Condition Expectations
0.0 to 0.3 Expect very reliable wireless probe performance without noise being
introduced because of wireless link quality.
0.4 to 1.0 Very reliable wireless probe performance, but there is a possibility of low
levels of noise being introduced into the image because of a compromised
wireless probe link. This noise is typically imperceptible.
Reorient the probe/console to within 3 meters of each other, in a line-of-
sight, without obstructions between the probe and the console.
Signal There is an increased possibility of noise being introduced to the image
less than 1.0 because of a compromised wireless probe link.
No signal The wireless signal has been lost, so the image screen is blank. A
message appears on the screen informing you of this condition and the
ANL display is also blank.

Wireless Probes
Wireless Noise Examples
B-Mode Wireless Noise

In B-Mode, if the wireless signal quality is compromised, noise may occur as shown in the
simulated image below. If you experience such noise, reposition to improve the link quality.
B-Mode wireless noise (simulated image)
Reasons for a Low Wireless Signal in B-Mode

■■ The probe is too far away from the console
■■ The probe is out of a line-of-sight to the console
■■ There is an obstruction between the probe antennas and the console antennas
■■ Some combination of these
Color Flow Wireless Noise

In Color Flow Doppler mode, if the wireless signal quality is compromised, excess background
noise, as demonstrated in the simulated phantom flow image here may occur. If you experience
such noise, reposition to improve the link quality.
Color Flow Doppler wireless noise (simulated image)
Reasons for a Low Wireless Signal in Color Flow

■■ The probe is too far away from the console
■■ The probe is out of a line-of-sight to the console
■■ There is an obstruction between the probe antennas and the console antennas
■■ Some combination of these

Wireless Probes
Finding/Locating Wireless Probes

It is very important to carefully manage the location of your wireless probes and not misplace
them. Do not leave probes behind when performing mobile procedures.
The system provides a means of assisting in preventing the unintentional separation of the
wireless probe from the console. This feature uses the Bluetooth radios in the probe and
console to provide a basic level of monitoring of the connection and proximity of the wireless
probe to the console.
1. Enable PROBE LOCALIZATION in the SETUP / SYSTEM / ADMIN page.
2. When Probe Localization is enabled the system will monitor the Bluetooth signal strength
between the probe and the console when:
–– the wireless probe is turned on and connected, and
–– there is a scanned image in Freeze mode on the console
If the signal falls below a threshold, it may mean that the separation distance is
greater than is normally used for scanning. It may also mean that the probe is being
unintentionally separated from the console. In this situation, the probe will beep, and
the system will display a message on the screen advising you to locate and secure the
identified probe.
3. Press OK or Silence to acknowledge this message.
With a probe turned on and connected wirelessly, you can also help locate a probe by selecting
SETUP / PROBES and pressing the IDENTIFY button. This will cause the connected probe to
beep.
With a probe turned on and connected wirelessly, when you turn the system console off, the
probe will beep.
NOTE: The localization feature requires a probe to be turned on and connected

wirelessly to the console, and to be in Freeze, that is, not live scanning. Enabling
Automatic Freeze in the SETUP / SYSTEM / ADMIN page will improve the
function of this feature by automatically freezing the system when imaging is
not active. This feature is subject to uncertainties inherent to Bluetooth radio
connection quality and should not be relied on as a primary means of locating
probes.

Wireless Probes
Using Multiple Probes

Multiple probes can be used with the system, but only one probe can be activated at a time.
More than One Wireless Probe

To use more than one probe in wireless mode during an exam:
1. Turn the currently-connected probe off, thereby disconnecting it from the console.
2. Position the second probe and turn it on.
A Probe Connected via Adapter Cable

If a Probe is connected to the console with the probe Adapter Cable, you will need to
disconnect it to make a wireless connection to another probe. Disconnect it at either the probe
or the console end.
Powering Down the Probe

When you have finished scanning with the connected probe and are ready to either clean it
or store it, power it down by continuously pressing both circular buttons on the probe until it
beeps.
When the probe is turned off, the battery symbol will disappear from the display. Removing the
battery also powers the probe down.
Before trying to scan with a new probe, be sure to power the active probe off.
NOTE: During the course of a procedure, it is recommended that you leave the
probe powered on so that the probe localization feature may function. See “Finding/
Locating Wireless Probes” on page 6-11 for more information.
NOTE: For important information about the ACUSON Freestyle wireless probe
specifications, electromagnetic compatibility considerations, and security features,
see the Safety and Warnings chapter.

Batteries
7 Batteries
This chapter contains information regarding the battery operation of the system and wireless
probes.
Overview of the Probe Battery. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-3

Charging the Probe Battery. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-4
Checking the Status of Charging Batteries . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-4
Inserting the Battery into the Probe. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-5
Monitoring the Battery Charge Level while Scanning . . . . . . . . . . . . . . . . . . . . . . . . . . 7-5
Low Battery Alerts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-6

Batteries

Batteries
Overview of the Probe Battery

WARNING: Read the Safety Chapter of this manual for important information regarding
safe operation of the ACUSON Freestyle batteries.
WARNING: To avoid the risk of electrical shock, do not insert the battery pack into probe
or charger bays unless the battery pack, probe, or charger bays are dry and free of
liquids.
CAUTION: Verify that the probe battery pack and either the probe battery receptacle or
the System charging bays are free of any liquid, gels, or contaminants before inserting
the battery. Inserting a battery into the probe or charger bays when liquid, gel, or
contaminants could cause harm to the probe and/or system.

1
2 3
The probe battery is recharged in the charging bays at the rear of the
System Console; when charged, return it to the probe
1. Probe charging bays

2. Probe battery
3. Probe

Batteries
Charging the Probe Battery

Successful wireless probe scanning without interruption requires a properly charged battery
pack. To charge the probe batteries, use the on-board two-port charging bays built into the
back of the console.
For optimal charging in the console charging ports, the console should be plugged into AC
Mains power outlet. If the system is unplugged from the AC mains power outlet, the probe
batteries will recharge from the batteries inside the console, provided that those batteries have
sufficient charge to do so. If the console internal batteries are depleted, and the console is
unplugged, the probe batteries will not recharge.
To charge the probe battery, follow these steps:
1. Remove the probe battery from the probe by placing a finger at the back of the pack in
the indentation and applying forward and outward pressure on the latch. As the battery
releases from its compartment, be sure to prevent it from falling to the floor.
2. Place the battery into one of the console’s charging bays with the metal contacts facing
inwards. To be sure that the pack is properly engaged, confirm that the light next to the
bay is lit, but not flashing.
NOTE: The probe’s battery pack is “keyed” to prevent improper insertion.
CAUTION: The battery pack is keyed to fit into the charging bay in the proper orientation.
Do not use excessive force in inserting the pack into the charging bay. Make sure that you
have lined it up properly when inserting.
3. Confirm the status of the probe batteries in the charging bays by checking the Battery
page in the SETUP Menu. Even if the console has enough battery charge to charge the
probe batteries, if the console battery charge is low, you should plug it into an AC Mains
power outlet.
Checking the Status of Charging Batteries

Charging status can be checked in two places: the charging bay and the console screen.
When the probe batteries are properly placed in the charging bay, a small light next to each
bay will light to show the status of that battery.
■■ A green light means the battery is fully charged.
■■ A steady amber light means the battery is charging.
When probe batteries are being charged in the console charging bays and the system is on,
their charging status is displayed at the top of the system screen directly under the probe
battery.
Five dashed lines represent the charge status, with the bright dashes representing the battery
charge level. For example, four bright dashes and one dim dash mean the battery is at least
80% charged. Charge status is also displayed in the SETUP / SYSTEM page.

Batteries
Inserting the Battery into the Probe

To insert a charged battery pack into a probe:
1. Place the metal contact side facing into the well on the probe with the label facing down
and the metal contacts towards the back of the probe.
CAUTION: The battery pack is keyed to fit into the probe in the proper orientation. Do not
use excessive force in inserting the pack into the probe. Make sure that you have lined it
up properly when inserting.
CAUTION: Use only your fingers to insert and remove the battery pack from either the
probe or the charging ports. Do not use tools. Use of tools may damage the battery pack
Monitoring the Battery Charge Level while Scanning

During live scanning, monitor the charge level status of the probe battery by observing the
probe battery (“P”) symbol and the system console battery (“S”) on the screen.
The green portion of the battery symbol represents the estimated charge remaining. Typically,
a fully-charged probe battery will provide approximately one hour of scanning.
NOTE: The estimated charge remaining is an approximation, and numerous factors,
such as scanning mode and battery age can affect its accuracy.
When the probe battery charge level goes below 20%, the light on the probe changes to
amber.
P S S
On-screen display of the Probe battery charge level (shown partially charged), System battery charge level (shown
fully charged), and the System power plug symbol (when the system console is plugged into an AC Mains power outlet
instead of running on battery power)

Batteries
Low Battery Alerts

A pop-up message on the console will alert you when the probe battery approaches
approximately 20% of remaining power.
You should then take action to avoid an interruption to the exam:
1. Freeze the image.
2. Turn the probe off.
3. Replace the probe battery with a fresh battery.
4. Turn the probe on and resume the exam.
Alternatively, you can begin using the probe cable connector or proceed to promptly complete
the exam.
When the system battery approaches 10% the battery alert message will be repeated. Shortly,
following that, the probe will automatically shut down. When the 10% remaining charge
message appears, you should take action so as not to interrupt the exam.
When the system is plugged into AC Mains power, if the console batteries require recharging,
and probe batteries are inserted into the onboard charging ports and also require recharging,
the system will give higher priority to recharging the probe batteries.

Connectivity
8 Connectivity
This chapter tells you how to configure your system for connectivity, and how to operate
connectivity commands.
Overview of Connectivity. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-3

Configuring the Network Settings. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-3
Ethernet Setup. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-3
Wireless Network Setup. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-4
Working with Multiple WiFi Networks. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-4
Detecting WiFi Networks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-4
Configuring the WiFi Network. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-5
Configuring the DICOM Setup. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-6
DICOM Setup Menu Soft Keys. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-6
Configuring a DICOM Storage Server. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-7
Configuring a DICOM Storage Commitment Server . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-8
Configuring a Modality Worklist Server . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-9
Configuring the System DICOM Settings. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-10
Freestyle Mobile Link App . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-11
Freestyle Mobile Link Settings. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-11
Privacy and Security . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-12

Connectivity

Connectivity
Overview of Connectivity
The ACUSON Freestyle includes the DICOM (Digital Imaging and Communications in Medicine)
networking capability. DICOM communications comply with the DICOM standard and provide
links between the system and DICOM picture archival systems (PACS), modality worklist
servers, and storage commitment servers.
Consult with your PACS Administrator when using the DICOM features of the ACUSON
Freestyle.
NOTE: Confirm compatibility between your DICOM PACS system and the ACUSON
Freestyle before archiving from the ACUSON Freestyle to the PACS system.
System configuration for connectivity are usually carried out by your organization’s network or
PACS Administrators.
Connectivity features may be options which are not provided on every system.
Configuring the Network Settings

To configure your system for connectivity, go to SETUP / SETTINGS / NETWORK. This takes you
to the Network page.
Ethernet Setup
This defines the network identification of the system, using the IP address, Subnet Mask and
Gateway to give the ACUSON Freestyle a unique identifier on a specific network.
Check the Auto IP Enabled box to enable the IP address to be assigned on startup.
Ethernet Network Configuration Fields

Network Field Description
IP Address When checked allows the system to automatically obtain an IP
Address.
Auto IP Enabled Automated IP address assignment.
Subnet Mask IP address formatting.
Gateway Network access point.
[OK] Saves the settings for the network.
[Cancel] Closes the menu without saving settings.
To edit the IP Address, Subnet Mask, or Gateway, click on the typewriter symbol next to the
field.
NOTE: The MAC address displayed cannot be edited.

Connectivity
Wireless Network Setup

NOTE: The term “WiFi” is used here to represent the wireless networking standard
IEEE 802.11b/g. Refer to the Safety chapter of this Manual and the System
Reference Manual for important information about the operation of IEEE 802.11b/g
on the ACUSON Freestyle.
Important: For important information about WiFi Security, refer to the System Reference
Manual.
Use the WiFi Setup section of the Network page to configuring the ACUSON Freestyle to
connect to a wireless network (go to SETUP / SETTINGS / NETWORK).
To turn wireless networking on and off, use the Enable WiFi checkbox. When wireless
networking is enabled, the system will automatically search for and connect to configured
wireless networks in range, according to their order in the list.
NOTE: Follow your institution’s guidelines for wireless networking security, and
consult with your IT administrator when configuring the system for WiFi connectivity.
Even secured WiFi networks may be the subject of unauthorized access.
The system can be configured to store multiple wireless network configurations.
Working with Multiple WiFi Networks

If multiple WiFi networks have been set up, use the options described in “Configuring the WiFi
Network” on page 8-5 to manage them.
■■ Move Up: moves a network up in the list.
■■ Move Down: moves a network down in the list.
■■ Release: disconnects a connected WiFi network.
■■ Connect: manually connects to the selected WiFi network.
■■ Edit: modify the settings for a WiFi network.
■■ Add: initiates a search for wireless networks.
■■ Remove: deletes a network from the list.
Detecting WiFi Networks

Use the following options to detect WiFi networks:
■■ To detect and display WiFi networks, select Add.
■■ To repeat the search, select Refresh Network List.
■■ To manually enter a WiFi network settings, select Manual Entry.
■■ To open the WiFi Network Settings menu, double-click on a detected WiFi network. Use
this option to configure the network.

Connectivity
Configuring the WiFi Network
WiFi Network Configuration Fields

Network Field Description
Network Name Unique name to identify the network in the Network List.
Network Type Select either Infrastructure or Adhoc.
• Infrastructure uses central access points such as routers for
communication.
• Adhoc allows wireless devices to communicate in a peer-to-
peer fashion.
Security Use the drop-down menu to select the security method used
by the WiFi network. See the Safety chapter of this Manual for
information about 802.11 b/g security.
Use the data entry fields in the security box to enter security
data. To import Enterprise WiFi Certificate data, select IMPORT
CERTIFICATE. Copy the certificate to a USB drive, then plug the
USB drive into the Freestyle. Select the certificate file name and
press OK to import the certificate.
IP Address When checked allows the system to automatically obtain an IP
Address.
[OK] Saves the settings for the network.
[Cancel] Closes the menu without saving settings.

Connectivity
Configuring the DICOM Setup

To access the DICOM setup menus, select SETUP / SETTINGS / DICOM.
DICOM Configuration Fields

DICOM Field Description
PACS Configures the ACUSON Freestyle to link to a DICOM-compliant
Picture Archival and Communications System (PACS).
Storage Commitment When on, supported by your PACS system and, configured on
the ultrasound system, confirms that a study has been received
and stored by the target device.
Worklist When supported by your PACS system and configured on
the ultrasound system, manages the ACUSON Freestyle’s
communication with a DICOM Worklist Server to download
patient information.
System Sets the DICOM AE Title (the name the system provides to the
DICOM server) and the port to use.
DICOM Setup Menu Soft Keys

In the DICOM setup menus, the Soft Key functions include:
NEW– to add a new network connection.
DELETE – deletes a selected network connection.
EDIT – to edit or configure a network connection.
EDIT OK – confirms the values that were entered.

Connectivity
Configuring a DICOM Storage Server

To configure a DICOM storage server,
1. Go to SETUP / SETTINGS / DICOM / PACS.
2. Select New.
3. Enter the DICOM storage server information as described in the following table.
DICOM Storage Server Fields

DICOM Storage Server Description
Field
Alias A name you create to identify the DICOM server.
Limited to 16 characters.
IP Address The IP (Internet Protocol) address for the server. See your System
Administrator to determine your IP Address.
AE Title Identifies the server application that receives the images from the
ACUSON Freestyle. The alphanumeric characters entered in this
field must exactly match (including case) the Application Entity name
assigned to the server application.
Limited to 16 characters; cannot include the period (“.”) character.
Port Number The remote port on the server that is to receive the connection
request and the patient studies.
The default setting is 104.
Test Used to test the connection once you have entered the configuration
data. You can test using either Ping or C-Echo (DICOM Verify). Ping
tests the connection across the network; C-Echo additionally tests
that the DICOM server is active.
For security reasons, some network and network servers are set up
not to respond to Ping or C-Echo commands. Check with your IT
department or PACS Administrator to determine how your network
handles these functions.

Connectivity
Configuring a DICOM Storage Commitment Server

To configure a DICOM Storage Commitment Server:
1. Go to SETUP / SETTINGS / DICOM / STORAGE COMMITMENT.
2. Select NEW.
3. Enter the DICOM Storage Commitment information as described in the following table.
DICOM Storage Commitment Fields

Field Description
Alias Name you define for the Storage Commitment Server.
IP Address The IP address of the Storage Commitment Server.
AE Title Identifies the server application that receives storage commitment
messages from the ACUSON Freestyle. The alphanumeric characters
entered in this field must exactly match (including case) the Application
Entity name assigned to the server application.
Port Number The remote port on the server that is to receive the storage
commitment messages.
The default is port 104.
tests the connection across the network; C-Echo additionally tests that
the DICOM server is active.
NOTE: If you enable Storage Commitment but your DICOM server does not support
this feature, the system will not perform the Storage Commitment function.
It can take several minutes for the Storage Commitment Server to respond to a storage
commitment request. During that time, any other transfers that have been lined up will
continue.

Connectivity
Configuring a Modality Worklist Server

To configure a DICOM Modality Worklist Server:
1. Go to SETUP / SETTINGS / DICOM / WORKLIST.
2. Select NEW.
3. Enter the DICOM Worklist information as described in the following table.
DICOM Worklist Fields

Field Description
Alias Name you define for the server.
IP Address The IP address of the Server.
AE Title Identifies the server application that receives worklist messages from
the ACUSON Freestyle. The alphanumeric characters entered in this
field must exactly match (including case) the Application Entity name
assigned to the server application.
Port Number The remote port on the server that is to receive the worklist messages.
The default is port 104.
tests the connection across the network; C-Echo additionally tests that
the DICOM server is active.
NOTE: If you enable Worklist but your DICOM server does not support this feature,
the system will not perform the Worklist function.

Connectivity
Configuring the System DICOM Settings

To configure the ACUSON Freestyle System DICOM settings:
1. Go to SETUP / SETTINGS / DICOM / SYSTEM.
2. Enter the system information as described in the following table.
DICOM System Settings Fields

Field Description
Freestyle AE Title Identifies the AE Title assigned to the system.
Freestyle Port The port on the system used for DICOM messages.
Number The default is port 104.

Connectivity
Freestyle Mobile Link App
NOTE: Images displayed using the App are for informational purposes only and are
not intended for diagnostic use.
For instructions on using the Mobile Link App on a mobile device, see the instructions provided
with the App.
Freestyle Mobile Link Settings
Freestyle Mobile Link App Settings

Function Instructions Additional Information
Enable Mobile Link Select: SETUP / SYSTEM / ADMIN. The App links using the WiFi connection.
Check the Enable Mobile App checkbox. When the Mobile Link App is Enabled, the
mobile symbol appears on the console
imaging screen:
To disable the Mobile Link, uncheck the box.

Set Security Note that the PIN code specified here must
PIN Code also be entered on the Windows mobile
device in order to link to the Freestyle.
Select: SETUP / SETTINGS / NETWORK.
Go to the Mobile Link section.
Select: PIN Code.
Enter a four-digit PIN Code. After entry, the PIN code is not displayed.
Confirm Port The port number entered for the Freestyle If the port number is changed, the Freestyle
Number must be the same as the number entered in must be restarted.
the App.
Activate New Patient After sending patient study information from —
Study from App the App, select NEW PATIENT / WORKLIST.
Highlight the patient entry and select Create
Study.

Connectivity
Privacy and Security

To insure proper protection of Protected Health Information and networking security when using
the App, note the following recommendations and instructions.
■■ For important information about 802.11 (WiFi), refer to the Freestyle User Manual and
System Reference Manual.
■■ For important information about Protected Health Information (patient privacy), refer to the
Freestyle User Manual and System Reference Manual.
■■ Follow your regional and institutional guidelines regarding networking security and
Protected Health Information (patient privacy).
■■ If you do not want mobile devices to link to the Freestyle using the Mobile Link App,
uncheck (disable) the box on the SETUP / SYSTEM / ADMIN page.
■■ If a mobile device is connected through the Mobile Link App, the mobile symbol ( ) will
be displayed on the console screen.
■■ Protect the security of the PIN code used to allow devices to link. Change the PIN code if
necessary to improve security.
■■ To prevent the patient name and ID from being displayed on saved images, use the Study
Anonymity feature. Select SETUP / SYSTEM and check the two checkboxes to exclude
Patient Name and Patient ID. Note that the Patient Name will still show up in the patient
list.
■■ To create a fully anonymous study file, follow these steps: create a new patient study but
do not enter a patient name of ID. When you select Save, to save the images, the system
will automatically assign the name “UNKNOWN” and a date- and time-based ID.

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ACUSON Freestyle

Diagnostic Ultrasound System

Siemens Medical Solutions USA, Inc. 11002778_01 English

Asepti-Wipe, Cidex, Gigasept, MetriCide, T-Spray, EU Authorized Representative

Chapter 2 Safety and Care

Chapter 3 System Setup

Chapter 4 Patient Studies

Chapter 6 Wireless Probe Operation

ACUSON Freestyle User Manual iii

iv ACUSON Freestyle User Manual

About the User and Reference Manuals

ACUSON Freestyle User Manual v

Warnings, Cautions, and

CAUTION: Cautions are intended to alert you to the

vi ACUSON Freestyle User Manual

ACUSON Freestyle User Manual vii

2 Safety and Care

viii ACUSON Freestyle User Manual

Electrical Safety. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-17

ACUSON Freestyle User Manual ix

Disposing of the Packaging Materials. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-46

x ACUSON Freestyle User Manual

Probe Shortcuts for Save and Color. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-4

ACUSON Freestyle User Manual xi

xii ACUSON Freestyle User Manual

System Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3

ACUSON Freestyle User Manual 1-1

1-2 ACUSON Freestyle User Manual

Console Front View

XXX XXX XXX XXX

System Console: Front View

ACUSON Freestyle User Manual 1-3

Console Rear View

System Console: Rear View

1-4 ACUSON Freestyle User Manual

Console Inputs/Outputs Panel

Inputs/Outputs Panel along right side of system console

1. Probe Adapter Cable connector

ACUSON Freestyle User Manual 1-5

Turning the System On and Off

Location of Console Power Key

Turn the System On

1-6 ACUSON Freestyle User Manual

Turn the System Off

ACUSON Freestyle User Manual 1-7

Imaging Screen Layout

Sample Imaging Screen

Sample ACUSON Freestyle Console Screen

1-8 ACUSON Freestyle User Manual

2 Safety and Care

Operating Safety and Environment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-3

ACUSON Freestyle User Manual 2-1

Cleaning and Disinfecting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-27

2-2 ACUSON Freestyle User Manual

Operating Safety and Environment

Consult instructions for use

Consult instructions for use

Ethernet 10/100BaseT/1000BaseT Connection

Type B Applied Part