GE Venue 50 User Manual

Technical Publications
Direction 5446729-100 English

Rev. 7
Venue 50 Basic User Manual
R4.x.x
Operating Documentation
Copyright 2013-2014 By General Electric Co.
Regulatory Requirement
Venue 50 complies with regulatory requirements of the following European

Directive 93/42/EEC concerning medical devices.
This manual is a reference for the Venue 50. It applies to all versions of the R4.x.x
software for the Venue 50 ultrasound system.
GE
P.O. Box 414, Milwaukee, Wisconsin 53201 U.S.A.
(Asia, Pacific, Latin America, North America)
GE Ultraschall Deutschland GmbH & Co. KG

Beethovenstrasse 239
Postfach 11 05 60
D-42655 Solingen GERMANY
TEL: 49 212.28.02.208; FAX: 49 212.28.02.431
Revision History
Reason for Change
DATE
REV (YYYY/MM/DD) REASON FOR CHANGE
Rev.1 2013/01/04 Initial Release
Rev.2 2013/05/21 Update UI and software functions
Rev.5 2014/01/13 Update UI
Rev.6 2014/03/13 Remove “NOTE: 10C-SC is not available in U.S.”
Rev.7 2014/09/05 Software updated
List of Effective Pages
REVISION REVISION
SECTION NUMBER NUMBER SECTION NUMBER NUMBER
Title Page Rev. 7 Chapter 3 Rev. 7
Revision History Rev. 7 Chapter 4 Rev. 7
Regulatory Requirements Rev. 7 Chapter 5 Rev. 7
Table of Contents Rev. 7 Chapter 6 Rev. 7
Chapter 1 Rev. 7 Index Rev. 7
Chapter 2 Rev. 7
Please verify that you are using the latest revision of this document. Information
pertaining to this document is maintained on MyWorkshop (GE electronic Product Data
Management). If you need to know the latest revision, contact your distributor, local GE
Sales Representative or in the USA call the GE Ultrasound Clinical Answer Center at
1 800 682 5327 or 1 262 524 5698.
Venue 50 – Basic User Manual i-1

Direction 5446729-100 English Rev. 7
This page intentionally left blank.
i-2 Venue 50 – Basic User Manual

Regulatory Requirements
Conformance Standards
The following classifications are in accordance with the IEC/
EN 60601-1:
• According to 93/42/EEC Medical Device Directive, this is
Class IIa Medical Device.
• According to IEC/EN 60601-1,
• Equipment is Class I, Type B with BF Applied Parts.
• Docking Station/Cart is Class 1.
• Continuous Operation.
• According to CISPR 11,
• Equipment is Group 1, Class A ISM Equipment.
• Docking Station/Cart is Group 1, Class A ISM
Equipment.
• According to IEC 60529,
• The footswitch rate is IP X8 (MKF 2 1S/1S-MED HID
GP 26).
• Probe head (immersible portion) and cable are IPX7.
Probe connector is not waterproof.
This product complies with the regulatory requirement of the
following:
• Council Directive 93/42/EEC concerning medical devices:
the CE label affixed to the product testifies compliance to
the Directive.
The location of the CE marking is shown in the Safety
chapter of this manual.
Authorized EU Representative
European registered place of business:
GE Medical Systems Information Technologies GmbH
(GEMS IT GmbH)
Munzinger Strasse 5, D-79111 Freiburg, GERMANY
Tel: +49 761 45 43 -0; Fax: +49 761 45 43 -233

Conformance Standards (continued)
• International Electrotechnical Commission (IEC):
• IEC/EN 60601-1 Medical Electrical Equipment, Part 1
General Requirements for Safety.
• IEC/EN 60601-1-2 Electromagnetic compatibility -
Requirements and tests.
• IEC/EN 60601-1-6 (Usability), EN 1041 (Information
supplied with medical devices).
• IEC 60601-2-37 Medical electrical equipment. Particular
requirements for the safety of ultrasonic medical
diagnostic and monitoring equipment.
• International Organization of Standards (ISO):
• ISO 10993-1 Biological evaluation of medical devices.
• Canadian Standards Association (CSA):
• CSA 22.2, 601.1 Medical Electrical Equipment, Part 1
General Requirements for Safety.
• ANSI/AAMI ES60601-1.
• NEMA/AIUM Acoustic Output Display Standard (NEMA
UD-3, 2004).
• Medical Device Good Manufacturing Practice Manual
issued by the FDA (Food and Drug Administration,
Department of Health, USA).

Certifications
• General Electric Medical Systems is ISO 9001 and
ISO 13485 certified.
Original Documentation
• The original document was written in English.
Country Specific Approval

• JAPAN
MHLW Certified Number: 221ABBZX00092000
Importer Information
• Turkey

Table of Contents
Conformance Standards - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-3

Certifications - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-5
Original Documentation - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-5
Country Specific Approval - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-5
Importer Information - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-5
Table of Contents
Chapter 1 — Introduction/Safety
System Overview
Attention - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-2
Documentation - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-3
Principles of Operation - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-4
Indications for Use - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-5
Frequency of Use - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-5
Operator Profile - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-5
Prescription Device - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-5
Owner Responsibility
Owner requirements - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-6
Notice against user modification- - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-7
Safety Precautions
Precaution Levels - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-8
Hazard Symbols - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-9
Patient Safety- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-11
Equipment and Personnel Safety - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-15
General Caution - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-20
EMC (Electromagnetic Compatibility) - - - - - - - - - - - - - - - - - - - - - - - - 1-21
Patient Environmental Devices- - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-28
Acoustic Output - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-30
Device Labels
Icon Description - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-33
Warning label locations - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-37
Chapter 2 — Preparing the System for Use
Site Requirements
Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-2
Before the system arrives - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-3
Environmental Requirements - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-4
Acclimation Time - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-4
Console Overview
Console graphics - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-5
Peripheral/Accessory Connection- - - - - - - - - - - - - - - - - - - - - - - - - - - 2-13

System Positioning/Transporting
Moving the System - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-21
When moving the system - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-22
Transporting the System - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-24
Attaching the Security Cable - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-25
Powering the System
Connecting and Using the System - - - - - - - - - - - - - - - - - - - - - - - - - - 2-27
Adjusting the Display Monitor
Tilt LCD monitor - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-32
Adjusting the Docking Cart - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-33
Brightness - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-35
Probes
Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-36
Selecting probes- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-36
Connecting the Probe - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-37
Cable Handling - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-38
Deactivating the Probe - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-38
Disconnecting the Probe - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-39
Transporting Probes - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-40
Storing the Probe - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-40
Touch Panel
Exam Function Controls - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-41
Monitor Display
Monitor Display- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-42
Chapter 3 — Performing an Exam
Performing an Exam
Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-2
Begin a new exam
Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-3
Image Scanning
B Mode - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-8
Color Flow Mode - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-11
Power Doppler Imaging (PDI) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-14
M Mode - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-16
Measurements
Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-18
B Mode Measurements - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-19
M Mode Measurements- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-27
Obstetrics Measurements - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-31
Gestational Sac (GS) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-32
Crown Rump Length (CRL) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-34
Biparietal Diameter (BPD) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-35
Abdominal Circumference (AC) - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-36
Femur Length (FL) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-38
Antero-Postero Trunk Diameter by Transverse Trunk Diameter (AxT) - 3-39
Spine Length (SL)- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-40
Cardio-Thoracic Area Ratio (CTAR) - - - - - - - - - - - - - - - - - - - - - - - - - 3-41

Amniotic Fluid Index (AFI) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-42
Cervical Length (CL) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-44
Humerus Length (HL) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-45
Head Circumference (HC) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-46
Fetal Trunk Cross-Sectional Area (FTA) - - - - - - - - - - - - - - - - - - - - - - 3-48
Estimated Fetal Weight (EFW) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-49
Annotations
Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-50
Comment Retention - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-50
Annotating an image using the library - - - - - - - - - - - - - - - - - - - - - - - 3-51
Annotating an image with typed words - - - - - - - - - - - - - - - - - - - - - - - 3-55
Bodymark - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-56
Arrow Pointers - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-57
Edit while annotating - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-58
Annotation Controls - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-58
OB Worksheet
Activating the Worksheet - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-60
OB Worksheet Controls- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-61
OB Worksheet information- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-62
Editing OB Worksheet - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-70
OB Report - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-71
Multi gestational - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-73
Storing an OB Report - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-74
Image Management
Zooming an Image - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-75
Split Screen - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-76
Using Cine - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-77
Review Archived Information - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-80
Image Storage - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-88
eSmart Trainer (Option)- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-101
Chapter 4 — Customizing Your System
Utility
Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-2
General - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-3
Settings - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-5
Image - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-13
Measure - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-19
System - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-22
Connectivity - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-24
About- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-33

Chapter 5 — Probes and Biopsy
Probe Overview
Ergonomics - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-2
Cable handling - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-2
Probe orientation - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-3
Labeling- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-4
Probe Naming Conventions - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-4
Probe Usage - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-5
Care and Maintenance - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-5
Probe Safety - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-6
Special handling instructions - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-8
Probe handling and infection control - - - - - - - - - - - - - - - - - - - - - - - - - 5-10
Probe Cleaning Process - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-11
Probe Discussion
Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-19
Probe Applications - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-20
Probe Specifications - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-21
Probe Slice Thickness Specifications - - - - - - - - - - - - - - - - - - - - - - - - 5-21
Probe Illustration- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-22
Biopsy Special Concerns
Precautions Concerning the Use of Biopsy Procedures - - - - - - - - - - - 5-23
Preparing for a Biopsy
Displaying the Guidezone - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-25
Preparing the Biopsy Guide Attachment - - - - - - - - - - - - - - - - - - - - - - 5-28
Biopsy Needle Path Verification - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-38
The Biopsy Procedure- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-39
Post Biopsy - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-41
Surgery/Intra-operative Use
Preparing for Surgery/Intra-operative Procedures - - - - - - - - - - - - - - - 5-42
Chapter 6 — User Maintenance
System Data
Features/Specifications - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-2
Clinical Measurement Accuracy - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-8
Anti-Virus Software Note
Venue 50 Security - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-11
System Care and Maintenance
Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-13
Inspecting the System - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-14
Weekly Maintenance- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-15
Cleaning the system - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-16
Other Maintenance - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-19

Quality Assurance
Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-20
Typical Tests to Perform - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-21
Baselines - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-23
Periodic Checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-23
Results - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-24
System Setup- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-25
Test Procedures - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-25
Setting up a Record Keeping System - - - - - - - - - - - - - - - - - - - - - - - - 6-34
Ultrasound Quality Assurance Checklist - - - - - - - - - - - - - - - - - - - - - - 6-35
Supplies/Accessories
Peripherals- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-36
Console - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-37
Probes- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-37
Gel - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-37
Contact Information
Contacting GE Ultrasound - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-38
Manufacturer - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-44
Index

Chapter 1
Introduction/Safety
This chapter consists of information concerning

indications for use, how documents are organized (?),
and the safety and regulatory information pertinent for
operating this ultrasound system.
Venue 50 – Basic User Manual 1-1

Introduction/Safety
System Overview
Attention
This manual contains necessary and sufficient information to
operate the system safely.
Read and understand all instructions in this manual before
attempting to use the Venue 50 system.
Keep this manual with the equipment at all times. Periodically
review the procedures for operation and safety precautions.
Disregarding information on safety is considered abnormal use.
Not all features or products described in this document may be
available or cleared for sale in all markets. Please contact your
local GE Ultrasound representative to get the latest information.
NOTE: Please note that orders are based on the individually agreed
upon specifications and may not contain all features listed in this
manual.
NOTE: All references to standards/regulations and their revisions are
valid at the time of publication of the user manual.
1-2 Venue 50 – Basic User Manual

System Overview
Documentation
CAUTION Safety instructions must be reviewed before operating the unit.
Venue 50 documentation consists of various manuals:

• The Basic User Manual (TRANSLATED) and User Guide
(ENGLISH ONLY) provide information needed by the
operator to operate the system safely. They describe the
basic functions of the system, safety features, operating
modes, measurements/calculations, probes, user care and
maintenance.
• The Quick Card (TRANSLATED) provides descriptions of
basic system features and operation. It is intended to be
used in conjunction with the Basic User Manual in order to
provide the information necessary to operate the system
safely.
• The Release Notes (TRANSLATED) provide precautions
and instructions that supplement the Basic User Manual.
• The Advanced Reference Manual (ENGLISH ONLY)
contains data tables, such as Obstetrics (OB) and Acoustic
Output tables.
• The Service Manual (ENGLISH ONLY) supplies block
diagrams, lists of spare parts, descriptions, adjustment
instructions or similar information which helps qualified
technical personnel in repairing those parts of the system
which have been defined as repairable.
• AIUM Booklet (USA only)
The Venue 50 manuals are written for operators who are familiar
with basic ultrasound principles and techniques. They do not
include sonographic training or detailed clinical procedures.
NOTE: The screen graphics in this manual are only for illustrational
purposes. Actual screen output may differ.
NOTE: Probe information displayed on screen examples does not
necessarily reflect the probes available on your ultrasound
system. Please refer to the Probes chapter for a listing of
available probes and features.

Introduction/Safety
Principles of Operation
Medical ultrasound images are created by computer and digital
memory from the transmission and reception of mechanical
high-frequency waves applied through a transducer. The
mechanical ultrasound waves spread through the body,
producing an echo where density changes occur. For example,
in the case of human tissue, an echo is created where a signal
passes from an adipose tissue (fat) region to a muscular tissue
region. The echoes return to the transducer where they are
converted back into electrical signals.
These echo signals are highly amplified and processed by
several analog and digital circuits having filters with many
frequency and time response options, transforming the
high-frequency electrical signals into a series of digital image
signals which are stored in memory. Once in memory, the image
can be displayed in real-time on the image monitor. All signal
transmission, reception and processing characteristics are
controlled by the main computer. By selection from the system
control panel, the operator can alter the characteristics and
features of the system, allowing a wide range of uses, from
obstetrics to peripheral vascular examinations.
Transducers are accurate, solid-state devices, providing multiple
image formats. The digital design and use of solid-state
components provides highly stable and consistent imaging
performance with minimal required maintenance. Sophisticated
design with computer control offers a system with extensive
features and functions which is user-friendly and easy to use.

System Overview
Indications for Use

The Venue 50 is intended for use by a qualified physician or
sonographer for ultrasound evaluation.
The Venue 50 is intended for ultrasound imaging, measurement
and analysis of the human body for multiple clinical applications
including: Ophthalmic; Fetal/OB; Abdominal (GYN & Urology);
Pediatric; Small Organ (breast, testes, thyroid); Neonatal
Cephalic; Adult Cephalic; Cardiac (adult & pediatric); Peripheral
Vascular; Musculoskeletal Conventional & Superficial;
Transvaginal; Intraoperative (abdominal, thoracic and
peripheral); Thoracic/Pleural for motion and fluid detection and
imaging guidance of interventional procedures (Tissue Biopsy/
Fluid Drainage, Vascular Access, Nonvascular).
NOTE: Ophthalmic and Orbits are not available for Japan.
WARNING To avoid injury to the patient, select the Ophthalmic or Orbits

preset when performing an eye exam. The system will not
exceed the lower acoustic energy limits for ophthalmic use only
if the Ophthalmic or Orbits preset is selected.
Be sure to use the appropriate probes for eye scanning.
CAUTION This machine should be used in compliance with law. Some

jurisdictions restrict certain uses, such as gender
determination.
Frequency of Use
Daily (Typically 8 hours)
Operator Profile
• Qualified and trained physicians or sonographers with at
least basic ultrasound knowledge.
• The operator must have read and understood the user
manual.
Prescription Device
CAUTION: United States law restricts this device to sale or use
by, or on the order of a physician.

Introduction/Safety
Owner requirements
It is the responsibility of the owner to ensure that anyone
operating the system reads and understands this section of the
manual. However, there is no representation that the act of
reading this manual renders the reader qualified to operate,
inspect, test, align, calibrate, troubleshoot, repair or modify the
system. The owner should make certain that only properly
trained, fully-qualified service personnel undertake the
installation, maintenance, troubleshooting, calibration and repair
of the equipment.
The owner of the ultrasound unit should ensure that only
properly trained, fully qualified personnel are authorized to
operate the system. Before authorizing anyone to operate the
system, it should be verified that the person has read, and fully
understands the operating instructions contained in this manual.
It is advisable to maintain a list of authorized operators.
Should the system fail to operate correctly, or if the unit does not
respond to the commands described in this manual, the
operator should contact the nearest field GE Ultrasound Service
Office.
For information about specific requirements and regulations
applicable to the use of electronic medical equipment, consult
the local, state and federal agencies.
CAUTION For USA only:

Federal law restricts this device to use by, or on the orders of, a
physician.

Notice against user modification

Never modify this product, including system components,
software, cables, and so on. User modification may cause safety
hazards and degradation in system performance. All
modification must be done by a GE qualified person.

Introduction/Safety
Safety Precautions
Precaution Levels
Icon description
Various levels of safety precautions may be found on the

equipment and different levels of concern are identified by one
of the following flag words and icons which precede the
precautionary statement.
DANGER Indicates that a specific hazard is known to exist which through

inappropriate conditions or actions will cause:
• Severe or fatal personal injury
• Substantial property damage
WARNING Indicates that a specific hazard is known to exist which through

inappropriate conditions or actions may cause:
• Severe personal injury
• Substantial property damage
CAUTION Indicates that a potential hazard may exist which through

inappropriate conditions or actions will or can cause:
• Minor injury
• Property damage
NOTE: Indicates precautions or recommendations that should be used

in the operation of the ultrasound system, specifically:
• Maintaining an optimum system environment
• Using this manual
• Notes to emphasize or clarify a point

Safety Precautions
Hazard Symbols
Icon Description
Potential hazards are indicated by the following icons:
Table 1-1: Potential Hazards
Icon Potential Hazard Usage Source
Biological Hazard • Cleaning and care ISO 7000

Describes precautions necessary to instructions No. 0659
prevent the risk of disease transmission • Sheath and glove
or infection. guidelines
• Patient/operator infection due to
contaminated equipment
Electrical Hazard • Probes

Describes precautions necessary to • ECG, if applicable
prevent the risk of injury through electric • Connections to back
hazards. panel
• Electrical micro-shock to patient, e.g.,
ventricular
Moving Hazard • Moving

Describes precautions necessary to • Using brakes
prevent the risk of injury through moving • Transporting
or tipping hazard.
• Console, accessories or optional
storage devices that can fall on patient,
operator, or others
• Collision with persons or objects may
result in injury while maneuvering or
transporting system.
• Injury to operator from moving the
console
Acoustic Output Hazard • ALARA, the use of

• Patient injury or tissue damage from power output following
ultrasound radiation the ‘as low as
reasonably achievable’
principle
Explosion Hazard • Flammable anesthetic

Describes precautions necessary to
prevent the risk of injury through
explosion hazard.
• Risk of explosion if used in the
presence of flammable anesthetics
Fire and Smoke Hazard • Replacing fuses

• Patient/operator injury or adverse • Outlet guidelines
reaction from fire or smoke
• Patient/operator injury from explosion
and fire

Introduction/Safety
Important Safety Considerations
The following topic headings (Patient Safety, Equipment and

Personnel Safety) are intended to make the equipment operator
aware of particular hazards associated with the use of this
equipment and the extent to which injury can occur if
precautions are not observed. Additional precautions may be
provided throughout the manual.
CAUTION Improper use can result in serious injury. The use of the system
outside the described conditions or intended use, and
disregarding safety related information is considered abnormal
use. The manufacturer is not liable for damage caused by
abnormal use of the device.
The operator must be thoroughly familiar with the instructions
and potential hazards involving ultrasound examination before
attempting to use the device. Training assistance is available
from GE if needed.

Safety Precautions
Patient Safety
Related Hazards
WARNING The concerns listed can seriously affect the safety of patients
undergoing a diagnostic ultrasound examination.
Patient identification
Always include proper identification with all patient data and
verify the accuracy of the patient's name and ID numbers when
entering such data. Make sure correct patient ID is provided on
all recorded data and hard copy prints. Identification errors could
result in an incorrect diagnosis.
The ultrasound system is not meant for long term storage of
patient data or images. Customers are responsible for the
system data and a regular backup is highly recommended.
It is advisable to back up system data prior to any service
repairs to the hard drive. It is always possible during system
failure and repair to lose patient data. GE will not be held
responsible for the loss of this data.

Introduction/Safety
Diagnostic information
The images and calculations provided by the system are
intended for use by competent operators, as a diagnostic tool.
They are explicitly not to be regarded as the sole, irrefutable
basis for clinical diagnosis. Operators are encouraged to study
the literature and reach their own professional conclusions
regarding the clinical utility of the system.
The operator should be aware of the product specifications, and
of the system accuracy, and stability limitations. These
limitations must be considered before making any decision
based on quantitative values. If in doubt, consult the nearest GE
Ultrasound Service Office.
Equipment malfunction or incorrect settings can result in
measurement errors or failure to detect details within the image.
The equipment operator must become thoroughly familiar with
the equipment operation in order to optimize its performance
and recognize possible malfunctions. Applications training is
available through a local GE representative. Added confidence
in the equipment operation can be gained by establishing a
quality assurance program.
CAUTION Allowing the machine to transmit acoustic output with the probe
not in use (or in its holder) can cause the transducer to build up
heat.
CAUTION The system provides calculations (e.g estimated fetal weight)

and charts based on published scientific literature. Selection of
the appropriate chart and clinical interpretation of calculations
and charts is the sole responsibility of the operator. The
operator must consider contraindications for the use of a
calculation or chart as described in scientific literature. The
diagnosis, decision for further examination and medical
treatment must be performed by qualified personnel following
good clinical practice.
CAUTION Be certain to ensure privacy of patient information data.

Safety Precautions
Mechanical hazards
The use of damaged probes or improper use and manipulation
of intracavity probes can result in injury or increased risk of
infection. Inspect probes often for sharp, pointed, or rough
surface damage that could cause injury or tear protective
barriers. Become familiar with all instructions and precautions
provided with special purpose probes.
Electrical A damaged probe can also increase the risk of electric shock if
Hazard conductive solutions come in contact with internal live parts.
Inspect probes often for cracks or openings in the housing and
holes in and around the acoustic lens or other damage that
could allow liquid entry. Become familiar with the probes use
and care precautions outlined in Probes and Biopsy.
CAUTION Ultrasound transducers are sensitive instruments which can

easily be damaged by rough handling. Take extra care not to
drop transducers and avoid contact with sharp or abrasive
surfaces. A damaged housing, lens, or cable can result in
patient injury or serious impairment of operation.
WARNING To avoid risk of electric shock, this equipment must only be

connected to a supplymains with protective earth.

Introduction/Safety
Scanner and electrosurgical units
CAUTION DO NOT use high-frequency surgical equipment with the

Venue 50.
ALARA
CAUTION Ultrasound can produce harmful effects in tissue and

potentially result in patient injury. Always minimize exposure
time and keep ultrasound levels low when there is no medical
benefit. Use the principle of ALARA (As Low As Reasonably
Achievable), increasing output only when needed to obtain
diagnostic image quality. Observe the acoustic output display
and be familiar with all controls affecting the output level. See
the Bioeffects section of the Acoustic Output chapter in the
Advanced Reference Manual for more information.
Training
It is recommended that all operators receive proper training in
applications before performing them in a clinical setting. Please
contact a local GE representative for training assistance.

Safety Precautions
Equipment and Personnel Safety

The concerns listed below can seriously affect the safety of
equipment and personnel during a diagnostic ultrasound
examination.
Do not use this equipment if a safety problem is known to exist.
Have the unit repaired and performance verified by qualified
service personnel before returning to use.
Related Hazards
WARNING This equipment contains dangerous voltages that are capable

of serious injury or death.
If any defects are observed or malfunctions occur, stop
operating the equipment and perform the proper action for the
patient.
There are no operator serviceable components inside the
console. Refer all servicing to the repair center.
Ensure that unauthorized personnel do not tamper with the
unit.
Electrical To avoid injury:

Hazard • Do not remove protective covers. No operator serviceable
parts are inside. Refer servicing to qualified service
personnel.
• To assure adequate grounding, connect the attachment
plug to a reliable (hospital grade) grounding outlet (having
equalization conductor ).
• Never use any adaptor or converter of a
three-prong-to-two-prong type to connect with a main
power plug. The protective earth connection will loosen.
• Be sure that liquid does not drip into the console.
• In North America, a 220-240V installation requires the use
of a center-tapped AC power source.

Introduction/Safety
Related Hazards (continued)
Smoke & The system must be supplied from an adequately rated

Fire Hazard electrical circuit. The capacity of the supply circuit must be as
specified.
WARNING Only approved and recommended peripherals and accessories

should be used.
All peripherals and accessories must be securely mounted to
the Venue 50 or Docking Station/Cart.
WARNING Venue 50 is not intended to be used as a storage device;

backup of the patient and image database is your institution’s
responsibility.GE is NOT responsible for any lost patient
information or for lost images.
Explosion Risk of explosion if used in the presence of flammable

Hazard anesthetics.
WARNING Connecting electrical equipment to multiple socket-outlet

effectively leads to creating a mechanical system, and can
result in a reduced level of safety.

Safety Precautions
Explosion Never operate the equipment in the presence of flammable or

Hazard explosive liquids, vapors or gases. Malfunctions in the unit or
sparks generated by fan motors, can electrically ignite these
substances. Operators should be aware of the following points
to prevent such explosion hazards.
• If flammable substances are detected in the environment,
do not plug in or turn on the system.
• If flammable substances are detected after the system has
been turned on, do not attempt to turn off the unit, or to
unplug it.
• If flammable substances are detected, evacuate and
ventilate the area before turning off the unit.
CAUTION Peripheral devices that use their own AC power source

CANNOT be attached to the Venue 50. DO NOT connect the
peripheral device’s power cord into the Venue 50 system.
Use a USB printer cable that is less than 3 meters (9.8 feet) in
length.
CAUTION Do not use this equipment if a safety problem is known to exist.

Have the unit repaired and performance verified by qualified
service personnel before returning to use.

Introduction/Safety
Biological For patient and personnel safety, be aware of biological

Hazard hazards while performing invasive procedures. To avoid the
risk of disease transmission:
• Use protective barriers (gloves and probe sheaths)
whenever possible. Follow sterile procedures when
appropriate.
• Thoroughly clean probes and reusable accessories after
each patient examination and disinfect or sterilize as
needed. Refer to Probes and Biopsy for probe use and
care instructions.
• Follow all infection control policies established by your
office, department or institution as they apply to personnel
and equipment.
CAUTION Contact with natural rubber latex may cause a severe

anaphylactic reaction in persons sensitive to the natural latex
protein. Sensitive operators and patients must avoid contact
with these items. Refer to package labeling to determine latex
content and FDA’s March 29, 1991 Medical Alert on latex
products.

Safety Precautions
CAUTION To avoid injury or system damage, NEVER place any object or

liquid on the operator panel.
CAUTION Archived data is managed at the individual sites. Performing

data backup (to any device) is recommended.
CAUTION DO NOT use high-frequency surgical equipment with the

Venue 50.
CAUTION Make sure to verify the media after writing of data, including
Save, Backup and Restore.
Before deleting a patient or image from the patient screen,
make sure you have saved the data and verify that the media
transfer of data was successful.
CAUTION DO NOT touch the patient and any of the connectors on the
ultrasound unit simultaneously, including ultrasound probe
connectors.
DO NOT touch the conducting parts of the USB, ethernet,
video, audio cables when connecting equipment to the unit.

Introduction/Safety
General Caution
CAUTION Standard maintenance must be performed by authorized

service personnel during the lifetime of the product (7 years).
CAUTION Proceed cautiously when crossing door or elevator thresholds

with Docking Cart. Use the handle to push/pull the system,
e.g., do not use the Venue 50. Failure to do so may cause
serious injury or system damage.
CAUTION The maximum capacity load is 8kg (17.6lbs) for the Printer
Shelf (1) and 2kg (4.4lbs) for the Accessories Shelf (2). Please
refer to the figure below.
Figure 1-1. Capacity Load

Safety Precautions
EMC (Electromagnetic Compatibility)

NOTE: This equipment generates, uses and can radiate radio
frequency energy. The equipment may cause radio frequency
interference to other medical and non-medical devices and radio
communications. To provide reasonable protection against such
interference, this product complies with emissions limits for a
Group 1, Class A Medical Devices Directive as stated in EN
60601-1-2. However, there is no guarantee that interference will
not occur in a particular installation.
NOTE: If this equipment is found to cause interference (which may be
determined by turning the equipment on and off), the operator
(or qualified service personnel) should attempt to correct the
problem by one or more of the following measure(s):
• reorient or relocate the affected device(s)
• increase the separation between the equipment and the
affected device
• power the equipment from a source different from that of the
affected device
• consult the point of purchase or service representative for
further suggestions.
NOTE: The manufacturer is not responsible for any interference caused
by using other than recommended interconnect cables or by
unauthorized changes or modifications to this equipment.
Unauthorized changes or modifications could void the operators’
authority to operate the equipment.
NOTE: To comply with the regulations on electromagnetic interference
for a Class A FCC Device, all interconnect cables to peripheral
devices must be shielded and properly grounded. Use of cables
not properly shielded and grounded may result in the equipment
causing radio frequency interference in violation of the FCC
regulations.

Introduction/Safety
EMC Performance
All types of electronic equipment may characteristically cause

electromagnetic interference with other equipment, either
transmitted through air or connecting cables. The term EMC
(Electromagnetic Compatibility) indicates the capability of
equipment to curb electromagnetic influence from other
equipment and at the same time not affect other equipment with
similar electromagnetic radiation from itself.
Proper installation following the service manual is required in
order to achieve the full EMC performance of the product.
The product must be installed as stipulated in “Notice upon
Installation of Product” section.
In case of issues related to EMC, please call your service
personnel.
The manufacturer is not responsible for any interference caused
by using other than recommended interconnect cables or by
unauthorized changes or modifications to this equipment.
Unauthorized changes or modifications could void the operators’
authority to operate the equipment.
CAUTION Do not use devices which intentionally transmit RF signals

(cellular phones, transceivers, or radio controlled products),
other than those supplied by GE (wireless microphone,
broadband over power lines, for example) unless intended for
use with this system, in the vicinity of this equipment as it may
cause performance outside the published specifications.
Keep power to these devices turned off when near this
equipment.
The medical staff in charge of this equipment is required to
instruct technicians, patients and other people who may be
around this equipment to fully comply with the above
requirement.

Safety Precautions
EMC Performance (continued)
Portable and mobile radio communications equipment (e.g.

two-way radio, cellular/cordless telephones and similar
equipment) should be used no closer to any part of this system,
including cables, than determined according to the following
method:
Table 1-2: Portable and mobile radio communications equipment distance
requirements
Frequency Range: 150 kHz - 80 MHz 80 MHz - 800 MHz 800 MHz - 2.5 GHz
Calculation Method: d=[3.5/V1] square root d = [3.5/E1] square root d = [7/E1] square root of
of P of P P
Where: d= separation distance in meters, P = rated power of the transmitter, V1=compliance value for
conducted RF, E1 = compliance value for radiated RF
If the maximum The separation distance in meters should be

transmitter power in
watts is rated
5 2.6 2.6 5.2
20 5.2 5.2 10.5
100 12.0 12.0 24.0

Introduction/Safety
General Notice
1. Designation of peripheral equipment connectable to this

product.
The equipment indicated in Chapter 6 can be hooked up to
the product without compromising its EMC performance.
Avoid using equipment not designated in the list. Failure to
comply with this instruction may result in poor EMC
performance of the product.
2. Notice against user modification
The operator should never modify this product. User
modifications may cause degradation in EMC performance.
Modification of the product includes changes in:
a. Cables (length, material, wiring, etc.)
b. System installation/layout
c. System configuration/components
d. Securing system parts (cover open/close, cover
screwing)

Safety Precautions
Peripheral Update for EC countries
The following is intended to provide the operators in EC

countries with updated information concerning the connection of
the Venue 50 to image recording and other devices or
communication networks.
Peripheral used in The Venue 50 has been verified for overall safety, compatibility
the patient and compliance with the image recording devices listed in
environment ‘Supplies/Accessories’ on page 6-36.
The Venue 50 may also be used safely while connected to
devices other than those recommended above if the devices
and their specifications, installation, and interconnection with the
system conform to the requirements of IEC/EN 60601-1.
CAUTION The connection of equipment or transmission networks other

than as specified in the user instructions can result in an
electric shock hazard or equipment malfunction. Substitute or
alternate equipment and connections requires verification of
compatibility and conformity to IEC/EN 60601-1 by the installer.
Equipment modifications and possible resulting malfunctions
and electromagnetic interference are the responsibility of the
owner.
General precautions for installing an alternate off-board, remote

device or a network would include:
• The added device(s) must have appropriate safety standard
conformance and CE Marking.
• There must be adequate mechanical mounting of the device
and stability of the combination.
• Risk and leakage current of the combination must comply
with IEC/EN 60601-1.
• Electromagnetic emissions and immunity of the combination
must conform to IEC/EN 60601-1-2.

Introduction/Safety
Declaration of Emissions
This system is suitable for use in the following environments.

The operator must assure that the system is used according to
the specified guidance and only in the electromagnetic
environment listed below.
Table 1-3: Declaration of Emissions
Guidance and manufacturer’s declaration - electromagnetic emissions
The system is intended for use in the electromagnetic environment specified below. The
operator of the system should assure that it is used in such an environment.
Emission Type Compliance Electromagnetic Environment
RF Emissions Group 1 This system uses RF energy only for its internal function.
CISPR 11 Therefore, its RF emissions are very low and are not likely to
cause any interference in nearby electronic equipment.
RF Emissions Class A This system is suitable for use in all establishments, other than
CISPR 11 domestic establishments and those directly connected to the
public low-voltage power supply network that supplies buildings
Harmonic Class A used for domestic purposes, provided the following warning is
Emissions heeded:
IEC 61000-3-2 WARNING: This system is intended for use by healthcare
professionals only. This system may cause radio interference or
Voltage Complies
may disrupt the operation of nearby equipment. It may be
Fluctuations/Flicker
necessary to take mitigation measures, such as re-orienting or
Emissions relocating the system or shielding the location.
IEC 61000-3-3

Safety Precautions
Declaration of Immunity
This system is suitable for use in the following environments.

The operator must assure that the system is used according to
the specified guidance and only in the electromagnetic
environment listed below.
Table 1-4: Declaration of Immunity
Immunity Equipment Regulatory EMC Environment and

Type Capability Acceptable Level Guidance
IEC 61000-4-2 ± 6 kV contact ± 6 kV contact Floors should be wood, concrete, or

Static discharge ceramic tile. If floors are covered with
(ESD) ± 8 kV air ± 8 kV air synthetic material, the relative
humidity should be at least 30%.
IEC 61000-4-4 ± 2 kV for mains ± 2 kV for mains Mains power quality should be that of
Electrical fast a typical commercial and/or hospital
transient/burst ± 1 kV for SIP/ ± 1 kV for SIP/SOP environment. If the operator requires
SOP continued operation during power
mains interruptions, it is
IEC 61000-4-5 ± 1 kV differential ± 1 kV differential recommended that the system be
Surge Immunity powered from a UPS or a battery.
± 2 kV common ± 2 kV common NOTE: UT is the a.c. mains voltage
prior to application of the test level.
IEC 61000-4-11 < 50T (> 95% dip) < 50T (> 95% dip) for
Power frequency magnetic fields
Voltage dips, for 0.5 cycle; 0.5 cycle;
should be at levels characteristic of a
short 400T (60 0ip) for 5 400T (60 0ip) for 5
typical location in a typical commercial
interruptions and cycles; cycles; and/or hospital environment.
voltage 700T (30 0ip) for 700T (30 0ip) for 25 Separation distance to radio
variations on
25 cycles; cycles; communication equipment must be
mains supply
< 50T (>95% dip) < 50T (>95% dip) for 5 maintained according to the method
for 5 sec sec below. Interference may occur in the
vicinity of equipment marked with the
IEC 61000-4-8 3 A/m 3 A/m symbol:
Power
frequency (50/
60 Hz) magnetic
field Image degradation or interference
may occur due to conducted RF noise
IEC 61000-4-6 3 VRMS 3 VRMS on the equipment mains power supply
Conducted RF 150 kHz - 80 MHz 150 kHz - 80 MHz or other signal cable. Such
interference is easily recognized and
IEC 61000-4-3 3 V/m 3 V/m distinguishable from patient anatomy
Radiated RF 80 MHz - 2.5 GHz 80 MHz - 2.5 GHz and physiological waveforms.
Interference of this type may delay the
examination without affecting
diagnostic accuracy. Additional mains/
signal RF isolation or filtering may be
needed if this type interference occurs
frequently.
NOTE: These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflection from structures, objects, and people. If noise generated from other electronic
equipment is near the probe’s center frequency, noise may appear on the image. Good power line isolation
is required.

Introduction/Safety
Patient Environmental Devices
Figure 1-2. Patient Environmental Devices
1. Top side of Venue 50: SD Card socket and 1 USB port

2. Left side of Venue 50: Lithium-ion battery port
3. Left side of Docking Station/Cart:
• 1 LAN port
• 3 Master USB ports
• 1 HDMI port
4. Left side of Docking Cart: Printer AC power input socket
5. Bottom of Venue 50: Docking port
6. Right side of Venue 50: Probe port
7. Right side of Docking Station: AC power input socket
Bottom of Docking Cart: AC power input socket

Safety Precautions
Acceptable Devices
The Patient Environmental Devices shown on the previous page

are specified to be suitable for use within the PATIENT
ENVIRONMENT.
CAUTION DO NOT connect any probes or accessories without approval

by GE within the PATIENT ENVIRONMENT.
See ‘Peripheral Update for EC countries’ on page 1-25 for
more information.
Unapproved Devices
CAUTION DO NOT use unapproved devices.

If devices are connected without the approval of GE, the
warranty will be INVALID.
Any device connected to the Venue 50 must conform to one or
more of the requirements listed below:
1. IEC standard or equivalent standards appropriate to
devices.
2. The devices shall be connected to PROTECTIVE EARTH
(GROUND).
Accessories, Options, Supplies
CAUTION Unsafe operation or malfunction may result. Use only the

accessories, options and supplies approved or recommended
in these instructions for use.

Introduction/Safety
Acoustic Output
Located on the upper right section of the system display monitor,
the acoustic output display provides the operator with real-time
indication of acoustic levels being generated by the system. See
the Acoustic Output chapter in the Advanced Reference Manual
for more information. This display is based on NEMA/AIUM
standards for real-time display of thermal and mechanic
acoustic output indices on diagnostic ultrasound equipment.
Acoustic Output Display Specifications
The display consists of three parts: Thermal Index (TI),

Mechanical Index (MI), and a relative Acoustic Output (AO)
value. Although not part of the NEMA/AIUM standard, the AO
value informs the operator of where the system is operating
within the range of available output.
The TI and MI are displayed at all times. The TI and MI display
starts at a value of 0.0 and increments in steps of 0.1.
Thermal Index
Depending on the examination and type of tissue involved, the
TI parameter will be one of three types:
• Soft Tissue Thermal Index (TIS). Used when imaging soft
tissue only, it provides an estimate of potential temperature
increase in soft tissue.
• Bone Thermal Index (TIB). Used when bone is near the
focus of the image as in the third trimester OB examination,
it provides an estimate of potential temperature increase in
the bone or adjacent soft tissue.
• Cranial Bone Thermal Index (TIC). Used when bone is
near the skin surface as in transcranial examination, it
provides an estimate of potential temperature increase in
the bone or adjacent soft tissue.
Mechanical Index
MI recognizes the importance of non-thermal processes,
cavitation in particular, and the Index is an attempt to indicate
the probability that they might occur within the tissue.

Safety Precautions
Acoustic Output Display Specifications (continued)
Changing the Thermal Index Type

You can select the displayed TI type on Utility -> Image. This
preset is application dependent so each application could
specify a different TI type.
TI and MI Display Accuracy

When display MI >= 0.6, TI >= 3.6, the displayed values of MI
and TI is not lower than 50% or higher than 150% of the
measured values.
When display MI < 0.6, TI < 3.6, the absolute error of MI <= 0.3,
the absolute error of TI <= 1.8.
Controls Affecting Acoustic Output
The potential for producing mechanical bioeffects (MI) or

thermal bioeffects (TI) can be influenced by certain controls.
Direct. The Acoustic Output control has the most significant
effect on Acoustic Output.
Indirect. Indirect effects may occur when adjusting controls.
Controls that can influence MI and TI are detailed under the
Bioeffects portion of each control in the Optimizing the Image
chapter.
Always observe the Acoustic Output display for possible effects.

Introduction/Safety
Best practices while scanning
HINTS Raise the Acoustic Output only after attempting image

optimization with controls that have no effect on Acoustic
Output, such as Gain and TGC.
WARNING Be sure to have read and understood control explanations for

each mode used before attempting to adjust the Acoustic
Output control or any control that can effect Acoustic Output.
Acoustic Use the minimum necessary acoustic output to get the best
Output diagnostic image or measurement during an examination.
Hazard Begin the exam with the probe that provides an optimum focal
depth and penetration.
Acoustic Output Default Levels
In order to assure that an exam does not start at a high output

level, the Venue 50 initiates scanning at a reduced default
output level. This reduced level preset depends upon the exam
application and probe selected.
To modify acoustic output, go to Utility->Image->User Define,
then adjust the acoustic output level in AO select box.

Device Labels
Device Labels
Icon Description
The following table describes the purpose and location of safety
labels and other important information provided on the
equipment.
Table 1-5: Label Icons
Label/Icon Purpose/Meaning Location
Identification and Rating Plate • Manufacture’s name and address Rating Plate Label.
• Date of manufacture ‘Warning label locations’ on
• Model and serial numbers page 1-33
• Electrical ratings (Volts, Amps,
phase, and frequency)
Type/Class Label Used to indicate the degree of safety Rating Plate Label
or protection.
IP Code (IPX8) Indicates the degree of protection Footswitch

IPX8: MKF 2 1S/1S-MED HID provided by the enclosure per
GP 26 IEC60529. IPX8 can be used in an
operating room environment.
Authorized European Representative

address
United States only

Prescription Requirement label
Type BF Applied Part (man in the box) Probe connector and rating
symbol is in accordance with IEC plate
60878-02-03.
General Warning Various

Introduction/Safety
“Consult accompanying documents” is Various

intended to alert the operator to refer
to the operator manual or other
instructions when complete
information cannot be provided on the
label.
“CAUTION” - Dangerous voltage (the Various

lightning flash with arrowhead) is used
to indicate electric shock hazards.
“ON” indicates the power on position See the Console Overview

of the power switch. section for location
CAUTION: This Power Switch DOES information.
NOT ISOLATE Mains Supply.
“Protective Earth” indicates the • Inside of AC adapter with

protective earth (grounding) terminal. docking station
• Docking cart
“Equipotentiality” indicates the Docking Cart

terminal to be used for connecting
equipotential conductors when
interconnecting (grounding) with other
equipment.
Connection of additional protective
earth conductors or potential
equalization conductors is not
necessary in most cases and is only
recommended for situations involving
multiple equipment in a high-risk
patient environment to provide
assurance that all equipment is at the
same potential and operates within
acceptable leakage current limits. An
example of a high-risk patient would
be a special procedure where the
patient has an accessible conductive
path to the heart such as exposed
cardiac pacing leads. IEC60417-5021
NRTL Listing and Certification Mark is Back of Venue 50

used to designate conformance to
nationally recognized product safety
standards. The Mark bears the name
and/or logo of the testing laboratory,
product category, safety standard to
which conformity is assessed and a
control number.

Device Labels
This symbol indicates that waste Rating Plate

electrical and electronic equipment
must not be disposed of as unsorted
municipal waste and must be collected
separately. Please contact an
authorized representative of the
manufacturer for information
concerning the decommissioning of
your equipment.
No hazardous substance, above the Bottom

maximum concentration value, is
present. Maximum concentration
values for electronic information
products, as set by the People’s
Republic of China Electronic Industry
Standard SJ/T11364-2006,Include the
hazardous substances of lead,
mercury, hexavalent chromium,
cadmium, polybrominated biphenyl
(PBB), and polybrominated diphenyl
ether (PBDE)
Indicates the presence of hazardous Rating Plate

substance(s) above the maximum
concentration value. Maximum
concentration values for electronic
information products, as set by the
People’s Republic of China Electronic
Industry Standard SJ/T11364-2006,
include the hazardous substances of
lead, mercury, hexavalent chromium,
cadmium, polybrominated biphenyl
(PBB), and polybrominated diphenyl
ether (PBDE). “10” indicates the
number of years during which the
hazardous substance(s) will not leak
or mutate so that the use of this
product will not result in any severe
environmental pollution, bodily injury,
or damage to any assets.
GOST symbol: Russia Regulatory Bottom

Country Clearance. Note: Only after Russian
regulatory registration is
complete, this label will be
located on the console rating
plate.

Introduction/Safety
INMETRO Certification: TUV Back of the system

Rheinland Brazil Note: Only after Brazilian
regulatory registration is
complete, this label will be
located on the console rating
plate.
Do not put anything weighed over 5kg Printer shelf of Docking Cart
(11 lbs) on the shelf.
Do not push the system Back of Docking Cart and

Rating plate
Do not step on the system Base chassis covers of

Docking Cart

Device Labels
Warning label locations

Venue 50 warning labels are provided in English.
Figure 1-3. Label location explanations
Table 1-6: Label Location Explanations
1. The CE Mark of Conformity indicates this 4. Prescription Device (For U.S.A. Only)
equipment conforms with the Council Directive 5. Warning of Gender Determination
93/42/EEC. 6. CISPR CAUTION: The Venue 50 conforms to
2. Possible shock hazard. Do not remove covers the CISPR11, Group 1, Class A of the
or panels. No operator serviceable parts are international standard for Electromagnetic
inside. Refer servicing to qualified service disturbance characteristics.
personnel.
3. “Consult accompanying documents” is intended
to alert the operator to refer to the operator
manual or other instructions when complete
information cannot be provided on the label.

Introduction/Safety
Warning label locations (continued)

Table 1-7: Rating Plate Explanations
Date of manufacture: The date could be a year, year and

month, or year, month and day, as appropriate. See ISO 8601
for date formats.
Catalog or model number
REF
Serial number
SN
Direct Current: For products to be powered from a DC
supply
Description
Model
Input
Output
Made in China
Made by Coretronic
Ultrasound Diagnostic Device
Only for use with Venue 50
Only for use with Docking Cart or Docking Station

Device Labels
Figure 1-4. Docking Station Label
Figure 1-5. Docking Station label location

Introduction/Safety
Figure 1-6. Docking Cart warning label
Figure 1-7. Docking Cart label location

Device Labels
Figure 1-8. Battery Label
Table 1-8: Icons Explanations
Keep the battery away from fire and other heat sources.
Do not disassemble or alter the battery.
The battery can be recharged.

Introduction/Safety

Chapter 2
Preparing the System for Use
Describes the site requirements, console overview,

system positioning/transporting, powering on the
system, adjusting the display monitor, probes and
operator controls.

Site Requirements
Introduction
NOTE: Only qualified physicians or sonographers should perform
ultrasound scanning on human subjects for medical diagnostic
reasons. Request training, if needed.
The Venue 50 does not contain any operator serviceable
internal components. Ensure that unauthorized personnel do not
tamper with the unit.
Perform regular preventive maintenance. See ‘System Care and
Maintenance’ on page 6-13 for more information.
Maintain a clean environment. Turn off, and if possible,
disconnect the system before cleaning the unit. See ‘Cleaning
the system’ on page 6-16 for more information.

Site Requirements
Before the system arrives

NOTICE This medical equipment is approved, in terms of the prevention
of radio wave interference, to be used in hospitals, clinics and
other institutions which are environmentally qualified. The use of
this equipment in an inappropriate environment may cause
some electronic interference to radios and televisions around
the equipment.
Ensure that the following is provided for the new system:
• A separate power outlet with a 6 amp circuit breaker for
220-240 VAC or a 10 amp circuit breaker for 100-120 VAC.
NOTE: This is for the Docking Station/Cart.
• Take precautions to ensure that the console is protected
from electromagnetic interference.
Precautions include:
• Operate the console at least 15 feet away from motors,
typewriters, elevators, and other sources of strong
electromagnetic radiation.
• Operation in an enclosed area (wood, plaster or
concrete walls, floors and ceilings) helps prevent
electromagnetic interference.
• Special shielding may be required if the console is to be
operated in the vicinity of radio broadcast equipment.

Environmental Requirements
The system should be operated, stored, or transported within
the parameters outlined below. Either its operational
environment must be constantly maintained or the unit must be
turned off.
Table 2-1: System Environmental Requirements
Operational Storage Transport
Temperature 3 - 40°C -5 - 50°C -5 - 50°C

37 - 104°F 23 - 122°F 23 - 122°F
Humidity 30 - 80% non-condensing 10 - 90% non-condensing 10 - 90% non-condensing
Pressure 700 - 1060hPa 700 - 1060hPa 700 - 1060hPa
Acclimation Time
After being transported, the unit requires one hour for each 2.5
degree increment when its temperature is below 10°C or above
40°C.
Table 2-2: System Acclimation Time Chart
°C 60 55 50 45 40 35 30 25 20 15 10
°F 140 131 122 113 104 95 86 77 68 59 50
hours 8 6 4 2 0 0 0 0 0 0 0
°C 5 0 -5 -10 -15 -20 -25 -30 -35 -40
°F 41 32 23 14 5 -4 -13 -22 -31 -40
hours 2 4 6 8 10 12 14 16 18 20

Console Overview
Console Overview
Console graphics
The following are illustrations of the console:
Figure 2-1. Venue 50 system (with Docking Station)
1. Venue 50
2. Docking Station

Console graphics (continued)
Figure 2-2. Venue 50 views
1. Battery 3. Docking Port

2. SD Card Socket and USB Port 4. Probe Port
CAUTION DO NOT push objects into air vents of system. Doing so can
cause fire or electric shock by shorting out interior components.

Console Overview
Docking Cart
Figure 2-3. Docking Cart
1. Docking
2. Plastic shelf - for accessories and disposals
3. Pedal
4. Wheels brake pedal - for Cart brakes
5. Cart Handle
6. Printer shelf (option)
7. 3-probe port box (option)
8. Multi-probe holder (option)
9. Basket - for accessories and disposals (option)
CAUTION Be sure to lock the wheels before Venue 50 is mounted to the

Docking Cart.

Battery
The lithium ion battery provides power when an AC power

source is not available. A battery in the battery bay is standard
with the Venue 50. Lithium ion batteries last longer than
conventional batteries and do not require replacement as often.
You can expect 40 minutes of battery life with a single fully
charged battery.
The lithium ion technology used in your Venue 50’s battery is
significantly less hazardous to the environment than the lithium
metal technology used in some other batteries (such as watch
batteries). Used batteries should not be placed with common
household waste products. Contact local authorities for the
location of a chemical waste collection program nearest you.
WARNING • The battery has a safety device. Do not disassemble or

alter the battery.
• Charge and discharge the batteries only when the ambient
temperature is between 3°C and 40°C (37°F and 104°F).
• DO NOT short-circuit the battery by directly connecting the
negative terminals with metal objects.
• DO NOT heat the battery or discard it in a fire.
• DO NOT expose the battery to temperature over 50°C
(122°F). Keep it away from fire and other heat sources.
• DO NOT charge the battery near a heat source, such as a
fire or heater.
• DO NOT leave the battery in direct sunlight.
• DO NOT pierce the battery with a sharp object, hit it, or
step on it.
• DO NOT use a damaged battery.
• DO NOT solder a battery.
• DO NOT connect the battery to an electrical power outlet.

Console Overview
Battery (continued)
WARNING If the Venue 50 is not being used on a monthly basis, the

battery needs to be removed during the lengthy non-use
period.
CAUTION To avoid the battery bursting, igniting, or fumes from the battery
causing equipment damage, observe the following precautions:
• DO NOT immerse the battery in water or allow it to get wet.
• DO NOT put the battery into a microwave oven or
pressurized container.
• If the battery leaks or emits an odor, remove it from all
possible flammable sources.
• If the battery emits an odor or heat, is deformed or
discolored, or in a way appears abnormal during use,
recharging or storage, immediately remove it and stop
using it. If you have any questions about the battery,
consult GE or your local representative.
• Short term (less than one month) storage of battery pack:
• Store the battery in a temperature range between -5°C
(23°F) and 50°C (122°F).

Battery (continued)
CAUTION • Long term (3 months or more) storage of battery pack:

• Store the battery in a temperature range between -5°C
(23°F) and 50°C (122°F)
• Upon receipt of the Venue 50 and before first time
usage, it is highly recommended that the customer
performs one full discharge/charge cycle. If the battery
has not been used for 2 months or more, the customer
is recommended to perform one full discharge/charge
cycle. It is also recommended to store the battery in a
shady and cool area with FCC (full current capacity).
• One full discharge/charge cycle process:
1. Full discharge of battery to let the Venue 50
automatically shut down.
2. Charge the Venue 50 to 100% FCC (full current
capacity).
3. Discharge of Venue 50 for complete shut down
(takes one hour for discharge).
• When storing batteries for more than 6 months, charge
the batteries at least once every 6 months to prevent
leakage and deterioration in performance.
• Use only GE approved batteries.

Console Overview
Battery (continued)
View current battery status

When the system is running, there is a battery icon in the upper
right corner of the screen. It’s current capacity in percent
appears ”current capacity (unit: percent)”.
Figure 2-4. Battery icon
When the battery is charging

If the battery is charging, the following icon displays:
Figure 2-5. Battery charging
Battery power low warning

If the battery is in use and the battery power is low, the battery
icon becomes orange, with a warning message: “Battery is
critical, system will shut down in 1 minute.” displays.
Figure 2-6. Low battery power warning
AC power only/battery charging complete

If the battery is fully charged or the system is using AC Power
only, the following icon displays:
Figure 2-7. AC power only or battery charging complete

Battery (continued)
Battery Replacement
1. Lay the Venue 50 face down on a stable, smooth surface to
avoid scratching the LCD.
2. Pull off the battery cover and remove the battery pack.
Figure 2-8. Battery replacement
NOTE: Battery can be replaced on Docking Station/Cart.
View battery capacity

Press the button on the battery; the LED indicates the remaining
battery capacity.
Figure 2-9. View battery capacity

Console Overview
Peripheral/Accessory Connection
Peripheral/Accessory Connector Panel of Docking Station/Cart
Venue 50 System peripherals and accessories can be properly

connected using the side panels of the Docking Station/Cart.
CAUTION Each outer (case) ground line of peripheral/accessory

connectors are earth grounded.
Signal ground lines are not isolated.
CAUTION For compatibility reasons, use only GE approved probes,

peripherals or accessories.
DO NOT connect any probes or accessories without approval
by GE.

Peripheral/Accessory Connector Panel of Docking Station/Cart

(continued)
Figure 2-10. Docking Connector Panel
Docking Station provides DC power to Venue 50 and charging

function to battery.
1. Probe Holder (Holder on each side)
2. AC Power Indicator
3. Battery Charging Indicator
4. AC Power Input Socket
5. LAN Port
6. 3 USB Ports (for peripherals connection)
7. HDMI Port (for external monitor connection)
NOTE: Without AC power, only the first USB port (from top to bottom) is
available.
NOTE: Without AC power, LAN port, the second and third USB ports
and HDMI port are not available.
CAUTION The connection of equipment or transmission networks other

than as specified in these instructions can result in electric
shock hazard. Alternate connections will require verification of
compatibility and conformity to IEC/EN 60601-1 by the installer.

Console Overview
Peripherals Connection
1. Insert the SD Card into the SD Card Socket on top of the

system. Ensure the labeled side is facing the front.
Figure 2-11. Insert SD Card
2. Connect the USB cable from the printer to the USB port of
Docking Station/Cart. Connect the printer’s power cord and
power on the printer.
Figure 2-12. B/W Printer Connection

Peripherals Connection (continued)
3. Connect the USB memory stick to the USB port of Docking

Station/Cart.
Figure 2-13. USB Memory Stick Connection
4. Connect the external monitor to the HDMI port of the

Docking Station/Cart.
Figure 2-14. HDMI Connection

Console Overview
5. Connect the Wireless Network Adapter to the USB port of

the Docking Station/Cart.
Figure 2-15. Wireless Network Adapter Connection
6. Connect the footswitch to the USB port of the Docking

Station/Cart.
Figure 2-16. Footswitch Connection

7. Connect the barcode reader to the USB port of the Docking

Station/Cart.
Figure 2-17. Barcode Reader Connection
To set up the barcode reader, please follow the steps below:

• Connect barcode reader to the system.
• Go to Utility -> Settings -> USB Accessories to set
Barcode Reader on.
• Scan the three bar code below in order, from top to
bottom. First scan the bar
code, then scan . This resets the
scanner to the factory default settings. Finally, scan the
bar code. It programs a carriage return (CR)
suffix. Now the Barcode Reader is ready for use.
Figure 2-18. Barcode

Console Overview
Mount Venue 50 to Docking Station/Cart

1. Place the Docking Station and system on a stable surface.
2. Carefully pick up the system. Align the port on the Venue 50
with the docking port and carefully push into place.
Figure 2-19. Mount to Docking Station/Cart
3. Press the locking lever down until it locks in place.
Figure 2-20. Press the locking lever

Release Venue 50 from the Docking Station/Cart

1. Pull the release trigger. The locking lever pops up and the
Venue 50 can be removed.
Figure 2-21. Release system from Docking Station/Cart
WARNING Please make sure to turn off the Venue 50 before releasing it
from the Docking Station/Cart.

Moving the System

When moving or transporting the system, follow the precautions
below to ensure the maximum safety for personnel, the system,
and other equipment.
Before moving the system
1. Press the Power On/Off switch to power off the system.

2. Unplug the Docking Station/Cart power cord (if the system is
plugged in).
3. Release the Venue 50 from the Docking Station/Cart.
4. Store all probes in their original cases or in soft cloth or foam
to prevent from damage.
5. Store sufficient gel and other essential accessories in the
special storage case.

When moving the system
CAUTION To avoid possible injury and equipment damage:

• Do not let the system strike walls or door frame.
• Limit movement to a slow careful walk.
NOTE: When moving the Docking Cart, be sure the path is clear. Limit
movement to a slow careful walk.
NOTE: Make sure the console is locked in place to avoid damaging the
system due to a fall.
NOTE: Utilize additional care when moving on a steep incline (>5
degrees) or loading the system into vehicle for transport.

Cable management
WARNING To avoid the cables catching on external devices, please

ensure the power cord and probe cables are wrapped properly,
not extended beyond sides of Docking Cart and out of the way
for portables.
• Place probes securely in proper probe holders. Wrap the

probe cables around the probe hooks on sides of the
Docking Cart.
• Place the probe connector which is not used in the plastic
shelf.
• Wrap the power cord around the power cable hook at the
rear panel of the Docking Cart.
NOTE: If the 3-probe port is attached to the system, please see
“3-probe Port User Instructions” for more information.
Figure 2-22. Cable management

Transporting the System

Use extra care when transporting the system using vehicles. In
addition to the instructions used when moving the system (See
‘Moving the System’ on page 2-21 for more information.), also
perform the following:
1. Ensure that the system is firmly secured while inside the
vehicle.
2. Secure system with straps or as directed otherwise to
prevent motion during transport.

Attaching the Security Cable

For extra safety, the Venue 50 may be attached to the docking
station/cart with a security cable as follows.
1. Wrap the cable around an immovable object.
2. Insert the lock into the security slot on the back of the
system.
Figure 2-23. Insert the security lock
NOTE: Be sure that the security lock is rotated to the unlocked

position before inserting the lock.

Attaching the Security Cable (continued)

3. Rotate the key to the locked position.
Figure 2-24. Security cable attached

Powering the System
Powering the System
Connecting and Using the System

To connect the Docking Station/Cart to the electrical supply:
1. Ensure that the wall outlet is of the appropriate type.
2. Push the power plug securely into the wall outlet.
CAUTION Use caution to ensure that the power cable does not
disconnect during system use.
If the system is accidentally unplugged, data may be lost.
WARNING DO NOT use the Venue 50 on plastic foam, paper or similar

type surfaces. The system could overheat and slow down.
Ensure that the Venue 50 is on a sturdy, heat resistant surface.
WARNING To avoid risk of fire, the system power must be supplied from a
separate, properly rated outlet. See ‘Before the system arrives’
on page 2-3 for more information.
Under no circumstances should the AC power plug be altered,
changed, or adapted to a configuration rated less than
specified. Never use additional multiple portable socket-outlets,
an extension cord or an adapter plug.
To help assure grounding reliability, connect to a “hospital
grade” or “hospital only” grounded power outlet.

Connecting and Using the System (continued)
Figure 2-25. Example Plug and Outlet Configurations
1. 100-120 VAC, 1200 VA

Plug and Outlet Configuration
2. 220-240 VAC, 1200 VA
Plug and Outlet Configuration
NOTE: Country-specific power cords are currently available for the
United States, Japan, the United Kingdom, Europe, Denmark,
Switzerland, Israel, India/South Africa, China, Brazil, Australia/
New Zealand, and Argentina.

Powering the System
Power On
Press the Power On/Off switch on top of the system to turn on/
off the system.
Figure 2-26. Power On/Off Switch Location
Press the Power On/Off, then press Lock Screen to lock the
screen.
Figure 2-27. Lock the Screen

LED
Figure 2-28. LED Indicators (Docking Station/Cart)
1. Indicates AC power status. When the Docking Station/Cart

is connecting to AC power, the AC Source LED is lit.
Color: Green
2. Indicates battery status. When the battery is charging, the
Charging LED is lit.
Color: Green
Figure 2-29. LED Indicators (Venue 50)
3. Indicates power status. After pressing the Power On/Off

switch, the system power is on and this Power On/Off LED
is lit.
Color: Green

Powering the System
Power Off the System
To power off the system:

1. Lightly press the Power On/Off switch on top of the system
once. The Shutdown window is displayed.
NOTE: DO NOT press and hold down the Power On/Off switch to
shutdown the system. Instead, lightly press the Power On/
Off switch and select OK on the Shutdown window.
The shutdown process takes a few seconds.
NOTE: If the system does not fully shut down in 60 seconds, press
and hold down the On/Off switch until the system shuts
down.
2. Disconnect the probes.
Clean or disinfect all probes as necessary. Store them in
their shipping cases to avoid damage.
3. Disconnect AC power cord from the power outlet.
NOTE: Disconnect the AC adapter plug on the Docking Cart/Station
from the outlet to ensure the system is disconnected from
the power source.

Tilt LCD monitor

The LCD monitor position on the Docking Station/Cart can be
adjusted for easy viewing.
• Tilt the LCD monitor for the optimum viewing angle. The
maximum angle is 45 degrees.
Figure 2-30. LCD Monitor adjustment

Adjusting the Docking Cart

• To adjust the height of Docking Cart, hold the handle with
both hands, step on the pedal and adjust the height.
Figure 2-31. Adjust Docking Cart Height
CAUTION Be sure to lock the wheels before adjusting the Docking Cart
height.

Adjusting the Docking Cart (continued)
CAUTION When the cart handles are used for power cable management,
the sudden raising of the cart to a higher position may cause
the AC plug to break.
CAUTION When adjusting the cart while scanning, the power cord and
wheels may become entangled, which may result in cable
damage.
CAUTION Damage to the probe cable may result if the brake pedal
catches the cable and pulls it tightly against the base leg. This
puts stress on the probe and connector while the probe in the
probe holder.

Brightness
Adjusting the LCD monitor's brightness is one of the most
important factors for proper image quality.
To adjust the brightness:
1. Select Utility -> Settings -> Common, then choose the
desired brightness in the Brightness select box.
Figure 2-32. Brightness Adjustment
NOTE: The brightness of the LCD monitor’s Brightness should be set

first. Once set, this should not be changed unless the brightness
of your scanning environment changes.

Probes
Introduction
Only use approved probes.
All imaging probes can be connected into the probe port of the
Venue 50.
See ‘Probe Applications’ on page 5-20 for more information.
Selecting probes
• Always start out with a probe that provides optimum focal
depths and penetration for the patient size and exam.
• Begin the scan session using the default Power Output
setting for the probe and exam.

Probes
Connecting the Probe

Probes can be connected whether the console is powered on or
off. To ensure that the ports are not active, place the system in
the image freeze condition.
To connect a probe:
1. Place the probe's carrying case on a stable surface and
open the case.
2. Ensure the system is in freeze mode or powered off.
Carefully remove the probe and unwrap the probe cord.
3. DO NOT allow the probe head to hang free. Impact to the
probe head could result in irreparable damage.
Inspect the probe before and after each use for damage or
degradation to the housing, strain relief, lens, seal and
connector. DO NOT use a transducer which appears
damaged until functional and safe performance is verified. A
thorough inspection should be conducted during the
cleaning process.
4. Align the connector with the probe port and carefully push
into place.
Figure 2-33. Connect probe to Venue 50

Connecting the Probe (continued)

5. Carefully position the probe cord so it is free to move and is
not resting on the floor.
6. When the probe is connected, it is automatically activated.
CAUTION Fault conditions can result in electric shock hazard. Do not

touch the surface of probe connectors which are exposed
when the probe is removed. Do not touch the patient when
connecting or disconnecting a probe.
Cable Handling
Take the following precautions with probe cables:
• If the system in on the docking cart, please keep the probe
cable free from wheels and use the cable hooks on the
docking cart.
• DO NOT bend the cable acutely.
• Avoid crossing cables between probes.
Deactivating the Probe

When deactivating the probe, the probe is automatically placed
in standby mode.
To deactivate a probe:
1. Ensure the Venue 50 is in freeze mode or powered off.
2. Gently wipe the excess gel from the face of the probe.
3. Carefully slide the probe toward the probe holder on the
docking station. Ensure that the probe is placed gently in the
probe holder.

Probes
Disconnecting the Probe

1. Press to pop up the connector locking lever.
Figure 2-34. Pop up connector locking lever
2. Pull the probe and connector straight out of the probe port.
Figure 2-35. Disconnect probe from Venue 50
3. Carefully slide the probe and connector away from the

probe port.
4. Ensure the cable is free.
5. Be sure that the probe head is clean before placing the
probe in its storage box or a wall hanging unit.

Transporting Probes
Secure the probe in its holder for moving a short distance.
When transporting a probe for a long distance, store it in its
carrying case.
Storing the Probe

It is recommended that all probes be stored in the provided
carrying case or in the wall rack designed for probe storage.
1. First place the probe connector into the carrying case.
2. Carefully wind the cable into the carrying case.
3. Carefully place the probe head into the carrying case. DO
NOT use excessive force or impact the probe head.

Touch Panel
Touch Panel
You interact with Venue 50 using your fingers to tap, double-tap,

swipe, and pinch objects on the touch panel. Multi-touch with
fingers is supported by Venue 50.
Exam Function Controls

The touch panel contains exam function and mode/function
specific controls.
Figure 2-36. Venue 50 Menu Bar
1. Home: Enter home page 9. Split: Split the screen into two
2. Scan, Review: Perform various functions 10. Zoom: Magnify a region of interest
3. : eSmart Trainer (option) 11. Guide: Display the biopsy guidelines
4. Utility: Activate system configuration menus 12. End Exam: Press to end an exam
5. TGC, Gain, Depth: Adjust the image information 13. Dataflow Button: Store the patient information
6. B, Color, PDI, M: Switch to different modes or print the scanning images.
7. : configurable parameters 14. Freeze: Stop the acquisition of ultrasound
data and freeze the image in system memory.
8. Needle: Enhance visualization of the needle
CAUTION Use only fingers, or fingers with gloves to operate on the

system. Never use any sharp tools to scratch the LCD.

Monitor Display
Monitor Display
Figure 2-37. Monitor Display
1. Institution/Hospital Name, 7. MI, TI 13. Image area

Date, Time 8. Acoustic Output 14. Depth scale
2. Patient Name, Patient ID 9. Gain 15. Gray/Color bar
3. Storage device status 10. Center line mark 16. Measurement result window
4. Battery status 11. Measurement caliper 17. Cine Gauge
5. Wireless and local network 12. Comment 18. Function controls
connection status
6. Probe and application

Chapter 3
Performing an Exam
Describes how to perform an exam, annotate, measure

and store the images.

Performing an Exam
Performing an Exam
Overview
A typical exam includes the following:
• Begin a new exam
• Image scanning
• Measurements
• Annotations
• Image management

Begin a new exam
Begin a new exam
Introduction
Begin an exam by entering new patient information.
The operator should enter as much information as possible,
such as:
1. Patient Name
2. Patient ID
3. Study Description
4. Date of Birth (DOB)
5. LMP (if applicable)
6. Performing Physician
7. Patient Gender
The patient's name and ID number is retained with each
patient's image and transferred with each image during
archiving or hard copy printing.
CAUTION To avoid patient identification errors, always verify the

identification of the patient. Make sure the correct patient
identification appears on all screens and hard copy prints.

Performing an Exam
Beginning a New Patient
Tap Home to display the Home screen on the monitor.

Enter new patient information. Select the desired application.
Press Scan to begin the exam. At the end of each exam, all
patient data, annotations, measurements and images will be
stored in the patient files.
NOTE: The patient ID can be typed with the soft keyboard or
automatically created by pressing Auto.
NOTE: You can also scan without entering any patient data.See
‘Scanning without entering any patient data’ on page 3-7 for
more information.

Begin a new exam
Home Screen
Figure 3-1. Home Screen
1. Scan
2. Review
3. Utility
4. Patient Information
5. Preset Information
6. Clear
7. Soft Keyboard

Performing an Exam
Home Screen (continued)
The Home Screen details are:

1. Scan: To begin scanning.
2. Review: To review the desired patient from the archive.
3. Utility - To display the system configuration page.
4. Patient Information
• Patient Name–Last Name and First Name
NOTE: Only use periods, spaces, dashes and alphanumeric
characters for the Patient Name.
NOTE: The length of the Last Name and First Name should be
no longer than 16 characters.
NOTE: Patient information can be highlighted and edited with
fingers.
• Patient ID
Type the alphanumeric characters for the patient ID.
NOTE: Patient information cannot be saved without a patient
ID.
• 2nd ID
2nd ID is used to add additional information of the
patient, such as Citizen ID.
NOTE: To enable/disable 2nd ID field, go to Utility --> Settings
-> Common.
• Study Description: To describe the scanning area
• DOB: Date of Birth
• LMP: Last Menstrual Period. You may find LMP in
Obstetrics. Enter the date that the patient started her
last menstrual period. The format is the same as system
time format, which can be set in Utility -> General ->
Date and Time.
• Performing Phys: Physician who performs the study
• Gender: Male or Female
5. Preset Information: To choose the desired application.
6. Clear: To clear the patient information.
7. Soft Keyboard - To type text.

Begin a new exam
Scanning a New Patient
When starting a new patient’s exam, ensure you do the

following:
1. Press Home. The patient screen is displayed.
2. Fill in patient information by means of the following:
a. Fill in the patient information manually.
b. Press Worklist to select the desired patient from
worklist server and press Select or Select EM. The
patient information will show on the home screen.
c. If the last patient exam does not end, press New
Patient and fill in the patient information manually.
3. Select the application from Preset Information (if not
automatically selected).
4. Press Scan to perform the exam.
5. Store data to patient files.
You may choose more applications for the same patient by
tapping Home-> Preset Information in live scanning mode.
Scanning without entering any patient data
To scan a patient without entering any patient data:

1. Press Scan to perform the exam and save images/videos.
2. Patient images/videos are stored in the storage device, refer
to ‘Image Storage’ on page 3-88.

Performing an Exam
Image Scanning
B Mode
Intended Use
B Mode is intended to provide two-dimensional images and

measurement capabilities concerning the anatomical structure
of soft tissue.

Image Scanning
B Mode Controls
Figure 3-2. B Mode Controls
Table 3-1: B Mode Controls
Controls Affect on Image
TGC Adjust TGC to balance the image so that the density of echoes is the same
throughout the image.
Gain Makes images brighter or darker.
Depth Press to increase or decrease scanning depth.
B/Color/PDI/M Switch to PDI/Color Flow/M mode, different option for different packages.
Press left or right justification pointer to show more image area.

Note: The justification pointers are available only when the scanning depth is equal
to or less than 1cm.
Note: The justification pointers are only available for linear probes.

Performing an Exam
Table 3-1: B Mode Controls
Needle
Press to activate the Needle mode. Gain, Angle and Tilt can be activated.
The needle function only applies to linear probes.
Caution: Before activating the Needle, please make sure to select Interventional
related preset first.
Split Press to split the screen into two.
Zoom Press to magnify the region of interest.
Guide Press to display the biopsy guidelines.
Configurable • LiveGain: To balance echo contrast so that cystic structures appear echo-free and
Parameters reflecting tissue fills in.
• Frequency: This optimizes the probe’s wide band imaging capabilities at multiple
frequencies to image at greater depths.
• CrossXBeam: Improve contrast resolution with increased conspicuity of low
contrast lesions, better detection of calcifications, biopsy needle visualization, and
cystic boundary definition.
• Gray Map: Affects the presentation of B Mode information.
• Focus Pos: Focus optimizes the image by increasing the resolution for a specific
area.
• Reverse: Used for anatomical correctness.
• ATO Level: Select the Auto Tissue Optimize Level to pick a preference for the
contrast enhancement in the resulting image.
• Dynamic Range: It is useful for optimizing tissue texture for different anatomy.
• Compression: Suppress the noise in the image.
• Rejection: Allow for the elimination from the display of low level echoes caused by
noise.
• Frame Aver: Smooth the image.
• SRI HD: Smooth the image when image speckle interferes with the desired image
detail
• Edge Enhance: Make the image edge clearer/sharper.
• FOV: Adjust field of view
• AO: Adjust acoustic output
Note: The configurable parameters can be configured in Utility -> Settings -> ScanConfig.

Image Scanning
Color Flow Mode
Intended Use
Color Flow Mode is a Doppler Mode intended to add

color-coded qualitative information concerning the relative
velocity and direction of fluid motion within the B-Mode image.

Performing an Exam
Color Flow Mode Controls
Figure 3-3. CF Mode Controls
Table 3-2: CF Mode Controls
ROI Use two fingers to adjust the size of the ROI. Or press the ROI and move it to the
desired position.
Hold the pointer and move left or right to adjust the angle of the ROI.
Note: The justification pointers are available only when the scanning depth is equal
to or less than 1cm.
Note: The justification pointers are only available for linear probes.

Image Scanning
Table 3-2: CF Mode Controls
Configurable • Scale: Imaging of higher velocity flow requires increased scale values to avoid
Parameters aliasing.
• Threshold: Limit color flow overlay to low level echoes inside vessel walls. Help to
minimize color ‘bleeding’ outside vessel walls.
• Sample Vol: Place the sample volume gate to sample blood flow.
• Steer: Provide a doppler cursor angle suitable for linear probe orientation.
• Wall Filter: Decrease, unnecessary low frequency signals caused by motion.
• Color Map: Show the direction of the flow and highlight the higher velocity flows.
• Invert: Allow to view blood flow according to personal preference, without flipping
the probe.
See Table 3-1 for more information.

Performing an Exam
Power Doppler Imaging (PDI)
Intended Use
Power Doppler Imaging (PDI) is a color flow mapping technique

used to map the strength of the Doppler signal coming from the
flow rather than the frequency shift of the signal.

Image Scanning
PDI Mode Controls
Figure 3-4. PDI Mode Controls
Table 3-3: PDI Mode Controls
Configurable • PDI Map: Show the power of the flow and highlight the stronger power flows.
Parameters
See Table 3-1 and Table 3-2 for more information.

Performing an Exam
M Mode
Intended Use
M Mode is intended to provide a display format and

measurement capability that represents tissue displacement
(motion) occurring over time along a single vector.

Image Scanning
M Mode Controls
Figure 3-5. M Mode Controls
Table 3-4: M Mode Controls
Configurable • Sweep Speed: Change the speed of the timeline.

Parameters • Layout: Change the Horizontal/Vertical layout between B Mode and M Mode.
See Table 3-1 for more information.

Performing an Exam
Measurements
Introduction
Measurements derived from ultrasound images are intended to
supplement other clinical procedures available to the attending
physician. The accuracy of measurements is not only
determined by system accuracy, but also by the use of proper
medical protocols by the operator. When appropriate, be sure to
note any protocols associated with a particular measurement or
calculation. Formulas and databases used within the system
software that are associated with specific investigators are so
noted. Be sure to refer to the original article describing the
investigator's recommended clinical procedures.

Measurements
B Mode Measurements
Below measurements can be made in B-Mode.
• Distance
• Ellipse
• Volume
• Trace
• Open Trace
• Angle
NOTE: The following instructions assume that you first scan the patient
and then press Freeze.
Figure 3-6. Frozen Mode
NOTE: Only 5 measurements are allowed at the same time.

Performing an Exam
Distance Measurement
To make a distance measurement:

1. Press Measure.
Figure 3-7. Measure Screen
2. Select Distance.
Figure 3-8. Distance Screen
3. Touch the screen, and two active calipers display.

4. Move the calipers to the desired position.

Measurements
Distance Measurement (continued)
5. Press Set.
The system displays the value in the Results Window.
Figure 3-9. Distance Measurement
NOTE: If you touch the very edge of the scanning screen, the
calipers will display at the center of the screen. You may
move the calipers to the desired position to do the
measurement.

Performing an Exam
Ellipse Measurement
You can use an ellipse to measure circumference and area. To

measure with an ellipse:
1. Press Measure, then select Ellipse.
Figure 3-10. Ellipse Screen
2. Touch the screen, and three active calipers display.

4. Press Set.
Figure 3-11. Ellipse Measurement

Measurements
Volume Measurement
To make a volume measurement:

1. Press Measure, then select Volume.
Figure 3-12. Volume Screen

4. Press Set and the first distance value appears in the Results
Window.
5. Repeat Step 1-4 twice and the system displays the volume
value in the Results Window.
Figure 3-13. Volume Measurement

Performing an Exam
Trace Measurement
To trace the circumference of a portion of the anatomy and

calculate this area:
1. Press Measure, then select Trace.
Figure 3-14. Trace Screen
2. Touch the screen, and an active caliper displays.

3. Move the caliper to the start position and press Set to fix the
trace start point.
4. Move the caliper around the anatomy. A dotted line shows
the traced area.
5. Press Set.
Figure 3-15. Trace Measurement

Measurements
Open Trace Measurement
To trace and calculate the circumference of a portion of the

anatomy:
1. Press Measure, then select Open Trace.
Figure 3-16. Trace Screen
2. Touch the screen, and an active caliper displays.

3. Move the caliper to the start position and press Set to fix the
trace start point.
4. Move the caliper around the anatomy. A dotted line shows
the traced area.
5. Press Set.
Figure 3-17. Open Trace Measurement

Performing an Exam
Angle Measurement
This function measures the angle between two intersecting

planes:
1. Press Measure, then select Angle.
Figure 3-18. Angle Screen

4. Press Set.
Figure 3-19. Angle Measurement

Measurements
M Mode Measurements
Basic measurements that can be taken in the M Mode portion of
the display are:
• Depth
• Heart Rate
NOTE: The following instructions assume that you do the following:
1. In B Mode, scan the desired anatomy you wish to measure.
2. Go to the M Mode part of the display.
3. Press Freeze.

Performing an Exam
Depth
To make a distance measurement:

1. Press Measure, then select Depth.
Figure 3-20. Depth Screen

4. Press Set.
Figure 3-21. Depth Measurement

Measurements
Heart Rate
To measure time and velocity between two points:

1. Press Measure, then select Heart Rate.
Figure 3-22. Heart Rate Screen

4. Press Set.
Figure 3-23. Heart Rate Measurement

Performing an Exam
Measurement Controls
Figure 3-24. Measurement controls
Table 3-5: Measurement Controls
Set Set measurements
Select Select the desired measurements
Delete Delete the selected measurements
Delete All Delete all measurements
Exit Exit the measurement window
Undo Undo the trace measurement bit by bit. (It is only applied for Trace and Open Trace
measurement.)
Note: Press Select for one time to select the first measurement; Press Select for the second time to select
the second measurement, and so on.

Measurements
Obstetrics Measurements
The following pages describe how to make OB measurements.
Out of Range - If the system indicates that a measurement is out
of range (OOR), it means one of the following:
• The measurement is out of the normal range based on the
gestational age that is calculated from the LMP. The system
determines OOR from the ultrasound age compared to the
gestational age. The gestational age is calculated from the
last menstrual period.
• The measurement is outside of the range for the data used
in the calculation. That means that the measurement is
either less than or more than the range of measurements
used to determine fetal age based on the measurement.
NOTE: Calculation formulas are listed in the Advanced Reference
Manual.
NOTE: The Obstetrics measurements can be configured in Utility ->
Measure -> Measure.
NOTE: Operators may choose different measurement types based on
their regional preferences.
WARNING The system provides calculations (e.g estimated fetal weight)

and charts based on published scientific literature. The
selection of the appropriate chart and clinical interpretation of
calculations and charts is the sole responsibility of the operator.
The operator must consider contraindications for the use of a
calculation or chart as described in the scientific literature. The
diagnosis, decision for further examinations and medical
treatment must be performed by qualified personnel following
good clinical practice.
NOTE: The following instructions assume that you first go to Home ->
Preset Information -> OB1/OB2/3, press Scan and then
Freeze.
NOTE: Only 5 measurements are allowed at the same time.

Performing an Exam
Gestational Sac (GS)

To calculate the gestational sac, make one or three distance
measurements.
GS(1 Caliper)
To make a GS(1 Caliper) measurement:

1. Press Measure, then select GS (1 Caliper).
Figure 3-25. GS (1 Caliper) Screen

4. Press Set.
Figure 3-26. GS (1 Caliper) Measurement

Measurements
GS(3 Calipers)
To make a GS(3 Calipers) measurement:

1. Press Measure, then select GS (3 Calipers).
Figure 3-27. GS (3 Calipers) Screen

Window.
5. Repeat Step 1-4 twice and the system displays the GS
value in the Results Window.
Figure 3-28. GS (3 Calipers) Measurement

Performing an Exam
Crown Rump Length (CRL)

To measure crown rump length, make one distance
measurement:
1. Press Measure, then select CRL.
Figure 3-29. CRL Screen

4. Press Set.
Figure 3-30. CRL Measurement

Measurements
Biparietal Diameter (BPD)

To measure biparietal diameter, make one distance
measurement:
1. Press Measure, then select BPD.
Figure 3-31. BPD Screen

4. Press Set.
Figure 3-32. BPD Measurement

Performing an Exam
Abdominal Circumference (AC)

To measure abdominal circumference, make a diameter
measurement.
1. Press Measure, then select AC (Diameter).
Figure 3-33. AC (Diameter) Screen

4. Press Set to get the first diameter.
5. Repeat Step 1-4 to get the second diameter.
Figure 3-34. AC (Diameter) Measurement

Measurements
Abdominal Circumference (AC) (continued)

To measure abdominal circumference, make an ellipse
measurement.
1. Press Measure, then select AC (Ellipse).
Figure 3-35. AC (Ellipse) Screen

4. Press Set.
Figure 3-36. AC (Ellipse) Measurement

Performing an Exam
Femur Length (FL)

To measure femur length, make one distance measurement:
1. Press Measure, then select FL.
Figure 3-37. FL Screen

4. Press Set.
Figure 3-38. FL Measurement

Measurements
Antero-Postero Trunk Diameter by Transverse Trunk Diameter (AxT)

Make two distance measurements, one of the antero-postero
trunk diameter and one of the transverse trunk diameter.
1. Press Measure, then select AxT.
Figure 3-39. AxT Screen
2. Make a distance measurement of the antero-postero trunk

diameter (APTD).
a. Touch the screen, and two active calipers display.
b. Move the calipers to the desired position.
c. Press Set.
The system displays the distance value in the Results
Window.
3. Make a distance measurement of the transverse trunk
diameter (TTD), repeat steps a-c above.
The system displays the AxT value in the Results Window.
Figure 3-40. AxT Measurement

Performing an Exam
Spine Length (SL)

To measure spine length, make one distance measurement:
1. Press Measure, then select SL.
Figure 3-41. SL Screen

4. Press Set.
Figure 3-42. SL Measurement

Measurements
Cardio-Thoracic Area Ratio (CTAR)

To calculate cardio-thoracic area ratio, you make two ellipse
measurements.
1. Press Measure, then select CTAR.
Figure 3-43. CTAR Screen
2. Make an ellipse measurement of the cardiac area.

a. Touch the screen, and three active calipers display.
b. Move the calipers to the desired position.
c. Press Set.
The system displays the cardiac area value in the
Results Window.
3. Make an ellipse measurement of the thoracic area, repeat
step a-c above.
The system displays the CTAR value in the Results Window.
Figure 3-44. CTAR Measurement

Performing an Exam
Amniotic Fluid Index (AFI)

To calculate the amniotic fluid index, make one or four distance
measurements.
AFI(1 Caliper)
To make a AFI (1 Caliper) measurement:

1. Press Measure, then select AFI (1 Caliper).
Figure 3-45. AFI (1 Caliper) Screen

4. Press Set.
Figure 3-46. AFI (1 Caliper) Measurement

Measurements
AFI(4 Calipers)
To make a AFI(4 Calipers) measurement:

1. Press Measure, then select AFI (4 Calipers).
Figure 3-47. AFI (4 Calipers) Screen

Window.
5. Repeat Step 1-4 three times and the system displays the
AFI value in the Results Window.
Figure 3-48. AFI (4 Calipers) Measurement

Performing an Exam
Cervical Length (CL)

To measure cervical length, make one distance measurement:
1. Press Measure, then select CL.
Figure 3-49. CL Screen

4. Press Set.
Figure 3-50. CL Measurement

Measurements
Humerus Length (HL)

To measure humerus length, make one distance measurement:
1. Press Measure, then select HL.
Figure 3-51. HL Screen

4. Press Set.
Figure 3-52. HL Measurement

Performing an Exam
Head Circumference (HC)

To make a HC (Hadlock) - Diameter measurement:
1. Press Measure, then select HC (Diameter).
Figure 3-53. HC (Diameter) Screen

4. Press Set to get the first diameter.
5. Repeat Step 1-4 to get the second diameter.
Figure 3-54. HC (Diameter) Measurement

Measurements
Head Circumference (HC) (continued)

To make a HC (Hadlock) - Ellipse measurement:
1. Press Measure, then select HC (Ellipse).
Figure 3-55. HC (Ellipse) Screen

4. Press Set.
Figure 3-56. HC (Ellipse) Measurement

Performing an Exam
Fetal Trunk Cross-Sectional Area (FTA)

To measure fetal trunk cross-sectional area, make an ellipse
measurement.
1. Press Measure, then select FTA.
Figure 3-57. FTA Screen

4. Press Set.
Figure 3-58. FTA Measurement

Measurements
Estimated Fetal Weight (EFW)

To measure estimated fetal weight, you make several OB
measurements. These measurements can vary, based on how
your system is set up. Measurements can include biparietal
diameter, fetal trunk area, femur length, antero-postero trunk
diameter and transverse trunk diameter, abdominal
circumference, head circumference and spinal length.
The system displays each measurement and the estimated fetal
weight in the OB Worksheet.
NOTE: For a description of any of the required measurements, refer to
that measurement.
NOTE: The EFW can be configured in Utility -> Measure ->
Obstetrics.

Performing an Exam
Annotations
Introduction
Select Comment to activate comment mode.
The comment function provides the capability to type the
comments of free text and/or add the comments from the
comment library. It also provides the operator with bodymark
and arrow pointers.
NOTE: Annotations are only available in frozen mode.
NOTE: The following instructions assume that you first scan the patient
and then press Freeze.
Comment Retention
Comments will be retained and carried over when switching to
multi-image mode.
The position of the comments is adjusted so that it is at the
same relative position with respect to the display window in the
new format as it was in the single image format.

Annotations
Annotating an image using the library
Annotating an image using the system preset library
1. Press Comment, then press Annotation.

2. Choose the desired comment from the system preset library.
NOTE: You may swipe the screen to see more comments in the
preset library.
3. Move the annotation box to the desired position. Press
anywhere on the scanning screen to set the comment or
select to clear the comment.
Figure 3-59. Preset Library

Performing an Exam
Annotating an image using the customer defined library
Creating/Editing comments for customer defined library

To create or edit comments for customer defined library:
1. Press Comment, then press Custom.
2. Select .
Figure 3-60. Customer Defined Library

Annotations
Creating/Editing comments for customer defined library (continued)

3. Select a blank tab to create a new comment or select a
defined tab to edit the comment, then press Save to save
the new or edited comments.
4. Select Exit to exit comments defined screen.

Performing an Exam
Annotating an image using the customer defined library

1. Press Comment, then press Custom.
2. Choose the desired comment from the customer defined
library.

Annotations
Annotating an image with typed words

1. Press Comment.
2. Press Keyboard, then type comments.
Figure 3-63. Keyboard

Performing an Exam
Bodymark
1. Press Bodymark.
2. Select the desired bodymark and move it to the desired
position on the screen.
3. Press anywhere on the scanning screen to set the
bodymark or press to delete it.
Figure 3-64. Bodymark

Annotations
Arrow Pointers
1. Press Comment, then select Arrow.
2. Select the desired arrow pointer and move it to the target
position on the screen.
NOTE: You may change the size of the arrow pointers by selecting
Small, Medium or Large.
3. Press anywhere on the scanning screen to set the arrow
pointer or press to delete it.
Figure 3-65. Arrow

Performing an Exam
Edit while annotating

There are two modes of comments available: Active and
Confirm. The comments are green while active and yellow when
set.
NOTE: Comments can only be edited in the active mode.
To delete the annotation
1. Press Freeze.
2. Select Comment.
3. Select the desired comment and press to delete it.
4. To delete all the comments, select Delete All.
NOTE: If you select Delete All, all comments, including arrow pointers,
bodymarks and text, will be deleted.
To move the annotation
1. Press Freeze.
2. Select Comment.
3. Select the desired comment and move it to the target
position.
Annotation Controls
Figure 3-66. Annotation mode controls
Table 3-6: Annotation controls
Controls Affects on image
Annotation Select the comments from the preset library.
Keyboard Type the comments with alphabets.
Custom Create or edit for customer defined library.
Arrow Select for arrow placement.
Delete All Delete all annotations.
Exit Exit the annotation screen.

OB Worksheet
OB Worksheet
OB Worksheet summarizes the data obtained in the

examination. They can contain data, images, and cine loops.
Once generated, the worksheet can be viewed, images can be
added, and the patient’s personal data can be modified. The
examination data itself CANNOT be changed.
NOTE: OB Worksheet function is only available when the OB package
option is activated.

Performing an Exam
Activating the Worksheet

Select Worksheet in frozen mode.
Figure 3-67. Worksheet

OB Worksheet
OB Worksheet Controls
Figure 3-68. OB Worksheet Controls
Table 3-7: OB Worksheet Controls
Controls Function Description
Report Press to view the report sheet.
Clear Press to clear the all the information in OB Worksheet except Patient ID, Name and
Age.
Reset Press to reset the worksheet.
Store to Press to set store destination.
Store Press to store the worksheet.
Print Press to print the worksheet.

Performing an Exam
OB Worksheet information
OB Worksheet information:
Figure 3-69. OB Worksheet page - page1
1. Patient information
Table 3-8: Patient information
Field Description
ID, Name, Age Patient ID, Patient name and patient age.
LMP Last Menstrual Period; the LMP can be entered and edited in the patient screen.
EDD(LMP) Estimated Delivery Date by LMP; the system fills in the date after you enter the LMP.
GA(LMP) Gestational Age by LMP; the system fills in the age after you enter the LMP.
EDD(CUA)/ Estimated Delivery Date by CUA/AUA.

EDD(AUA)
CUA/AUA Select the ultrasound age calculation method in this field.

CUA: Composite Ultrasound Age, regression calculation;
AUA: Average Ultrasound Age, an arithmetic average.

OB Worksheet
Table 3-8: Patient information
Field Description
Fetus# Number of fetuses; default is 1. Can be 1, 2 or 3.
A/B/C The first/second/third fetus.
2. 2D Measurements information
Table 3-9: 2D Measurements information
Field Description
Parameter Measurement name
CUA/AUA If this field is checked, the system uses the measurement to calculate the ultrasound
age.
Value The measured value. If more than one measurement was made for an item, the
system uses the specified method (average, last) to determine this value. Average for
USA and Europe; Last for Osaka, Tokyo and ASUM.
m1, m2 Up to two measurement values for each item. If you make more than two
measurements, the system uses the last two.
Method When there is more than one measurement for an item, this specifies the method
used to calculate the measurement value listed in the Value column. Average for USA
and Europe; Last for Osaka, Tokyo and ASUM.
GA Gestational Age.
GA Range/GP/SD The typical range of gestational age/growth percentile/standard deviation for this
measurement.

Performing an Exam
OB Worksheet information (continued)
3. OB Calculation
Table 3-10: OB Calculation information
Field Description
EFW Estimated fetal weight; lists the parameters used to calculate EFW. This is followed by
the calculation result.
NOTE: EFW can be configured in Utility->Measure->Obstetrics.
EFW-GP Lists the source used to calculate EFW-GP (growth percentile). This is followed by the
growth percentile.
CI Cephalic Index.
FL/AC, FL/HC, Ratios for the measurements

FL/BPD, HC/AC
AFI Amniotic Fluid Index.

OB Worksheet

4. MM Measurement
Table 3-11: MM Measurements information
Field Description
Parameter Measurement name
Value The measured value. If more than one measurement was made for an item, the
system uses the specified method (average, last) to determine this value. AVG for
USA and Europe; LAST for Osaka, Tokyo and ASUM.
m1, m2 Up to two measurement values for each item. If you make more than two
measurements, the system uses the last two.
Method When there is more than one measurement for an item, this specifies the method
used to calculate the measurement value listed in the Value column. Choices are
AVG, MAX, MIN or LAST.

Performing an Exam
5. Measurement Type
NOTE: You may choose the measurement type from the pull-down
list and the screen will show the corresponding figure.

OB Worksheet
6. Report Image
7. Patient Image
NOTE: The Patient Image here does not include worksheet images.

Performing an Exam
8. BIO-PHYSICAL PROFILE
Table 3-12: Measurements information
Field Description
BIO-PHYSICAL The score is _ of 10 possible total points, depending upon the number of parameters
PROFILE entered. Enter the following information to assess the fetus’s biophysical well-being.
Movement Type 0, 2 or *
Tone Type 0, 2 or *
Breathing Type 0, 2 or *
Fluid Type 0, 2 or *
Reactive NST Type 0, 2 or *

OB Worksheet

9. Summary and Physician
Table 3-13: Summary and physician information
Field Description
Summary Free text, the characters should be less than 300.
Physician Physician

Performing an Exam
Editing OB Worksheet
Editing the patient information
The CUA/AUA and fetus # can be edited.
Editing measurements
The CUA/AUA, m1, m2 and method and can be edited.
Editing calculation
The AFI can be edited.
Editing the report Image
Double click the desired image in the patient image area to copy
the image to the report image area.
Double click the image again to delete the image from the report
image area.
Editing the Bio-physical profile
The Movement, Tone, Breathing, Fluid and Reactive NST can

be edited.
Editing summary and Physician by
The summary and physician can be edited.

OB Worksheet
OB Report
Select Report on the OB worksheet page, then the report will be
shown on the screen.
Figure 3-74. OB Report page

Performing an Exam
OB Report controls
Worksheet
Press to exit the OB report page and return to the OB worksheet
page.
Store To
Press to set the store destination.
Store
Press to store the OB Report.
Save Text
Press to save the OB report in text format to the patient folder.
Save PDF
Press to save the OB report in PDF format to the patient folder.
Print
Press to print the OB report. Only the information above the
images will be printed.

OB Worksheet
Multi gestational
Venue 50 allows you to measure and report multiple fetus
development. The system can report a maximum of three
fetuses.
To enter the number of fetuses
If more than one fetus is imaged during the exam, enter the
number of fetuses in the OB worksheet page.
When you start OB exam, the system automatically defaults to
Fetus #1, it can be changed to Fetus #2 or Fetus #3.
To identify each fetus
For measurements, calculations, and worksheet displays, the

system labels each fetus A, B or C.
To select a fetus
During measurements, to change between fetuses:

Select the desired fetus in OB worksheet page.
NOTE: After you change to the next fetus, any measurements you
make are recorded and reported to that fetus. If you have any
active measurement that is not completed when you change the
fetus, the system cancels the measurement.
To view multiple fetuses
Multiple gestation data is displayed on the OB report and graph.

Performing an Exam
Storing an OB Report
The OB Report can be stored in JPEG, Text or PDF format.
To Store an OB Report:
1. Select Report on the OB worksheet page to enter into OB
report page.
2. Press Store To to set the store destination.
Figure 3-75. Set Store Destination
3. Press Store to save the OB report in JPEG format to the

patient folder.
4. Press Save Text or Save PDF to save the OB report in text
format or in PDF format to the patient folder.

Image Management
Image Management
Zooming an Image
Introduction
Zoom is used to magnify a region of interest (ROI). The system

adjusts all imaging parameters accordingly. You can zoom a live
or frozen image with your fingers.
Bioeffect
Zooming an image changes the frame rate which tends to

change thermal indices. The position of the focal zones may
also change which may cause the peak intensity to occur at a
different location in the acoustic field. As a result, the MI (TI)
may change.
Acoustic Observe the output display for possible effects.

Output
Hazard
To zoom an image, press Zoom. A reference image appears in

the lower, right-hand section of the display. You may use your
fingers to zoom the image.
To exit zoom, press Zoom or press B Mode if in Live scan
mode.

Performing an Exam
Split Screen
Overview
To activate split screen, press Split.

• In live mode
When you press Split, both the latest frame that the system
automatically stored and the live image will be on the
screen.
• In frozen mode
When you press Split, both the latest image that you stored
and the live image will be on the screen.
To exit split, press Split or press B Mode.

Image Management
Using Cine
Introduction
Cine is useful for focusing on images during a specific part of the

cycle or to view short segments of a scan session.
You can view Cine as a continuous loop via Cine Loop or
manually review Cine images frame by frame.
Data in Cine is available until new data is acquired. Cine can be
archived in the storage device.

Performing an Exam
Activating Cine
To activate Cine,
1. Press Freeze
Figure 3-76. Cine screen

Image Management
Cine controls
Figure 3-77. Cine controls
Table 3-14: Cine controls
Controls Affects on images
< View previous frame
> View next frame
Play/Pause Playback/Pause the Cine loop
NOTE: Use the fingers to select the processing bar to view frames.

Performing an Exam
Review Archived Information
Searching for an existing patient
1. Select Review, then the patient gallery under the storage

device displays on the screen.
Figure 3-78. Gallery Screen

Image Management
Searching for an existing patient (continued)
2. Enter Patient ID or Name, then select the desired patient.
Figure 3-79. Patient Search screen
3. The patient information displays on the screen.

Performing an Exam
Editing patient information
To edit patient information,

1. Press Review, then select the desired patient from the
patient gallery.
2. Press Update to edit the patient information.
Figure 3-80. Patient Edit page
a. If the patient is an emergency one (i.e. without entering

any information before scanning), the operator can edit
all the patient information, including patient ID.
NOTE: The patient ID can be revised only once.
b. If the patient is not an emergency patient, the operator
can edit all the patient information, excluding the patient
ID.

Image Management
Editing patient information (continued)
If the patient is an emergency patient, you may follow the

way to edit patient information as above, or you may do as
follows:
1. After the exam, press Home -> Manual -> Update
Demographic to edit the patient information.
Figure 3-81. Emergency patient edit page
2. Press Scan to begin an exam or end an exam. The updated

patient information will be stored.

Performing an Exam
Reviewing the patient exam
To review the patient exam,

1. Press Review, then select the desired patient from the
Archive.
The images/videos of the selected patient are displayed at
the bottom of the screen. You may swipe left or right to see
more images/videos.
Figure 3-82. Review patient exam

Image Management
Reviewing the patient exam (continued)
2. Tap the desired image or video, press Review and it will be

displayed on the review screen.
Figure 3-83. Review Patient Exams
3. In the review screen, press Split to split the scanning

screen. Press Print to print the image. Press Delete to
delete the image or video. Press Close to exit to the patient
gallery.
Figure 3-84. Review Screen

Performing an Exam
Deleting the existing patient/images
CAUTION Before deleting a patient or image from the Patient Screen,

make sure you have already saved the patient data. GE is not
responsible for any patient information loss.
Deleting the existing patient

1. Search and select the patient in the patient list.
2. Press Delete. The confirmation dialog box displays.
Figure 3-85. Delete Patient
3. Select OK to delete or select Cancel to exit.

Image Management
Deleting the existing image/video

1. Select the patient in the patient list.
2. Press the desired image.
3. Press Delete. A dialog box displays. Select OK to delete or
select Cancel to exit.
Figure 3-86. Delete Image/Video

Performing an Exam
Image Storage
Storing an image
Images can be stored in JPEG format.

To store an image in frozen mode:
1. While scanning, press Freeze.
2. Scroll through the Cine Loop and select the desired image.
3. Press the appropriate Dataflow Button to save the image.
To store an image in live scan mode:
1. Go to Utility -> Settings -> Common, then choose Image
in Live Scan Save.
2. Select Save, then select Exit to enter into scan screen.
3. While scanning press Dataflow Button to save the image.
A message “Image saved successfully“ displays on the
screen.
Figure 3-87. Image Saved

Image Management
Storing a Video clip
Video clips can be stored in MPEG format.

A Cine Loop is a sequence of images recorded over a certain
timeframe.
1. Go to Utility -> Settings -> Common, then choose Video in
Live Scan Save.
2. Select Save, then select Exit to enter into scan screen.
3. While scanning or playing back a cineloop, press the
Dataflow Button to save the video.
4. A processing box showing storing progress displays.
5. A message “Video saved successfully“ displays on the
screen.
WARNING Imaging functions may be lost without warning. Develop

emergency procedures to prepare for such an occurrence.
CAUTION Do not cut off system power supply during image/video storing
process.

Performing an Exam
Storage device status
View storage device status

After the selected storage device is detected by the system,
there is an icon on the screen.
Figure 3-88. Storage device status icon
When the storage device is full

When the storage device is almost full, the following icon
displays:
Figure 3-89. Storage device is almost full
When storing images, videos or saving patient, a warning

message:” Storage space is almost full, saving image/video/
patient failed” displays.
NOTE: Please change the storage device at once and save images/
videos again.
When the storage device is not available

If the selected storage device is not available, the following icon
displays:
Figure 3-90. Storage device is not available by system
NOTE: Make sure the selected storage device is functioning properly, or

please check it in Utility. Please refer to Chapter 4 for detailed
information.
NOTE: Make sure the selected storage device is connected properly.

Image Management
View images/videos on PC
To view archived images/videos on a PC,

NOTE: It is recommended to view videos by QuickTime. If you do not
have QuickTime on your PC, you can download it free from
www.apple.com.
1. Tap the storage device status icon, press “Eject SD” or
“Eject USB”, then remove the storage device from the
system.
CAUTION DO NOT disconnect the SD Card or USB Memory Stick

from Venue 50 without properly ejecting the device; this
may result in loss of data.
2. Connect the storage device to the PC.

• For USB Memory Stick, connect to the USB port of a
PC.
• For High Capacity SD Card, insert it to SD Card Reader
and connect to the USB port of a PC.
3. Find the patient images and videos in the patient folder.
• PatientID@_@_LastName@_FirstName@_UserName@
_StudyDate.
• For those registering with Patient ID and 2nd ID, the
folder name is
PatientID@_2ndID@_LastName@_FirstName@_User
Name@_StudyDate.
• For those registering with auto Patient ID, the folder
name is AutoID@_@_@_@_UserName@_StudyDate.
• For those scanning without patient registration, the
folder name is
EAutoID@_@_@_@_UserName@_StudyDate.
NOTE: In case of emergency, you can scan without entering
patient information. In these cases, the system
automatically generates the ID.
4. View patient images and videos on a PC.

Performing an Exam
Connectivity
Overview
You can set up the connection and communication protocols for
the ultrasound system. This page gives an overview of each of
the connectivity functions.
To set up your institution’s connectivity, you must login with
administrative privileges.
1. DICOM Worklist: Search and Retrieve Patient Information
2. DICOM Image Store: Transfer DICOM images or videos to
DICOM image server.
3. Network QuickSave: Transfer images and CINE loops to
network shared folder.

Image Management
Network Status
View network status

There are two icons indicating wired and wireless network
status.
The following icons indicate that the wired and wireless network
are connected:
Figure 3-91. Wired network status icon - connected
Figure 3-92. Wireless network status icon - connected
When the network is disconnected

The following icons indicate that the wired and wireless network
are disconnected:
Figure 3-93. Wired network status icon - disconnected
Figure 3-94. Wireless network status icon - disconnected
When the wireless network is limited

The following icons indicate that the wireless network is limited
or no connection is available:
Figure 3-95. Wireless network status icon - limited or no

connection available

Performing an Exam
DICOM Worklist
1. Select Home, then select Worklist. The patient list used
last time displays.
Figure 3-96. Patient list in worklist server
NOTE: The worklist server can be configured in Utility, refer to

Chapter 4.

Image Management
DICOM Worklist (continued)

2. Press Refresh, the patient list which meets the search
criteria in the worklist server displays.
NOTE: The Search Criteria may be configured in Utility ->
Connectivity -> DICOM.
3. Select the desired patient, press Select EM or Select, the
patient information is automatically populated.
Or
Enter Patient ID, Patient Name, Accession, Modality and/or
Date to search the patient. Press Select, the patient
information is automatically populated.
NOTE: Only when the patient is an emergency one, can the
operator press Select EM.
Figure 3-97. Search patient list in worklist server
4. Press Scan to begin an exam.

Performing an Exam
DICOM Image Store

DICOM Image Store allows the system to send ultrasound
images in a format that can be interpreted by PACS.
NOTE: All still images can be sent to DICOM image server.
NOTE: Video may be sent to DICOM image server only if Enable
MultiFrame DICOM is selected.
NOTE: The multiframe video is limited to 3 seconds.
NOTE: The DICOM image server can be configured in Utility, refer to
Chapter 4.
1. Select Review. The patient gallery displays on the screen.
2. Select the desired image or video, select (PACS) in the
lower right corner. The image or video will be sent to the
DICOM image server.
Figure 3-98. DICOM image/video

Image Management
DICOM Image Store (continued)

Or
Select the desired patient, select (PACS) on the right
side. The images and videos of the patient will be sent to the
DICOM image server.
Figure 3-99. DICOM patient data
NOTE: The transfer status can be viewed in Spool, refer to ‘Spool’

on page 3-100.

Performing an Exam
Network QuickSave
Network QuickSave allows the system to send ultrasound
images in JPEG format and CINE loops in MPEG format.
NOTE: The network shared folders can be configured in Utility, refer to
Chapter 4.
1. Select Review. The patient gallery displays on the screen.
2. Select the desired image or Cine loop, select in the
lower right corner. The image or Cine loop will be sent to the
Figure 3-100. Network image/video

Image Management
Network QuickSave (continued)

Or
Select the desired patient, select on the right side. The
images and Cine loops of the patient will be sent to the
Figure 3-101. Network patient data

Performing an Exam
Spool
To monitor/control DICOM jobs, select Review -> Spool. You
can view, refresh, resend, and delete images from DICOM spool
by selecting a job, then specifying the action to be performed on
this job.
NOTE: If you find a failed job(s) in the Spool, please remove the failed
job(s) from the Spool.
Figure 3-102. Example screen of Spool
Table 3-15: Job status
Status Description
Ready The image transfer is ready.
Start The image transfer has started.
Finished The image transfer is successfully finished.
Failed Unsuccessful job attempt. Job stays in spool. Select Resend or Delete to
complete the job.

Image Management
eSmart Trainer (Option)

The system provides eSmart Trainer function.
To activate the eSmart Trainer function:
1. Go to Utility -> Settings -> Config Page, then activate the
eSmart Trainer function. Press Save.
Figure 3-103. Activate eSmart Trainer

Performing an Exam
eSmart Trainer (Option) (continued)

2. Press Utility -> Settings -> Miscellaneous to choose the
desired trainer setting. Press Save.
Figure 3-104. Trainer Setting

Image Management

3. Select Scan->eSmart Trainer.
Figure 3-105. Select eSmart Trainer

Performing an Exam

4. Press < or > to see more images in the selected module.
5. Select Return to exit the training module.
Figure 3-106. eSmartTrainer

Chapter 4
Customizing Your System
Describes how to view system information and

configure system settings.

Utility
Overview
Utility Menus provide the following functionality:
• General - Configure general system settings
• Settings - Configure system settings
• Image - Configure image settings
• Measure - Configure measurement settings
• System - View product information, software option and
configure log export storage device
• Connectivity - Configure system connectivity settings
• About - Software/hardware version and system patents

Utility
General
The General screen allows you to specify Facility Name, System
Language, Region, Package, Screen Lock Passcode, Data
Privacy Passcode, Date Format, Time Format, System Date and
System Time.
Figure 4-1. Utility - General

General (continued)
Table 4-1: General setting parameters
Preset Parameter Description
Facility Name Type the Hospital/Healthcare center/Institute Name.
System Language Select the appropriate language from the drop-down list.
Region Select the region from the drop-down list.

Note: If the region is changed, the system will shutdown.
Package Select the desired software package.
Screen Lock Passcode Press to create screen lock passcode (4 figures).
Data Privacy Passcode Press to create data privacy passcode (4 figures). When you press Review,
you need to input the passcode.
Date Format Select the appropriate date format from the drop-down list.
Time Format Select the appropriate time format from the drop-down list.
System Date Set the appropriate date.
System Time Set the appropriate time.
CAUTION It is the institution’s responsibility to remember the screen lock

passcode. Otherwise, you can not unlock the system. GE is
NOT responsible for the passcode.
CAUTION It is the institution’s responsibility to remember the data privacy

passcode. Otherwise, you can not review, backup, restore or
delete the patient information. GE is NOT responsible for the
passcode.

Utility
Settings
Common
Common tab of the Settings screen allows you to specify

parameters for the following:
• Video Length in Seconds
• 2nd ID
• Live Text Enable
• Image Store Area
• Live Scan Save
• Split Layout
• Brightness
• Lock Scanner After (minutes)
Figure 4-2. Settings - Common

Table 4-2: Setting - Common Parameters
Video length in seconds Select the length of video storage.
2nd ID Select Yes to enable 2nd ID field in patient screen.
Worklist Page First Select Yes to enable worklist page to show immediately when pressing
Home.
Live Text Enable Select Yes to enable text to be shown in live scanning mode.
Image Store Area Select Image Area or Full Screen for the image store area in the
drop-down menu.
Live Scan Save Select Image to store single frame image after pressing save during live
scanning; select Video to store cine loop after pressing save during live
scanning.
Split Layout Configure the layout of the split screen.
Brightness Select the brightness degree from the drop-down list.
Lock Scanner After (minutes) Select the time options to lock the scanner.
Note: You may also lock the screen by pressing Power button, then press
Lock Screen. To unlock the system, please slide to unlock.

Utility
Configure Page
Configure Page tab of the Settings screen allows you to

activate or deactivate the functions as follows:
• TGC
• M Mode
• Needle
• Split
• Zoom
• Guide
• eSmart Trainer
• Bodymark
• Measure
• Comment
Figure 4-3. Settings - Configure
NOTE: Only the activated function will be shown on the scanning

screen.

USB Accessories
USB Accessories tab of the Settings screen allows you to

configure the items as follows:
Footswitch:
• Left key
• Middle key
• Right key
Barcode:
• Barcode
• ReadTo
Figure 4-4. Settings - USB Accessories

Utility
Table 4-3: Setting-Footswitch Parameters
Left key Configure the left footswitch pedal for the selected application. Select the
functionality from the drop down menu.
Middle key Configure the middle footswitch pedal for the selected application. Select the
Right key Configure the right footswitch pedal for the selected application. Select the
Table 4-4: Barcode Parameters
Barcode Select On or Off to activate or deactivate the barcode reader.
ReadTo Select the barcode read information.

Miscellaneous
Miscellaneous tab of the Settings screen allows you to specify

Volume:
• Venue 50 speaker
Trainer Setting
• Available Trainer
Storage:
• Storage Location
Figure 4-5. Settings - Miscellaneous

Utility
Table 4-5: Setting - Miscellaneous Parameters
Venue 50 Speaker Select Mute, Low, Medium or High for Venue 50 speaker volume.
Trainer Setting Choose the desired eSmart Trainer region.
Storage Location View and configure storage location.
Check Select to check and restore current storage device.
Format Select to format current storage device.

Scan Configuration
Scan Configuration tab of the Settings screen allows you to

specify parameters for the following:
• Available Parameters
• Target Parameters
Figure 4-6. Settings - Scan Configuration
Table 4-6: Setting-Scan Configuration Parameters
Available Parameters The available image parameters for current mode.
Target Parameters The selected image parameters shown on the scanning screen. (Maximum of
3 parameters)
NOTE: Different probes and modes will have different available

parameters.

Utility
Image
Common
The Common screen allows you to configure the items as

follows:
• Thermal Name
• TIC
• TIS
• TIB
• Image
• Auto Zoom
• Image Style
• LCD Tint
Figure 4-7. Image - Common

Table 4-7: Image - Common settings
Thermal Name Select TIc, TIs, or TIb.

• TIc: Used when bone is near the skin surface as in transcranial
examination.
• TIs: Used when imaging soft tissue only.
• TIb: Used when bone is near the focus of the image as in the third trimester
OB examination.
Auto Zoom Select Yes or No to automatically zoom the images or not. It is only available
for image depth < 2cm.
Image Style Select Top or Center to show the image layout.
LCD Tint Select Natural Tint, Yellow Tint or Blue Tint from the drop-down list to show
the preferred image display tint.

Utility
User Define
User Define tab of the Settings screen allows you to specify

• Depth
• B Mode Parameters
• Color Flow Mode Parameters
• PDI Mode Parameters
• M Mode Parameters
• Create New/Overwrite
Figure 4-8. Image - User Define
NOTE: When performing an exam with the factory default preset, you
may modify and save the scanning parameter values. If you
switch to another preset and switch back to the modified one,
the parameter values will be restored to the factory default.

User Define (continued)
Create New/Overwrite
Create New/Overwrite allows you to configure your favorite
presets.
1. Configure the parameters.
2. Press Save.
3. Press Create New/Overwrite.
4. Press the blank box and name your favorite preset with the
soft keyboard.
Figure 4-9. UserDefine - Create New
5. Press Save to go back to Image screen.

NOTE: All the parameter values in the new preset are available for all
depth scanning. You may modify the value while scanning, if
needed.
NOTE: The new preset will be displayed in the Setting Favorites after
you press Save.
NOTE: You may create a maximum of 10 favorite applications.

Utility
Create New/Overwrite (continued)

If you have set your desired preset, it will be displayed under
Utility -> Image -> Application -> Available.
To overwrite the favorite preset:
1. Configure the parameters.
2. Press Save.
4. Select the appropriate tab to be overwritten.
5. Press Overwrite.
The new preset will overwrite the original one.
To delete the favorite preset:
2. Select the appropriate tab to be deleted.
3. Press Remove the remove the preset.
4. Press Save.

Application
The Application screen allows you to configure the items as

follows:
• Probe
• Available (application)
• Favorite (application)
• Default (application)
Figure 4-10. Image - Application
Table 4-8: Image - Application settings
Probe Select the available probe.
Available/Favorite Choose the available application to the favorite or vise verse.
Default Choose the desired application as the default one for the probe.

Utility
Measure
The Measure screen lists measurement configurations.
Obstetrics
The Obstetrics tab shows the OB measurement settings of the

Venue 50:
• OB Type
• EFW Format
• OB Table
• CUA/AUA
Figure 4-11. Measure - Obstetrics

Table 4-9: Obstetrics settings
OB Type Select which OB measurements and calculations studies to use: USA,

Europe, Tokyo, Osaka, or ASUM.
EFW Format Select the source used to calculate EFW (Estimated Fetal Weight): Hadlock,
Tokyo or Osaka.
OB Table Select Hadlock82 or Hadlock 84.
CUA/AUA Select the ultrasound age calculation method in this field. CUA: Composite
Ultrasound Age, regression calculation; AUA: Average Ultrasound Age, an
arithmetic average.

Utility
Measure
The Measure tab shows the configuration of measurement:
Figure 4-12. Measure - Measure
Table 4-10: Measure settings
Available Measurements The available measurements for current measurement application.
Measure Study The selected measurements (maximum of 12 measurements).

System
The System screen lists system information.
Figure 4-13. Utility - System
Table 4-11: Product Parameters
Product Name Display the system name.
HW Number Display converted hardware ID of the serial number.
Serial Number Display system serial number.
Table 4-12: SW Option Parameters
New key Add new software option keys when installing software options.
Installed keys Press to view the installed keys in the system.
Option status Press to view the installed software option status.
Remove Press to remove the installed keys.

Utility
Table 4-13: Remote Connection
Enable Connection From Turn on/off to connect/disconnect Gateway.

Gateway Note: The default Gateway connection is off.
Table 4-14: Log Export
Storage Press to choose the storage device.
Export Press to export the log to the storage device.

Connectivity
The Connectivity screen lists connectivity configurations.
TCP/IP
The TCP/IP screen shows the IP status of the Venue 50:

• IP Address
• Subnet Mask
• Default Gateway
Figure 4-14. Connectivity - TCP/IP
Table 4-15: IP settings
IP Address Type the IP Address.
Subnet Mask Type the subnet mask address.
Default Gateway Type the default gateway address.

Utility
Wired
The Wired screen shows the configuration of wired network:
Figure 4-15. Connectivity - Wired
Table 4-16: Wired settings
Enable DHCP Select to enable dynamic IP Address selection.

Wireless
The Wireless screen shows the configuration of wireless

network:
Figure 4-16. Connectivity - Wireless
Table 4-17: Wireless Connection
Preset
Parameter Description
SSID Select Scan, the list of the available wireless network displays. Select the wireless
network that needs to be connected.
Network Select OPEN, WPA2-PSK or WPA-PSK for Network Authentication

Authentication
Data Encryption Select WEP or NONE for Data Encryption type if the Network Authentication is
OPEN.
Select AES or TKIP if the Network Authentication is WPA2-PSK or WPA-PSK.
Network Key Type the Network Key.
Key Index Select 1 to 4 from the drop-down menu for Key Index.
NOTE: It is available only when the Network Authentication is OPEN and the Data
Encryption is WEP.

Utility
DICOM
The DICOM screen shows the configuration of DICOM:
Figure 4-17. Connectivity - DICOM
Table 4-18: DICOM Worklist settings
IP Address Type the IP Address of the worklist server.
AE Title Type the calling AE Title of the worklist server.
Port Type the port of the worklist server.
Table 4-19: DICOM Search Criteria settings
Modality Type the exam modality.
Data Range Type the date range.

Table 4-19: DICOM Search Criteria settings
Note: Only one or two bytes can be input in the modality cell. Note: The default value of date range is 0, and
the maximum value is 60. Set date range to 0, the Scheduled Procedure Step Start Date will include today
only. Set the date range to X (an integer number between 0 and 60), the Scheduled Procedure Step Start
Date will include X days prior and from today.
Table 4-20: DICOM Image Storage settings
IP Address Type the IP Address of the DICOM image server.
AE Title Type the calling AE Title of the DICOM image server.
Port Type the port of the DICOM image server.
Enable MultiFrame Select to enable multiframe DICOM.

DICOM
Table 4-21: DICOM Local AE Title
DICOM local AE Title Type the local DICOM called AE Title.

Utility
QuickSave
The QuickSave screen shows the configuration of QuickSave:
Figure 4-18. Connectivity - QuickSave
Table 4-22: QuickSave settings
IP Address Type the IP Address of the shared folder.
User Name Type the User Name.
Password Type the password.
Shared folder Type the Shared folder name.

DataFlow
The DataFlow screen shows the configuration of D1 and D2:
Figure 4-19. Connectivity - DataFlow
Table 4-23: Measure settings
D1, D2 DataFlow button to be configured.
Available parameters The available storage media.
Target parameters The selected storage media.

Utility
Backup/Restore
The Backup/Restore screen allows you to configure the items

as follows:
• Storage
• Backup/Restore
• Patient data/images/videos
• User defined presets
• Configuration settings
• Backup
• Restore
• Delete
• Backup remind interval
Figure 4-20. Connectivity - Backup/Restore

Backup/Restore (continued)
Table 4-24: Image - Backup/Restore settings
Storage Select the available storage device.
Backup Backup the Patient data/images/videos, User defined presets or

Configuration settings from HDD to the selected storage device.
Restore Restore the Patient data/images/videos, User defined presets or

Configuration settings from the selected storage device to the HDD.
Delete Delete the Patient data/images/videos, User defined presets or Configuration

settings from the HDD.
Backup remind interval Choose One day, One week or One month from the menu.
NOTE: If you have set the data privacy passcode, you need to input the
passcode to backup, restore or delete the information.
CAUTION It is the institution’s responsibility to remember the data privacy

passcode. Otherwise, you can not review, backup, restore or
delete the information. GE will NOT aid in the recovery of the
information.

Utility
About
The About screen allows you to view software version,
hardware versions and the system patents.
Figure 4-21. Utility - About
Table 4-25: Software version Parameters
Version View software version.
SSD Store View the SSD available and used storage capacity.
Region Region of the preset.
Build Date View software build date.
Table 4-26: Hardware version Parameters
Version View hardware version of main boards.


Chapter 5
Probes and Biopsy
This chapter consists of the information for each probe

and describes some special concerns, biopsy kits and
accessories as well as basic procedures for attaching a
biopsy guide to the different types of probes.

Probes and Biopsy
Probe Overview
Ergonomics
Probes have been ergonomically designed to:
• Handle and manipulate with ease
• Connect to the system with one hand
• Be lightweight and balanced
• Have rounded edges and smooth surfaces
• Stand up to typical wear by cleaning and disinfectant
agents, contact with approved gel, etc.
Cables have been designed to:
• Connect to system with appropriate cable length
Cable handling
Take the following precautions with probe cables:
• Keep free from wheels
• Do not bend the cable acutely
• Avoid crossing cables between probes

Probe Overview
Probe orientation
Each probe is provided with an orientation marking. This mark is
used to identify the end of the probe corresponding to the side of
the image having the orientation mark on the display.
Figure 5-1. Orientation Marking on Probe (Example)
1. Orientation Mark

Probes and Biopsy
Labeling
Each probe is labeled with the following information:
• Seller's name and manufacturer
• GE part number
• Probe serial number
• Month and year of manufacture
• Probe designation-provided on the probe grip and the top of
the connector housing, so it is easily read when mounted on
the system and is also automatically displayed on the
screen when the probe is selected.
Figure 5-2. Displayed Probe Information
1. Probe Information Location
Probe Naming Conventions

Table 5-1: Probe Naming Convention
Type Frequency Connector Type
C=Convex “12” in probe SC

L=Linear “12L-SC”
S=Sector

Probe Overview
Probe Usage
For details on connecting, activating, deactivating,
disconnecting, transporting and storing the probes, See ‘Probes’
Care and Maintenance
Inspecting Probes
Perform After Each Use

Inspect the probe's lens, cable, casing, and connector. Look for
any damage that would allow liquid to enter the probe. If any
damage is found, do not use the probe until it has been
inspected and repaired/replaced by a GE Service
Representative.
NOTE: Keep a log of all probe maintenance, along with a picture of any
probe malfunction.
Environmental Requirements
Probes should be operated, stored, or transported within the

parameters outlined below.
CAUTION Ensure that the probe face temperature does not exceed the
normal operation temperature range.
Table 5-2: Probe Environmental Requirements
Operational Storage Transport
Temperature 3 - 40°C -5 - 50°C -5 - 50°C

37 - 104°F 23 - 122°F 23 - 122°F
Humidity 30 - 80% 10 - 90% 10 - 90%

non-condensing non-condensing non-condensing
Pressure 700 - 1060hPa 700 - 1060hPa 700 - 1060hPa

Probes and Biopsy
Probe Safety
Handling precautions
WARNING Ultrasound probes are highly sensitive medical instruments

that can easily be damaged by improper handling. Use care
when handling and protect from damage when not in use. DO
NOT use a damaged or defective probe. Failure to follow
these precautions can result in serious injury and equipment
damage.
Electrical shock hazard
Electrical The probe is driven with electrical energy that can injure the
Hazard patient or operator if live internal parts are contacted by
conductive solution:
• DO NOT immerse the probe into any liquid beyond the
level indicated by the immersion level diagram. Refer to
the immersion illustration in the Probe Cleaning Process
section. Never immerse the probe connector or probe
adaptors into any liquid.
• DO NOT drop the probes or subject them to other types of
mechanical shock or impact. Degraded performance or
damage such as cracks or chips in the housing may result.
• Prior to each use, visually inspect the probe lens and case
area for cracks, cuts, tears, and other signs of physical
damage. DO NOT use a probe which appears to be
damaged until you verify functional and safe performance.
You must perform a more thorough inspection, including
the cable, strain relief, and connector, each time you clean
the probe.
• Before inserting the connector into the probe port, inspect
the probe connector pins. If a pin is bent, do not use the
probe until it has been inspected and repaired/replaced by
a GE Service Representative.
• DO NOT kink, tightly coil, or apply excessive force on the
probe cable. Insulation failure may result.
• Electrical leakage checks should be performed on a routine
basis by GE Service or qualified hospital personnel. Refer
to the service manual for leakage check procedures.

Probe Overview
Mechanical hazards
CAUTION A defective probe or excessive force can cause patient injury or

probe damage.
• Observe depth markings and do not apply excessive force
when inserting or manipulating intercavitary probes.
• Inspect probes for sharp edges or rough surfaces that
could injure sensitive tissue.
• DO NOT apply excessive force to the probe connector
when inserting into the probe port. The pin of a probe
connector may bend.

Probes and Biopsy
Special handling instructions
Using protective sheaths
CAUTION Protective barriers may be required to minimize disease

transmission. Probe sheaths are available for use with all
clinical situations where infection is a concern. Use of legally
marketed, sterile probe sheaths is strongly recommended for
intra-cavitary and intra-operative procedures. Use of legally
marketed, sterile, pyrogen free probe sheaths is REQUIRED
for neurological intra-operative procedures.
Instructions. Custom made sheaths are available for each

probe. Each probe sheath kit consists of a flexible sheath used
to cover the probe and cable and elastic bands used to secure
the sheath.
Sterile probe sheaths are supplied as part of biopsy kits for
those probes intended for use in biopsy procedures. In addition
to the sheath and elastic bands, there are associated
accessories for performing a biopsy procedure which are
included in the kit. Refer to the biopsy instructions for the
specific probes in the ‘Preparing for a Biopsy’ on page 5-25 for
further information.
Reordering. To reorder sheaths, please contact your local
distributor or the appropriate support resource.
CAUTION Devices containing latex may cause severe allergic reaction in

latex sensitive individuals. Refer to FDA's March 29, 1991
Medical Alert on latex products.
CAUTION DO NOT use pre-lubricated condoms as a sheath. In some

cases, they may damage the probe. Lubricants in these
condoms may not be compatible with probe construction.
CAUTION DO NOT use an expired probe sheath. Before using probe

sheaths, verify whether the term of validity has expired.

Probe Overview
Endocavitary Probe Handling Precautions
If the sterilization solution comes out of the endocavitary probe,

please follow the cautions below.
CAUTION Sterilant Exposure to Patient (e.g., Cidex)—Contact with a

sterilant to the patient’s skin or mucous membrane may cause
an inflammation. If this happens, refer to the sterilant’s
instruction manual.
Sterilant Exposure from Probe Handle/Connector to
Patient (e.g., Cidex)—DO NOT allow the sterilant to contact
the patient. Only immerse the probe to its specified level.
Ensure that no solution has entered the probe’s handle before
scanning the patient. If sterilant comes into contact with the
patient, refer to the sterilant’s instruction manual.
Endocavitary Probe Point of Contact—Refer to the
sterilant’s instruction manual.

Probes and Biopsy
Probe handling and infection control

This information is intended to increase operator awareness of
the risks of disease transmission associated with using this
equipment and provide guidance in making decisions directly
affecting the safety of the patient as well as the equipment
operator.
Diagnostic ultrasound systems utilize ultrasound energy that
must be coupled to the patient by direct physical contact.
Depending on the type of examination, this contact occurs with a
variety of tissues ranging from intact skin in a routine exam to
recirculating blood in a surgical procedure. The level of risk of
infection varies greatly with the type of contact.
One of the most effective ways to prevent transmission between
patients is with single use or disposable devices. However,
ultrasound transducers are complex and expensive devices that
must be reused between patients. It is very important, therefore,
to minimize the risk of disease transmission by using barriers
and through proper processing between patients.
CAUTION Risk of infection. ALWAYS clean and disinfect the probe

between patients to the level appropriate for the type of
examination and use FDA-cleared probe sheaths where
appropriate.
CAUTION Adequate cleaning and disinfection are necessary to prevent

disease transmission. It is the responsibility of the equipment
operator to verify and maintain the effectiveness of the infection
control procedures in use. Always use sterile, legally marketed
probe sheaths for intra-cavitary and intra-operative procedures.
For neurological intra-operative procedures, use of a legally
marketed, sterile, pyrogen free probe sheath is REQUIRED.
Probes for neuro surgical use must not be sterilized with liquid
chemical sterilants because of the possibility of neuro toxic
residues remaining on the probe.

Probe Overview
Probe Cleaning Process
Cleaning Probes
To clean the probe:

NOTE: Do not immerse the probe into any liquid beyond the level
specified for that probe (See Figure 5-3 on page 5-12 for more
information.). Never immerse the transducer connector into any
liquid.
1. Inspect the probe’s lens, cable, casing, and connector for
cracks, cuts, tears, and other signs of physical damage.
2. Disconnect the probe from the ultrasound console. Remove
all coupling gel from the probe by wiping with a soft cloth
and rinsing with flowing water.
NOTE: DO NOT wipe the probe with a dry cloth.
3. Soak the probe head in water. Scrub the probe as needed
using a soft sponge, gauze, or cloth to remove all visible
residue from the probe surface.
CAUTION Take extra care when handling the lens face of the
ultrasound transducer. The lens face is especially sensitive
and can easily be damaged by rough handling. NEVER
use excessive force when cleaning the lens face.
4. Rinse the probe with enough clean, potable water.

5. Air dry or dry with a soft cloth.
6. After cleaning, inspect the probe’s lens, cable, casing and
connector. Look for any damage that would allow liquid to
enter the probe. Also, inspect the probe functionality by live
scan. If any damage is found, do not use the probe until it
has been inspected and repaired/replaced by a GE service
representative.

Probes and Biopsy
Cleaning Probes (continued)
Figure 5-3. Probe Immersion Levels
1. Fluid Level

Probe Overview
Disinfecting probes
Perform After Ultrasound probes can be disinfected using liquid chemical

Each Use germicides. The level of disinfection is directly related to the
duration of contact with the germicide. Increased contact time
produces a higher level of disinfection.
Table 5-3: Description of Pictogram on Care Card
Pictogram Description
“ATTENTION” - Consult accompanying documents is intended to alert the

operator to refer to the operator manual or other instructions when complete
information cannot be provided on the label.
“CAUTION” - Dangerous voltage (the lightning flash with arrowhead) is used to

indicate electric shock hazards.
Biohazard - Patient/operator infection due to contaminated equipment.

Usage
• Cleaning and care instructions
• Sheath and glove guidelines
Ultrasound probes are highly sensitive medical instruments that can easily be
damaged by improper handling. Use care when handling and protect from
damage when not in use.
Do not immerse the probe into any liquid beyond the level specified for that
probe. Refer to the user manual of the ultrasound system.
Since there is a possibility of having negative effects on the probe, strictly

observe the specified immersing time by the germicide manufacturer. Do not
immerse the probe in liquid chemical germicides more than the time prescribed
in the care card.
“Consult accompany document” - Refer to the ultrasound system user manual

for important probe care and cleaning instruction.

Probes and Biopsy
Disinfecting probes (continued)
CAUTION Review the probe care card that is packed with each probe. For
the GE approved probe disinfectants, please refer to the probe
care card.
http://www3.gehealthcare.com/Products/Categories/
Ultrasound/Ultrasound_Probes#cleaning
CAUTION In order for liquid chemical germicides to be effective, all visible

residue must be removed during the cleaning process. As
described earlier before attempting disinfection, thoroughly
clean the probe.
You MUST disconnect the probe from the Venue 50 prior to
cleaning/disinfecting the probe. Failure to do so could damage
the system.
DO NOT soak probes in liquid chemical germicide for longer
than is stated by the germicide instructions for use. Extended
soaking may cause probe damage and early failure of the
enclosure, resulting in possible electric shock hazard.
1. Prepare the germicide solution according to the

manufacturer's instructions. Be sure to follow all precautions
for storage, use and disposal.
2. Place the cleaned and dried probe in contact with the
germicide for the time specified by the germicide
manufacturer. High-level disinfection is recommended for
surface probes and is required for endocavitary and
intraoperative probes (follow the germicide manufacturer's
recommended time).
CAUTION Probes for neuro surgical intra-operative use must NOT be

sterilized with liquid chemical sterilants because of the
possibility of neuro toxic residues remaining on the probe.
Neurological procedures must be done with the use of
legally marketed, sterile, pyrogen free probe sheaths.
3. After removing from the germicide, rinse the probe following

the germicide manufacturer's rinsing instructions. Flush all
visible germicide residue from the probe and allow to air dry.

Probe Overview
Disinfecting probes (continued)
Biological
Hazard
WARNING CREUTZFIELD-JACOB DISEASE

Neurological use on patients with this disease must be
avoided. If a probe becomes contaminated, there is no
adequate way to disinfect the probe.
WARNING Ultrasound transducers can easily be damaged by improper

handling and by contact with certain chemicals. Failure to
follow these precautions can result in serious injury and
equipment damage.
• Do not immerse the probe into any liquid beyond the level
specified for that probe. Never immerse the transducer
connector or probe adapters into any liquid.
• Avoid mechanical shock or impact to the transducer. Do
not apply excessive bending or pulling force to the cable.
• Transducer damage can result from contact with
inappropriate coupling or cleaning agents.
• Do not soak or saturate transducers with solutions
containing alcohol, bleach, ammonium chloride
compounds or hydrogen peroxide.
• Avoid contact with solutions or coupling gels containing
mineral oil or lanolin.
• Avoid temperatures above 60°C.
• Inspect the probe prior to use for damage or degeneration
to the housing, strain relief, lens and seal. Do not use a
damaged or defective probe.

Probes and Biopsy
Coupling gels
WARNING Do not use unrecommended gels (lubricants). They may

damage the probe and void the warranty. Please refer to the
probe care card for GE approved probe gels.
Applying In order to assure optimal transmission of energy between the

patient and probe, a conductive gel or couplant must be applied
liberally to the patient where scanning will be performed.
CAUTION Do not apply gel to the eyes. If there is gel contact to the eye,
flush eye thoroughly with water.
Precautions Coupling gels should not contain the following ingredients as

they are known to cause probe damage:
• Methanol, ethanol, isopropanol, or any other alcohol-based
product
• Mineral oil
• Iodine
• Lotions
• Lanolin
• Aloe Vera
• Olive Oil
• Methyl or Ethyl Parabens (para hydroxybenzoic acid)
• Dimethylsilicone
• Polyether glycol based
• Petroleum
Sterile Ultrasound Procedures

ONLY ultrasound gel that is labeled as sterile, is sterile.
Ensure you always use sterile ultrasound gel for those
procedures that require sterile ultrasound gel.
Once a container of sterile ultrasound gel is opened, it is no
longer sterile and contamination during subsequent use is
possible.

Probe Overview
Planned Maintenance
The following maintenance schedule is suggested for the

system and probes to ensure optimum operation and safety.
Table 5-4: Planned Maintenance Program
Do the Following Daily After Each Use As Necessary
Inspect the Probes X X X
Clean the Probes X X
Disinfect Probes X X

Probes and Biopsy
Returning/Shipping Probes and Repair Parts
US Department of Transportation and GE Medical Systems

policy requires that equipment returned for service MUST be
clean and free of blood and other infectious substances.
When you return a probe or part for service (Field Engineer or
customer), you need to clean and disinfect the probe or part
prior to packing and shipping the equipment.
Ensure that you follow probe cleaning and disinfection
instructions provided in the Basic User Manual.
This ensures that employees in the transportation industry as
well as the people who receive the package are protected from
any risk.

Probe Discussion
Probe Discussion
Introduction
The Venue 50 supports the following types of probes:
• Curved Array (Convex). Curved Array (Convex) probes,
including `micro' convex, are usually designated by the
prefix/suffix "C"; the endocavitary probe is designated by the
prefix/suffix "E".
• Linear Array. Linear Array probes are designated by the
prefix/suffix "L".
• Phased Array Sector. Phased Array Sector probes are
designated by the prefix/suffix "S".

Probes and Biopsy
Probe Applications
Table 5-5: Probe Indications for Use
Probe Application 3S-SC 12L-SC 4C-SC L8-18i-SC E8CS-SC 10C-SC
Peripheral Vascular x x
Fetal/OB x x x
Abdominal (GYN & x x x x x x

Urology)
Pediatric x x x x x
Small Organ (breast, x x x

testes, thyroid)
Neonatal Cephalic x x x x
Adult Cephalic x
Cardiac (adult & pediatric) x
Conventional x x x x
Musculoskeletal
Superficial x x x
Musculoskeletal
Thoracic/Pleural x x x x x
Intraoperative (abdominal, x x x x x
thoracic and peripheral)
Transvaginal x
Ophthalmic x x x
Tissue Biopsy/ Fluid x x x x x

Drainage
Vascular Access x x
Nonvascular x x x
NOTE: Ophthalmic is not available for Japan.

Probe Discussion
Probe Specifications
Table 5-6: System Probe Definitions
Doppler Frequency (MHz)

Center Image
Probe Designation Frequency [MHz) Normal Penetration
3S-SC 2.0 ± 20% 2.2 1.8
12L-SC 7.5 ± 20% 4.4 4.0
4C-SC 3.1 ± 10% 3.08 2.5
L8-18i-SC 9.5 ± 20% 8.7 5.71
E8CS-SC 6.5 ± 20% 5.0 4.0
10C-SC 8.0 ± 20% 5.0 4.0
Probe Slice Thickness Specifications

Table 5-7: System Probe Definitions
Probe Slice Thickness
3S-SC <=10mm
12L-SC <=8mm
4C-SC <=8mm
L8-18i-SC <=8mm
E8CS-SC <=13mm
10C-SC <=13mm

Probes and Biopsy
Probe Illustration
Table 5-8: Sector Probes
Probe Illustration
3S-SC
Table 5-9: Linear Array Probes
Probe Illustration Probe Illustration
12L-SC L8-18i-SC
Table 5-10: Curved Array (Convex) Probes
Probe Illustration Probe Illustration
4C-SC 10C-SC
E8CS-SC

Precautions Concerning the Use of Biopsy Procedures
WARNING Do not freeze the image during a biopsy procedure. The image
must be live to avoid a positioning error.
Biopsy guidezones are intended to assist the operator in
determining optimal probe placement and approximate the
needle path. However, actual needle movement is likely to
deviate from the guideline. Always monitor the relative
positions of the biopsy needle and the subject mass during the
procedure.
CAUTION The use of biopsy devices and accessories that have not been
evaluated for use with this equipment may not be compatible
and could result in injury.

Probes and Biopsy
Precautions Concerning the Use of Biopsy Procedures (continued)
CAUTION The invasive nature of biopsy procedures requires proper

preparation and technique to control infection and disease
transmission. Equipment must be cleaned as appropriate for
the procedure prior to use.
• Follow the probe cleaning, disinfection procedures and
precautions to properly prepare the probe.
• Follow the manufacturer's instructions for the cleaning of
biopsy devices and accessories.
• Use protective barriers such as gloves and probe sheaths.
• After use, follow proper procedures for decontamination,
cleaning, and waste disposal.
CAUTION Improper cleaning methods and the use of certain cleaning and
disinfecting agents can cause damage to the plastic
components that will degrade imaging performance or increase
the risk of electric shock.
See ‘Probe Safety’ on page 5-6 for more information.
WARNING NEVER reuse the TR5° disposable biopsy guide attachment

and disposable sterile Ultra-Pro II Needle guide kits.

Displaying the Guidezone

Activate the Biopsy Kit by selecting Guide from the B-Mode
Menu.
The available biopsy options appear when Biopsy Kit is
selected. There are fixed and adjustable angle biopsy kits
available with the Venue 50 depending on the probe. Select the
desired biopsy kit.

Probes and Biopsy
Displaying the Guidezone (continued)
Figure 5-4. Biopsy Guidezones
The biopsy guidezone represents a path of the needle. The dots

which make up the guidezones indicates the depth readout
where:
• White represents 1 cm increments.
• Red represents 5 cm increments.
The display should be carefully monitored during a biopsy for
any needle deviation from the center line or guidezone.
Before scanning, verify the needle can be visualized within the
imaging plane. Use the appropriate needle to reach target area.

Displaying the Guidezone (continued)

The needle may vary from the center line or guidezone for
various reasons:
• Needle barrel to needle clearance or strength.
• Bracket manufacturing tolerance.
• Needle deflection due to tissue resistance.
• Needle size chosen. Thinner needles may deflect more.
Table 5-11: Biopsy Guide Availability
Multi-Angle
Probe Fixed Angle
MBX1 MBX2 MBX3
3S-SC 4.0cm 5.5cm 8.0cm
12L-SC 1.5cm 2.5cm 3.5cm
4C-SC 4.1cm 6.07cm 10.05cm
E8CS-SC 15.3 (TR5) 15200

(reusable)
DANGER Failure to match the guidezone displayed to the guide may

cause the needle to track a path outside the zone.
It is extremely important that when using the adjustable angle
biopsy guides, the angle displayed on the screen matches the
angle set on the guide. Otherwise, the needle will not follow the
displayed guidezone which could result in repeated biopsies or
patient injury.

Probes and Biopsy
Preparing the Biopsy Guide Attachment

Convex, Sector and Linear probes have optional biopsy guide
attachments for each probe. The guide consists of a
non-disposable bracket to attach to the probe, and a disposable
needle clip to attach to the bracket, sheath, gel (sterile gel if
necessary) and disposable needle barrels.
The disposable needle barrels are available for a variety of
needle sizes.
CAUTION Please refer to the manufacturer's instructions included in the

biopsy kit.
The bracket is packaged non-sterile and is reusable. To avoid

possible patient contamination, ensure bracket is properly
cleaned, sterilized or disinfected before each use.
Disposable components are packaged sterile and are single-use
only. Do not use if integrity of packing is violated or if expiration
date has passed.

Fixed Needle Biopsy Guide Assembly
WARNING DO NOT use the needle with the catheter (soft tube). There is a
possibility of breaking the catheter in the body.
CAUTION Before inserting the needle, scan the patient to determine the
correct puncture depth and site. Only the sterile/sanitary
sheath, sterile gel and rubber band are on the probe during the
pre-needle placement scanning.
Preparation
To prepare the endocavitary probe for use:
1. Remove the probe from the box and carefully examine it for
any damage.
2. Clean, then disinfect the probe.
NOTE: Ensure that protective gloves are worn.

Probes and Biopsy
Installing the sheath
To install the sheath:

1. Remove the sheath from the package. Do not unroll the
sheath.
NOTE: Remember to rinse all sanitary probe sheaths of powder
before placing on the probe. Powder can degrade the
displayed image.
2. Place an adequate amount of ultrasound gel inside the
sheath tip (the gel is between the sheath inner surface and
the probe aperture).
NOTE: Ensure that only acoustic coupling gel is used for this
purpose.
3. Place the sheath tip over the probe aperture and then pull
the sheath end toward the probe handle.
4. Inspect the sheath for nicks, cuts or tears.
a b
Figure 5-5. Endocavitary Probe with Sheath
a. Sanitary Sheath
b. Probe Body
c. Probe Handle
5. Rub a finger over the tip of the probe to ensure all air
bubbles have been removed.

Endocavitary Probe Biopsy Guide Preparation

1. If a biopsy is to be performed, snap the metal or plastic
biopsy guide on to the probe over the sheath.
CAUTION Patient injury or repeated biopsies may result. The needle

placement will not be as intended if the needle guide is not
properly seated and secure.
Figure 5-6. Disposable Biopsy Guide 5 degree Angle
a
Figure 5-7. Reusable Biopsy Guide
a. Fix with a screw

2. Place an adequate amount of ultrasound gel on the gel-filled
sheath tip’s outer surface.
3. Ensure the guide is properly seated and secure by pushing
forward on the needle insertion end of the guide until the
attachment node is firmly in place in its hole.

Probes and Biopsy
Multi Angle Biopsy Guide Assembly
WARNING DO NOT attempt to use the biopsy bracket and needle guide
until the manufacturer's instructions, provided with the biopsy
bracket and needle guide in the kit, have been read and
thoroughly understood.
1. Scan the patient and identify the target for biopsy. Move the
probe to locate the target to the center of the image. Enable
the system biopsy guidezone and try guidezone angles
MBX1 to MBX3 to decide the best angle setting for needle
path.
Figure 5-8. Example
2. Pull up on the knob (Figure 5-9 a) to freely move the needle

guide attachment. Align the knob with the selected position
of the needle guide attachment.
Push the knob down (Figure 5-9 b) into the desired slot to
secure the angle position of the needle guide attachment.
Figure 5-9. Pull up and push down the knob

Multi Angle Biopsy Guide Assembly (continued)
3. Fit a convex of the biopsy bracket (a) in a concave of the

probe (b).
Figure 5-10. Probe/Bracket Alignment
Hold the side (a) and tuck down the needle guide side (b)
until it clicks or locks in place.
Figure 5-11. Probe/Multi-angle Bracket Alignment 2
4. Place an adequate amount of coupling gel on the face of the

probe.

Probes and Biopsy
5. Place the proper sanitary sheath tightly over the probe and
biopsy bracket. Use the rubber bands supplied to hold the
sheath in place.
Figure 5-12. Applying Sanitary Sheath
6. Snap the needle clip onto the biopsy guide bracket.
Figure 5-13. Snap the needle guide

7. Push the locking mechanism towards the bracket to secure

the lock. Make sure the needle guide is firmly attached to
the bracket.
Figure 5-14. Lock the Needle guide
8. Choose the desired gauge (size) needle barrel. Twist it back

and forth to remove it from the plastic tree.
Figure 5-15. Needle Barrel
9. Place the needle barrel into the needle clip with the desired
gauge facing the needle clip and snap into place.
Figure 5-16. Needle Barrel Installation

Probes and Biopsy
Remove the biopsy guide

1. Hold the other side and push out the needle clip attachment
side. See Figure 5-17.
Figure 5-17. Remove the biopsy guide
CAUTION Avoid finger nail contact with the probe lens to prevent
damage.

Releasing the needle
According to the following procedure, you remove the needle

from a probe and an assembly without moving the needle.
Figure 5-18. Release the needle from assembly
a. Push the knob portion of a sleeve in the direction of the

arrow.
b. The needle is released from the assembly.
c. Push the probe and the assembly in the direction of the
larger arrow to remove the needle.

Probes and Biopsy
Biopsy Needle Path Verification

To verify that the path of the needle is accurately indicated within
the guidezone on the system monitor, perform the following:
• Properly install the bracket and biopsy guide.
• Scan in a container filled with water (47°C).
• Display the biopsy guidezone on the monitor.
• Ensure that the needle echo falls within the guidezone
markers.

The Biopsy Procedure
WARNING Biopsy procedures must only be performed on live images.
CAUTION Before activating the Guide, please make sure to select

Interventional related preset first.
1. Place coupling gel on the scanning surface of the probe/

sheath/biopsy guide assembly.
2. Activate the biopsy guidezone on the system by pressing
Guide. When using multi-angle guides, ensure that the
proper guidezone angle is displayed.
Figure 5-19. Biopsy multi-angle guides

Probes and Biopsy
The Biopsy Procedure (continued)

3. Scan to locate the target. Center the target in the electronic
guidezone path.
NOTE: Enabling color flow would allow for visualization of the
vascular structure around the area to be biopsied.
4. Place the needle in the guide between the needle barrel and
needle clip. Direct it into the area of interest for specimen
retrieval.

Post Biopsy
When the biopsy is complete, remove the needle barrel, needle
clip and probe sheath. Properly dispose of these items in
accordance with current facility guidelines.
Clean and disinfect the probe. See ‘Probe Cleaning Process’ on
page 5-11 for more information.
The biopsy bracket can be cleaned and disinfected in a
recommended disinfecting agent and reused.
CAUTION When the biopsy needle guide kit is opened, all parts must be
discarded after the procedure whether they have been used or
not.

Probes and Biopsy
Preparing for Surgery/Intra-operative Procedures

Preparing the transducer for interventional use follows the same
sterile procedure as for biopsy use except that no biopsy
attachments are used. See ‘Preparing the Biopsy Guide
Attachment’ on page 5-28 for more information. Sterile gel is
applied to the transducer face and a sterile sheath completely
covers the transducer and cable which has first undergone a
thorough cleaning and high-level disinfection.
The invasive nature of biopsy procedures requires proper
preparation and technique to control infection and disease
transmission. Equipment must be cleaned as appropriate for the
procedure prior to use.
CAUTION For surgery/intra-operative procedures, a sterile environment is

required. Therefore, both the operator and probe need to be
sterile.

Preparing for Surgery/Intra-operative Procedures (continued)

To ensure a sterile environment during the procedure, it is
recommended that this be a two-person job.
1. Perform a high level disinfection of the probe.
2. The scanner (surgeon, sonographer, etc.) should be sterile
and gloved.
3. Place an adequate amount of sterile coupling gel on the
face of the probe.
4. Place the proper sterile sheath over the probe and cord.
Figure 5-20. Applying Sterile Sheath
5. Depending on the type of procedure, use either sterile water

or sterile gel on the sheath cover.
NOTE: Follow your institutions guidelines on post surgery/
intra-operative procedures for probe cleaning and disinfection.

Probes and Biopsy

Chapter 6
User Maintenance
This chapter supplies system data, assistance

information, system care and maintenance instructions.

User Maintenance
System Data
Features/Specifications
NOTE: Some feature(s)/probe(s) may not be available in some
country(ies)/region(s), please contact your sales representative
for detailed information.
Table 6-1: General Specification
Console Dimensions Docking Cart Dimensions

• Height: 282 mm (11.1 in) • Height: 1152-1442 mm (45.4-56.8 in)
• Width: 274 mm (10.8 in) • Width: 510mm (20.1 in)
• Depth: 56 mm (2.2 in) • Depth: 480 mm (18.9 in)
• Weight: 4.0 kg (8.8 lbs.) with probe • Weight: 28.5 kg (62.8 lbs.)
Console Electrical Power Docking Station Dimensions

• Voltage:100-240 V AC • Height: 375 mm (14.7 in)
• Frequency: 50/60 Hz • Width: 463 mm (18.2 in)
• Power: Max. 180VA • Depth: 243 mm (9.5 in)
• Weight: 4.6 kg (10.1 lbs.)
Console Design
• Tablet Style
• Lithium-ion Battery Pack
• Single probe port
• Integrated speaker
• Docking cart (optional)
• Tabletop docking station (optional)
Table 6-2: User Interface
Touch Screen Display Screen

• Multi-touch user-interface with gesture recognition • 12.1 in High-Resolution Color LCD
• Mode-specific controls • Display: 1024x768
• Alphanumeric Keyboard
• Measurement Hard Keys
• Annotations • On/Off button
• Body marks
• Utility settings LED
• Patient information entry • Battery life

System Data
Table 6-3: System Overview
Transducer Types Display Annotation

• Linear Array • Institution/Hospital Name
• Phased Array • Date: MM/DD/YY, DD/MM/YY and YY/MM/DD
• Convex Array • Time: configurable 12 or 24 hrs
• Patient Name: Last, First
Operating Modes • Patient ID: 16 characters
• B-Mode • Power Output Readout
• M-Mode — MI: Mechanical Index
• Color Flow Mode (CFM) — TIS, TIB, TIC: Thermal Index
• Power Doppler Imaging (PDI) • System Status (real-time or frozen)
• Needle Recognition • Probe Orientation Marker: Coincides with a
probe orientation marking on the probe.
Standard Features • Loop replay
• Automatic Tissue Optimization (ATO) • Measurement Results Window
• CrossXBeamTM • Probe Type
• Measurement and calculation, editable • Preset Name
• Pinch Zoom • Imaging Parameters by Mode (current mode)
• Split window — B-mode: Gain, Image Depth, TGC (4 plots),
• Configurable menu Others (configurable, 3 at most)
• Standard CINE Memory — M-mode: M Gain, Image Depth, M sample
• Loops storage from memory line, TGC (4 plots), Configurable (3 at most)
• Internal solid-state drive (SSD) — Color Flow Mode: Color Gain, Image Depth,
• Patient data protection Color ROI box, TGC (4 plots), Configurable (3 at
• User-define preset most)
— Power Doppler Imaging Mode: PDI Gain,
Software Options Image Depth, PDI ROI box, TGC (4 plots),
• M-mode Configurable (3 at most)
• DICOM — Needle Recognition Mode: B Gain, Needle
• OB Package Gain, Beam Angle, Needle Direction, TGC (4
• Needle Recognition plots)
• Ophthalmic — CINE Mode: Previous Frame, Next Frame,
• eSmart Trainer Play/Pause
• B Scale Markers: Depth
Hardware Options • System Messages Display
• Docking Cart • Annotation Library: 18-21 preset labels, defined
• Tabletop Docking Station by the application
• Probes • Customizable annotations: 12 available for each
• 3-probe port application
• Extended life battery • Keyboard for free test on screen
• Comments available in Live scan mode and
Media & Peripheral Options Freeze mode
• USB thermal B&W printer • Body marks available for each application
• USB Memory Stick • Arrows available in Live scan mode and Freeze
• SD card mode
• Footswitch • Battery status
• Barcode reader • Biopsy Guide Line and Zone
• Wireless card • Configurable user-interface with anatomy
specific presets
Display Modes
• Live image or Stored image
• Full size or split screen

User Maintenance
Table 6-4: System Parameters
System Setup • Operation Error Message Display

• Factory default application data • Patient Name Format: Last, First
• Languages setup for UI: English, German, French, • System Boot Up: <16 sec
Italian, Spanish, Portuguese, Simplified Chinese, • Probe Loading: <3 sec
Swedish, Norwegian, Danish, Finnish, Greek,
Russian, Dutch, Japanese
• Languages for Manuals: English, French, Spanish,
German, Italian, Portuguese, Japanese, Chinese,
Czech, Danish, Dutch, Estonian, Finnish, Greek,
Hungarian, Latvian, Lithuanian, Norwegian, Polish,
Russian, Slovakian, Swedish, Korean
Table 6-5: Imaging Processing and Presentation
Image Archive/Connectivity Software Intensive Ultrasound Imaging Platform

• Image Browser: Previewing of previous archived • Digital Beamformer
images as well as current stored patient images —Displayed Imaging Depth: Minimun Depth of
• Image Management (removable media) Field is 0.5cm (probe dependent); Maximum Depth
— Delete Selected Image of Field is 30cm (probe dependent).
— Review in Full Image Area • Continuous Dynamic Receive Focus/Aperture
• One Print (Recording) UI Keys to approved printer • Multi-Frequency/Wideband Technology
• Live Scan Save: Configure save button to save an
image during live scanning CINE Memory/Image Memory
— Archiving Format: JPEG, MPEG4/ H.264 • 250MB Standard CINE Memory (120 sec of
• Capture Area: recording at most)
— Image Area • CINE Review: frame-by-frame and loop replay
— Full Screen • Live Scan Save: Configure save button to save an
• Archiving Image Frames: image during live scanning
— Single: stores single frame while in Freeze
mode
— Multiple: stores image loops while in Live scan
mode
— Patient Information Window and Search/Create
Patient Window
— Column header sorting from Image Review
Screen by name, date, ID
— Automatic generation of patient ID
— Search by ID, First Name and Last Name
• DICOM
— DICOM store
— Worklist query
— Multi-frame DICOM
• Network Quicksave

System Data
Table 6-6: Scanning Parameters
B-Mode Color Flow Mode

• Acoustic Output • ROI Position
• Thermal Index: TI • ROI Size
• Gain • Gain
• Frequency • Scale
• CrossXBeam • Depth: 0.5-30cm, defined by the preset, probe
• Gray Map dependent
• Focus Position • Threshold
• Reverse • Sample Volume
• Harmonics: defined by the preset • Frame Average
• Depth: 0.5-30cm, defined by the preset, probe • Frequency
dependent • Steer
• TGC • Acoustic Output
• ATO level • Wall Filter
• Dynamic Range • Focus Position
• Compression • Color Map
• Rejection • Compression
• Frame Average • Invert
• SRI HD • Quantification: the amount of blood flow within ROI
• Edge Enhance
• FOV PDI-Mode
• ROI Position
M-Mode • ROI Size
• Gain • Gain
• Depth: 0.5-30cm, defined by the preset, probe • Scale
dependent • Depth: 0.5-30cm, defined by the preset, probe
• Speed dependent
• Layout • Threshold
• Gray Map • Sample Volume
• Compression • Frame Average
• Edge Enhance • Frequency
• Steer
Needle Recognition Mode • Acoustic Output
• Needle Direction • Wall Filter
• Beam Angle • Focus Position
• Needle Gain • Color Map
• Compression
• Quantification: the amount of blood flow within ROI

User Maintenance
Table 6-7: Measurements and Calculations
General Measurements Obstetrics Measurements/Calculations

• Distance • Abdominal Circumference (AC)
• Area • Amniotic Fluid Index (AFI)
• Volume • Area
• Angle • Antero-Postero Trunk Diameter and Transverse
• Open Trace Trunk Diameter (APTD-TTD)
• Heart Rate/Time • Biparietal Diameter (BPD)
• Crown Rump Length (CRL)
OB Worksheet • Estimated Fetal Weight (EFW)
• Patient Information: Fetus Number, CUA/AUA • Femur Length (FL)
Selection • Gestational Sac (GS)
• Measurement Information: AFI, AC, HC, BPD, FL • Head Circumference (HC)
• Calculation Information: EFW, EFW GP (Growth • Humerus Length (HL)
Percentile), FL/BPD, FL/AC, HC/AC, FL/HC, CI • Occipito frontal Diameter (OFD)
(Cephalic Index) • Cardio-Thoracic Area Ratio (CTAR)
• OB Graphs: Fetal Graphical Trending, Quad • Fetal Trunk Cross-Sectional Area (FTA)
views, Ultrasound and gestational age • Spine Length (SL)
• Multi-Gestational Calculations
• up to 3 fetuses
• Comparison of multiple fetus data on a graph and
a worksheet

System Data
Table 6-8: Probes
12L-SC Wide Band Linear Probe L8-18i-SC: Wide Band Linear Probe
• Applications: Peripheral Vascular, Abdominal • Applications: Peripheral Vascular, Abdominal
(GYN & Urology), Pediatric, Small Organ (breast, (GYN & Urology), Pediatric, Small Organ (breast,
testes, thyroid), Neonatal Cephalic, Conventional testes, thyroid), Neonatal Cephalic, Conventional
Musculoskeletal, Superficial Musculoskeletal, Musculoskeletal, Superficial Musculoskeletal,
Thoracic/Pleural, Intraoperative (abdominal, Thoracic/Pleural, Intraoperative (abdominal,
thoracic and peripheral), Ophthalmic, Tissue thoracic and peripheral), Tissue Biopsy/Fluid
Biopsy/Fluid Drainage, Vascular Access, Drainage, Vascular Access, Nonvascular
Nonvascular • FOV (max): 25.2mm
• FOV (max): 38.4mm • B-mode Imaging Frequency: 9.0-16.0 MHz
• B-mode Imaging Frequency: 8.0-13.0 MHz • CFM Imaging Frequency: 5.0-8.7 MHz
• CFM Imaging Frequency: 5.0-6.67 MHz • Steered Angle: +/-20
• Steered Angle: +/-20
• Biopsy Guide Available: Multi-angle, Transverse E8CS-SC: Wide Band Phased Array Convex Probe
bracket, Infinite biopsy kit • Applications: Fetal/OB, Abdominal (GYN &
Urology), Transvaginal, Tissue Biopsy/Fluid
3S-SC Wide Band Phased Array Probe Drainage
• Applications: Fetal/OB, Abdominal (GYN & • Convex Radius: 8.7 mmR
Urology), Pediatric, Neonatal Cephalic, Adult • FOV: 145°
Cephalic, Cardiac (adult & pediatric), Conventional • B-mode Imaging Frequency: 5.0-9.0 MHz
Musculoskeletal, Thoracic/Pleural, Intraoperative • CFM Imaging Frequency: 4.0-5.0 MHz
(abdominal, thoracic and peripheral), Ophthalmic, • Biopsy Guide Available: Multi-angle
Tissue Biopsy/Fluid Drainage
• FOV (max): 60°-90° 10C-SC: Wide Band Phased Array Convex Probe
• B-mode Imaging Frequency: 2.0-3.4 MHz • Applications: Abdominal (GYN & Urology),
• CFM Imaging Frequency: 1.82-3.08 MHz Pediatric, Small Organ (breast, testes, thyroid),
• Biopsy Guide Available: Multi-angle Neonatal Cephalic, Superficial Musculoskeletal,
Thoracic/Pleural, Intraoperative (abdominal,
4C-SC: Wide Band Phased Array Convex Probe thoracic and peripheral), Ophthalmic
• Applications: Fetal/OB, Abdominal (GYN & • Convex Radius: 10.0 mmR
Urology), Pediatric, Conventional Musculoskeletal, • FOV: 75°-102°
Thoracic/Pleural, Intraoperative (abdominal, • B-mode Imaging Frequency: 6.0-10.0 MHz
thoracic and peripheral), Tissue Biopsy/Fluid • CFM Imaging Frequency: 4.0-5.0 MHz
Drainage, Nonvascular
• Convex Radius: 60 mmR
• FOV (max): 35°-55°, application dependent
• B-mode Imaging Frequency: 2.5-5.0 MHz
• CFM Imaging Frequency: 2.22-3.08 MHz
• Biopsy Guide Available: Multi-angle
Table 6-9: Inputs and Outputs
• 3 USB interface on Docking Station/Cart • Wireless LAN 802.11 b/g/n by wireless card
• 1 USB interface on console • Wired LAN 10/100/1000 BaseT
• 1 SD interface on console • HDMI interface on Docking Station/Cart: resolution
• Docking Connector 1280x1024@60Hz

User Maintenance
Clinical Measurement Accuracy
Basic Measurements
The following information is intended to provide guidance to the

operator in determining the amount of variation or measurement
error that should be considered when performing clinical
measurements with this equipment. Measurement error can be
contributed by equipment limitations and improper user
technique. Be sure to follow all measurement instructions and
develop uniform measurement techniques among all operators
to minimize the potential operator error. Also, in order to detect
possible equipment malfunctions that could affect measurement
accuracy, a quality assurance (QA) plan should be established
for the equipment that includes routine accuracy checks with
tissue mimicking phantoms.
Please be advised that all distance related measurements
through tissue are dependent upon the propagation velocity of
sound within the tissue. The propagation velocity usually varies
with the type of tissue, but an average velocity for soft tissue is
assumed. This equipment is designed for, and the accuracy
statements listed on are based on, an assumed average velocity
of 1540 m/s. The percent accuracy when stated applies to the
measurement obtained (not the full scale range). Where the
accuracy is stated as a percent with a fixed value, the expected
inaccuracy is the greater of the two.

System Data
Basic Measurements (continued)
Table 6-10: System Measurements and Accuracies
Limitations
or
Measurement Units Useful Range Accuracy Conditions
Distance:
Axial mm Full Screen ±5%
Lateral mm Full Screen ±5% Linear Probes
Lateral mm Full Screen ±5% Sector Probes
Lateral mm Full Screen ±5% Convex probes
Circumference:
Ellipse mm2 Full Screen ±5%
Area:
Ellipse mm2 Full Screen ±10%
Heart Rate BPM Full Screen ±5%
Time Timeline Display ±5% M mode

User Maintenance
Doppler Sensitivity
Measurements were obtained with each transducer over a

range of fluid velocities as indicated in the following table. The
maximum detectable depth of motion was measured and
converted to round-trip sensitivity in dB corresponding to the
depth and transmit frequency. The chart below summarizes the
sensitivities for all transducers in penetration-on mode.
Table 6-11: Doppler Sensitivity Data Summary
Velocity
Probe Range (cm/s) Max Depth (cm) Frequency (MHz) Sensitivity (dB)
12L-SC L 15 7 5.00 35
M 63 7 5.00 35
H 110 7 5.00 35
3S-SC L 15 15.5 2.20 34.1
M 63 15.5 2.20 34.1
H 110 15.5 2.20 34.1
4C-SC L 15 16.2 2.20 35.64
M 63 16.2 2.20 35.64
H 110 16.2 2.20 35.64
L8-18i-SC L 15 4.00 6.67 26.68
M 63 4.00 6.67 26.68
H 110 4.00 6.67 26.68
E8CS-SC L 15 7 4.00 28
M 63 7 4.00 28
H 110 7 4.00 28
10C-SC L 15 7.5 4.00 30
M 63 7.4 4.00 29.6
H 110 7.4 4.00 29.6

Venue 50 Security
At GE we’re committed to providing technologies to help you
excel every day. The Venue 50 Ultrasound system is designed
with you, your specialty and your patients in mind offering
extraordinary image quality, easy workflow and expert tools to
help you provide the best patient care.
Since the Venue 50 is integrated into your data network, GE
wants to ensure that you are comfortable with the proactive
measures we are taking to secure the product. Below are some
activities and measures that we have performed and
implemented to help secure the Venue 50.
1. Only communication ports that are needed for the Venue 50
to operate are enabled. All other operating system
communication ports are disabled.
2. Ports remaining opened are:
• Port 104 is used for DICOM communication only.
• Ports 137, 138, 139 and 445 are used for QuickSave
communication only.
• Port 2501 is used for Gateway only.
All operating system services that are not used by the
system application software are disabled to help ensure that
the source of security vulnerabilities is minimized.
3. The operating system is locked down to prevent an operator
from loading software, opening email, or using a web
browser and introducing viruses or Trojan horses to the
system.
4. The “auto run” feature is disabled on the system. For
instance, when a SD card or USB memory stick that has a
program that runs automatically is inserted, the system will
not open or run the program.
5. Our Engineering team performs a security scan on the
Venue 50 system using the same tools that major
organizations and hospital IT organizations use to check for
vulnerabilities on their networks. Failures that are detected
during this test process are corrected as expediently as
possible and are deployed to our installed base customers.

User Maintenance
Venue 50 Security (continued)

We have worked diligently to develop a combination of the
safety measures above and the native security advantage of
Venue 50 to provide a degree of safety against Viruses, Worms,
Trojan Horses, etc., especially for a system used in a
professional hospital grade networking environment that also
typically features its own sufficient safety measures.
Finally, a few points as to why we do not use Anti-Virus software.
The main reasons for not doing so:
• Customized OS of Venue 50 is natively immune to most
viruses. Only few viruses can run on Venue 50 system.
• Every Virus scanner is constantly active in the background.
Due to the software-intensive operating system of the
Ultrasound scanner, all computing resources are required
for normal operation of this device. Anti-Virus software
activities would have a negative impact on the system
performance.
• The operating software of a medical Ultrasound system is
part of an FDA-cleared medical device that requires a
specific release process. Any update of the Anti-Virus
software would mean a change of the system software.
Such change would require an extensive release and
validation process to help ensure that the Anti-Virus update
does not have any impact on the system software
performance and stability.

Overview
Refer to Chapter 10 of the Venue 50 Service Manual for any
additional maintenance guidance.
The operator must ensure that safety inspections are performed
at least every 12 months according to the requirements of the
patient safety standard IEC 60601-1. Refer to the Service
manual, Chapter 10.
Only trained persons are allowed to perform the safety
inspections mentioned above.
Technical descriptions are available on request.
To ensure that the unit constantly operates at maximum
efficiency we recommend that the following procedures be
observed as part of the customer’s internal routine maintenance
program.
Contact the local Service Representative for parts or periodic
maintenance inspections.

User Maintenance
Inspecting the System

Examine the following on a monthly basis:
• Connectors on cables for any mechanical defects.
• Entire length of electrical and power cables for cuts or
abrasions.
• Equipment for loose or missing hardware.
• Control panel for defects.
• Casters for proper locking operation.
CAUTION To avoid electrical shock hazard, do not remove panels or

covers from console. This servicing must be performed by
qualified service personnel. Failure to do so could cause
serious injury.
Biological If any defects are observed or malfunctions occur, do not

Hazard operate the equipment but inform a qualified service person.
Contact a Service Representative for information.

Weekly Maintenance
The system requires weekly care and maintenance to function
safely and properly. Clean the following:
• Console
• Docking Station/Cart
• Printer
• Footswitch
Failure to perform required maintenance may result in
unnecessary service calls.

User Maintenance
Cleaning the system

Prior to cleaning any part of the system:
1. Turn off the system power.
LCD Monitor cleaning and sterilization
To clean the monitor face:

Use the protective bag to wipe monitor face gently.
Or
Wipe the LCD monitor with the following cleaners:
• PDI Sani-Cloth Plus Germicidal Disposable Cloth (low
Alcohol)
• PDI Super Sani-Cloth Germicidal Disposable Cloth (high
Alcohol)
• PDI Sani-Cloth HB (Germicidal, Alcohol free)
• Alcohol (concentration no more than 75%)
NOTE: DO NOT use a glass cleaner that has a hydrocarbon base (such
as Benzene, Methyl Alcohol or Methyl Ethyl Ketone) on monitors
with the filter (anti-glare shield). Hard rubbing will also damage
the filter.
NOTE: When cleaning the screen, make sure not to scratch the LCD.
Footswitch
To clean the footswitch:

1. Disconnect the footswitch from the Venue 50.
2. Moisten a soft, non-abrasive folded cloth with a mild,
general purpose, non-abrasive soap and water solution.
NOTE: The cloth should be damp, not dripping wet.
3. Wipe the external surfaces of the unit then dry with a soft,
clean, cloth.

Docking Station/Cart
To clean the Docking Station/Cart:

Use a soft, folded cloth with lukewarm water. Gently wipe the
top, front, back, and both sides of the Docking Station/Cart. Dry
with a cloth or dry in air.
Or
Wipe the Docking Station/Cart with the following cleaners:
• PDI Sani-Cloth Plus Germicidal Disposable Cloth (low
Alcohol)
• PDI Super Sani-Cloth Germicidal Disposable Cloth (high
Alcohol)
• PDI Sani-Cloth HB (Germicidal, Alcohol free)
• Alcohol (concentration no more than 75%)

User Maintenance
Printer
To clean the printer:

1. Turn off the power. If possible, disconnect the power cord.
2. Wipe the external surfaces of the unit with a soft, clean, dry
cloth.
3. Remove stubborn stains with a cloth lightly dampened with
a mild detergent solution.
NOTE: Never use strong solvents, such as thinner or benzine, or
abrasive cleansers because they will damage the cabinet.
No further maintenance, such as lubrication, is required.
To clean the surface of the print head:
1. Run the cleaning sheet (provided with the printer) through
the printer.
For more information, see the Printer's Operator Manual.

Other Maintenance
Battery Replacement and Disposition
Battery replacement every three years is recommended.

Contact a local Service Representative for the replacement of
the battery. Used batteries will be discarded appropriately by
GE.
NOTE: Disposing of the battery should meet local law and regulatory
requirements.

User Maintenance
Quality Assurance
Introduction
A good Quality Assurance Evaluation program consists of
periodic systematic actions that provide the operator with
adequate confidence that their diagnostic ultrasound system will
produce consistently high quality images and quantitative
information.
Therefore, it is in the best interest of every ultrasound operator
to routinely monitor equipment performance.
The frequency of Quality Assurance Evaluations should be
based on operator's specific needs and clinical practice.
Periodic monitoring is essential in order to detect the
performance changes that occur through normal aging of
system components. Routine equipment evaluations may also
reduce the duration of exams, number of repeat exams, and
maintenance time required.
For details on system and peripheral routine preventive
maintenance instructions, See ‘System Care and Maintenance’

Quality Assurance
Typical Tests to Perform

Quality assurance measurements provide results relating to
system performance. Typically these are:
• Axial Measurement Accuracy
• Lateral Measurement Accuracy
• Axial and Lateral Resolution
• Penetration
• Functional & Contrast Resolution
• Gray Scale Photography
With these tests, a performance baseline can be set at
installation with the phantom in your department. Future test
results can be compared to the baseline in order to maintain a
record of system performance trends.
The phantom shown is shown as a representative example of a
phantom. You can select from any number of phantoms
available on the market.
Frequency of tests
Quality assurance tests are used to determine whether a

scanner is providing the same level of performance from day to
day.
The frequency of testing varies with the amount of system usage
and modes to be tested. It is recommended that the operator
perform quality assurance tests at least every three months or
every 400 patient studies. Tests should also be performed when
a question about system performance exists.
A mobile system may require more frequent tests.
Image quality should also be tested immediately after the
following events:
• Service calls
• System upgrades/modifications
• Dropped probe, power surge, etc.

User Maintenance
Phantoms
Quality Assurance Evaluations should be done with phantoms

and test objects that are applicable to the parameters being
evaluated or to the operator's clinical practice.
Typical phantoms are composed of material that acoustically
mimic human tissue. Pins, anechoic and echogenic targets are
physically positioned to provide information for a variety of tests.
The RMI 403GS phantom is shown in the illustration below as a
representative example of a phantom.
Figure 6-1. Phantoms
1. Penetration
2. Axial Distance Measurement
3. Functional Resolution
4. Lateral Resolution
5. Lateral Distance Measurement
6. Axial Resolution
7. Contrast Resolution
8. Gray Scale Plane Targets

Quality Assurance
Baselines
An absolute necessity for a quality assurance program is
establishing baselines for each test or check. Baselines are
established after the system has been verified to be working
properly at installation or after a repair. If a probe or major
assembly is replaced, new baselines should be generated.
Baselines can be made by adjusting system parameters to
prescribed levels or to the best possible image. The key factor to
remember is reproducibility. The same conditions must be
reproduced for each periodic check.
All system parameters not displayed on the monitor should be
recorded for the permanent record.
Periodic Checks
Periodic checks should be performed in accordance with your
facility’s quality assurance requirements. For the data to be
valid, periodic checks should mimic the baseline setup
parameters.
The resulting image, when scanning the phantom exactly as
before, should be recorded and compared to the baseline.
When a matching image is obtained, it can be assumed that the
system performance has not degraded from the baseline.
If a significant difference between the baseline and periodic
check is noted, double check the system setup and repeat the
test. If the difference between the baseline and periodic check
persists, contact a local Service Representative.
Failing to reproduce the control settings as in the baselines will
introduce errors in the data and potentially invalidate the results.

User Maintenance
Results
Lack of standardization among test instruments, the wide range
of acceptance criteria, and incomplete knowledge regarding the
significance of certain performance parameters prohibit the
establishment of absolute performance criteria for these tests.
Quality Assurance Evaluation results should be compared to
previously-recorded results.
Performance trends can then be detected. Unacceptable
performance or diminishing trends should be identified for
maintenance or repair before a malfunction or inappropriate
diagnosis occurs.
The operator should determine the best method for recording
and archiving the baseline and periodic checks. In most cases
the choice is hard copy.
It is important to maintain good consistent records for
inspections that may arise, as well as to detect system
performance trends.

Quality Assurance
System Setup
The operator should tailor the tests to their particular needs. It is
certainly not necessary to make all checks with all probes. A
representative example, with the probes used most often by the
customer, should be adequate in judging system performance
trends.
Use a gray scale phantom as the scan object for the tests.
Commercial phantoms are supplied with its own operator
manual. Be familiar with proper phantom operating procedures
prior to use for quality assurance evaluations.
1. Adjust image monitor. Brightness and contrast should be set
to the normal viewing of a good gray scale image.
2. Check all recording devices for proper duplication of image
monitor. Ensure that what is seen is what is recorded.
3. Annotate non-displayed image processing controls.
4. Set TGC to center position.
5. Place focal zone marker(s) in area of interest for an
optimum image.
Test Procedures
The following are recommended Quality Assurance tests. A brief
description of the test, the benefit it provides and steps to
accomplish the test are supplied.
The importance of recording scan parameters and consistent
record keeping cannot be stressed enough. Reproducibility to
monitor system trends is the key to quality assurance
evaluations.

User Maintenance
Axial distance measurements
Description
Axial measurements are the distance measurements obtained
along the sound beam. See Figure 6-1 for more information.
Benefit
The accurate measurement of a structure is a critical factor in
determining a proper diagnosis. Most imaging systems use
depth markers and/or electronic calipers for this purpose.
Method
Axial distance should be measured in the near, mid and far fields
as well as in zoom. If necessary, different depths or fields of
view can be tested.
Procedure
To measure axial distance:
1. Scan a test phantom with precisely-spaced vertical pin
targets. Adjust all scan controls, as necessary, for the best
image of the pin targets to typical depths for the probe being
used.
2. Press Freeze to stop image acquisition and perform a
standard distance measurement between the pins at
different points in the image. Record all images for
archiving.
3. Scan the vertical pins in zoom or at different depth/scale
factors.
4. Press Freeze to stop image acquisition; repeat the distance
measurements between pins and record the images for
archiving.
5. Document the measurements for reference and future
comparison.
Contact a Service Engineer if vertical measurements differ by
more than 5% of the actual distance.

Quality Assurance
Lateral distance measurements
Description
Lateral measurements are distance measurements obtained
perpendicular to the axis of the sound beam. See Figure 6-1 for
more information.
Benefit
The purpose is the same as vertical measurements.
Precisely-spaced horizontal pin targets are scanned and results
compared to the known distance in the phantom.
Method
Lateral distance should be measured in the near, mid and far
fields as well as in zoom. If necessary, different depths of fields
of view can be tested.
Procedure
To measure lateral distance:
1. Scan a test phantom with precisely-spaced horizontal pin
targets. Adjust all scan controls, as necessary, for the best
image of the pin targets from side to side.
standard distance measurement between the pins at
different points in the image. Record all images for
archiving.
3. Scan the horizontal pins in zoom or at different depth/scale
factors.
4. Press Freeze to stop image acquisition; repeat the distance
measurements between pins and record the images for
archiving.
comparison.
Contact a Service Engineer if horizontal measurements differ by
more than 5% of that depth, whichever is greater.

User Maintenance
Axial resolution
Description
Axial resolution is the minimum reflector separation between two
closely-spaced objects to produce discrete reflections along the
axis of the sound beam. It can also be monitored by checking
the vertical size of known pin targets. See Figure 6-1 for more
information.
Axial resolution is affected by the transmitting section of the
system and the probe.
Benefit
In clinical imaging, poor axial resolution displays small
structures lying close together as a single dot. This may lead to
improper interpretation of the ultrasound image.
Procedure
To measure Axial resolution:
1. Scan a test phantom with precisely-spaced vertical pin
targets.
2. Adjust all scan controls, as necessary, for the best image of
the pin targets to typical depths for the probe being used.
3. Press Freeze to stop image acquisition.
4. Perform a standard distance measurement of the pin
vertical thickness at different points in the image. Record all
images for archiving.
5. Scan the vertical pins in zoom or at different depth/scale
factors.
6. Press Freeze to stop image acquisition; repeat the vertical
thickness measurements of the pins and record the images
for archiving.
comparison.
Axial resolution should remain stable over time. Contact a
Service Engineer if any changes are observed.

Quality Assurance
Lateral resolution
Description
Lateral resolution is the minimum reflector separation between
two closely spaced objects to produce discrete reflections
perpendicular to the axis of the sound beam. It can also be
monitored by checking the horizontal size of known pin targets.
See Figure 6-1 for more information.
Lateral resolution is dependent upon the beam width produced
by the probe. The narrower the beam, the better the lateral
resolution.
The beam width is affected by the frequency, degree of focusing,
and distance of the object from the face of the probe.
Benefit
Clinically, poor lateral resolution will display small structures
lying close together as a single dot. This may lead to improper
interpretation of the ultrasound image.
Procedure
To measure lateral resolution:
1. Scan a test phantom with precisely-spaced horizontal pin
targets.
2. Adjust all scan controls, as necessary, for the best image of
the pin targets from side to side.
standard distance measurement of the horizontal thickness
of a pin at different points in the image. Record all images
for archiving.
4. Scan the horizontal pins in zoom or at different depth/scale
factors.
5. Press Freeze to stop image acquisition; repeat the
horizontal thickness measurements of the pins and record
the images for archiving.
comparison.
Pin width should remain relatively constant over time ("1mm).
Dramatic changes in pin width may indicate beamforming
problems. Contact a Service Engineer if beam width changes
consistently over 2 to 3 periodic tests.

User Maintenance
Penetration
Description
Penetration is the ability of an imaging system to detect and
display weak echoes from small objects at large depths. See
Figure 6-1 for more information.
Penetration can be affected by the system's:
• Transmitter/receiver
• Degree of probe focusing
• Attenuation of the medium
• Depth and shape of reflecting object
• Electromagnetic interference from local surroundings.
Benefit
Weak reflecting echoes are commonly produced from the
internal structure of organs. Definition of this tissue texture is
important in the interpretation of the ultrasound findings.
Method
Scan a phantom to see how echoes begin to fade as depth is
increased. The maximum depth of penetration is the point at
which homogeneous material in the phantom begins to lose
brightness.
Procedure
To measure penetration:
2. Gain and acoustic output can be adjusted, as necessary,
since these values are displayed on the monitor.
3. Scan a test phantom along the vertical pin targets to typical
depths for the probe being used.
4. Perform a standard distance measurement from the top of
the image displayed to the point at which homogeneous
material in the phantom begins to lose brightness.
5. Document the depth measurement for reference and future
comparison.
Contact a Service Engineer if the depth of penetration shifts
more than one centimeter (1cm) when using the same probe
and same system settings.

Quality Assurance
Functional resolution
Description
Functional resolution is an imaging system's ability to detect and
display the size, shape, and depth of an anechoic structure, as
opposed to a pin target. See Figure 6-1 for more information.
The very best possible image is somewhat less important than
reproducibility and stability over time. Routine tests at the same
settings should produce the same results.
Benefit
The data obtained will give a relative indication of the smallest
structure the system is capable of resolving at a given depth.
Procedure
To measure functional resolution:
2. Gain and acoustic output can be adjusted as necessary,
3. Scan a test phantom with a vertical row of anechoic cyst
targets to typical depths for the probe being used.
4. Evaluate the cysts at various depths for a good (round)
shape, well-defined borders and no fill in.
5. Document all results for future reference and comparison.
Contact a Service Engineer if a greatly distorted image is
obtained.

User Maintenance
Contrast resolution
Description
Contrast resolution is the ability of an imaging system to detect
and display the shape and echogenic characteristics of a
structure. See Figure 6-1 for more information.
Specific values measured are less important than stability over
time. Routine tests at the same settings should produce the
same results.
Benefit
A correct diagnosis is dependent upon an imaging system's
ability to differentiate between a cystic or solid structure versus
echo patterns from normal surrounding tissue.
Method
A phantom with echogenic targets of different sizes and depths
should be used.
Procedure
To measure contrast resolution:
2. Gain and acoustic output can be adjusted, as necessary,
3. Scan a test phantom with echogenic targets at the depths
available.
4. Evaluate the echogenic targets for contrast between each
other and between the surrounding phantom material.
Contact a Service Engineer if the echogenic characteristics or
shapes of the targets appear distorted.

Quality Assurance
Gray Scale photography
Description
Poor photography will cause loss of low level echoes and the
lack of contrast between large amplitude echoes. See
Figure 6-1 for more information.
Benefit
When photographic controls and film processors are properly
adjusted, weak echoes, as well as strong echoes, are accurately
recorded on film.
Procedure
1. Adjust the camera according to the manufacturer's
instructions until the hard copy and video display are equal.
2. Scan the phantom and it's echogenic contrast targets.
3. Make a hard copy photograph of the display and compare it
to the image on the video monitor for contrast and weak
echo display.
Contact a Service Engineer if camera cannot duplicate what is
on the image monitor.
NOTE: Optimization of brightness/contrast controls on the display
monitor is imperative in order to make sure that the hardcopy
and monitor look alike.
The display monitor is adjusted first. The hardcopy camera or
printer is adjusted to match the display monitor.

User Maintenance
Setting up a Record Keeping System
Preparation
The following is needed:

• Quality Assurance binder
• Hard copy or electronic file of images
• Quality Assurance checklists
• Display the following information while testing quality
assurance:
• Acoustic Output
• Gain
• Depth
• Probe
• Set up new patient to be the name of the test
• Annotate the following:
• Any control where its value is NOT displayed
• Significant phantom information
Record Keeping
Complete the following:

1. Fill out the Ultrasound Quality Assurance checklist for each
probe, as scheduled.
2. Make a hard copy or archive the image.
3. Compare images to baseline images and acceptable
values.
4. Evaluate trends over previous test periods.
5. File hard copy or electronic file of images and checklist in
Quality Assurance binder.

Quality Assurance
Ultrasound Quality Assurance Checklist

Table 6-12: Ultrasound Quality Assurance Checklist (Part 1)
Performed By Date
System Serial Number
Probe Type Probe Model Serial Number
Phantom Model Serial Number Room Temperature
Acoustic Output Gain Focal Zone
Gray Map TGC Depth
Monitor Setting
Peripheral Settings
Other Image Processing Control Settings
Table 6-13: Ultrasound Quality Assurance Checklist (Part 2)
Baseline Image Service

Value Tested Hardcopy/ Acceptable? Called Date
Test Range Value Archived Yes/No (Date) Resolved
Vertical
Measurement
Accuracy
Horizontal
Measurement
Accuracy
Axial
Resolution
Lateral
Resolution
Penetration
Functional
Resolution
Contrast
Resolution
Gray Scale
Photography
NOTE: This is an example checklist, not all the items are available for
Venue 50.

User Maintenance
CAUTION DO NOT connect any probes or accessories without approval

by GE.
Not all features, products, probes or peripherals described in

this document may be available or cleared for sale in all
markets.
Contact the distributor, GE affiliate or sales representative for
approved peripherals. For HCATs, contact your sales person.
The following supplies/accessories have been verified to be
compatible with the system:
Peripherals
Table 6-14: Peripherals and Accessories
Accessory Unit
Sony Digital Graphic Printer (UP-D897) Each
SDHC Card (Kingston 8GB SDHC Class 10 Flash Card V) Each
SD Card Reader (Transcend Compact Card Reader TS-RDP5K) Each
USB Memory Stick (SanDisk Cruzer Micro 4GB Flash Drive) Each
Edimax Wireless Adapter EW-7711UTn Each
Barcode Reader (Honeywell Corded Area-Imaging Scanner Xenon 1900) Each
Footswitch (Steute MKF 2 1S/1S-MED HID GP26) Each

Console
Table 6-15: Console Accessories
Accessory Units
Battery Pack model (NZBP32) Each
3-probe Port Each
Docking Station Each
Docking Cart Each
Probes
Table 6-16: Probes and Accessories
Accessory Units
3S-SC Each
12L-SC Each
4C-SC Each
L8-18i-SC Each
E8CS-SC Each
10C-SC Each
3S-SC biospy kit Each
12L-SC biospy kit Each
4C-SC biospy kit Each
E8CS-SC biospy kit Each
Gel
Table 6-17: Gel
Accessory Units
Aquasonic 100 Scan Gel 5 liter jug
250 ml plastic bottles (12/

case)

User Maintenance
Contact Information
Contacting GE Ultrasound
For additional information or assistance, please contact your
local distributor or the appropriate support resource listed on the
following pages:
INTERNET http://www.gehealthcare.com
http://www.gehealthcare.com/usen/ultrasound/products/
probe_care.html
Clinical Questions For information in the United States, Canada, Mexico and parts
of the Caribbean, call the Customer Answer Center.
TEL: (1) 800-682-5327 or (1) 262-524-5698
In other locations, contact your local Applications, Sales, or
Service Representative.
Service Questions For service in the United States, call GE CARES.
TEL: (1) 800-437-1171
In other locations, contact your local Service Representative.
Information To request technical product information in the United States,
Requests call GE.
TEL: (1) 800-643-6439
Placing an Order To order accessories, supplies, or service parts in the United
States, call the GE Technologies Contact Center.
TEL: (1) 800-558-5102

Contact Information
Contacting GE Ultrasound (continued)
AMERICAS
ARGENTINA GEME S.A.

Miranda 5237
Buenos Aires - 1407
TEL: (1) 639-1619 FAX: (1) 567-2678
BRAZIL GE Healthcare do Brasil Comércio e Serviços para

Equipamentos Médico- Hospitalares Ltda
Av. Das Nações Unidas, 8501
3º andar parte - Pinheiros
São Paulo SP – CEP: 05425-070
C.N.P.J.: 02.029.372/0001-40
TEL: 3067-8010 FAX: (011) 3067-8280
CANADA Ultrasound Service Engineering

9900 Innovation Drive
Wauwatosa, WI 53226
TEL: (1) 800-668-0732
Customer Answer Center TEL: (1) 262-524-5698
LATIN & SOUTH Ultrasound Service Engineering

AMERICA 9900 Innovation Drive
Wauwatosa, WI 53226
TEL: (1) 262-524-5300
Customer Answer Center TEL: (1) 262-524-5698
MEXICO GE Sistemas Medicos de Mexico S.A. de C.V.

Rio Lerma #302, 1° y 2° Pisos
Colonia Cuauhtemoc
06500-Mexico, D.F.
TEL: (5) 228-9600 FAX: (5) 211-4631
USA Ultrasound Service Engineering

9900 Innovation Drive
Wauwatosa, WI 53226
TEL: (1) 800-437-1171 FAX: (1) 414-721-3865

User Maintenance
ASIA
ASIA PACIFIC GE Healthcare Asia Pacific

JAPAN 4-7-127, Asahigaoka
Hinoshi, Tokyo
191-8503, Japan
TEL: +81 42 585 5111
AUSTRALIA Building 4B, 21 South St

Rydalmere NSW 2116
Australia
TEL: 1300 722 229
CHINA GE Healthcare - Asia

No. 1, Yongchang North Road
Beijing Economic & Technology Development Area
Beijing 100176, China
TEL: (8610) 5806 8888 FAX: (8610) 6787 1162
INDIA Wipro GE Healthcare Pvt Ltd

No. 4, Kadugodi Industrial Area
Bangalore, 560067
TEL: +(91) 1-800-425-8025
KOREA 8F, POBA Gangnam Tower

343, Hakdong-ro, Gangnam-gu
Seoul 135-820, Korea
TEL: +82 2 6201 3114
NEW ZEALAND 8 Tangihua Street

Auckland 1010
New Zealand
TEL: 0800 434 325
SINGAPORE ASEAN
1 Maritime Square #13-01
HarbourFront Center
Singapore 099253
TEL: +65 6291 8528

Contact Information
EUROPE
For all other European countries not listed, please contact your
local GE distributor or the appropriate support resource listed on
www.gehealthcare.com.
AUSTRIA General Electric Austria GmbH
Filiale GE Healthcare Technologies
EURO PLAZA, Gebäude E
Wienerbergstrasse 41
A-1120 Vienna
TEL: (+43) 1 97272 0 FAX: (+43) 1 97272 2222
BELGIUM & GE Medical Systems Ultrasound

LUXEMBURG Eagle Building
Kouterveldstraat 20
1831 DIEGEM
TEL: (+32) 2 719 7204 FAX: (+32) 2 719 7205
CZECH REPUBLIC GE Medical Systems Ultrasound

Vyskocilova 1422/1a
140 28 Praha
DENMARK GE Medical Systems Ultrasound

Park Alle 295, 2605 Brøndby
TEL: (+45) 43 295 400 FAX: (+45) 43 295 399
ESTONIA & GE Medical Systems

FINLAND Kuortaneenkatu 2, 000510 Helsinki
P.O.Box 330, 00031 GE Finland
TEL: (+358) 10 39 48 220 FAX: (+358) 10 39 48 221
FRANCE GE Medical Systems Ultrasound

and Primary Care Diagnostics
F-78457 Velizy
General Imaging TEL: (+33) 13 449 52 43
Cardiology TEL: (+33) 13 449 52 31
FAX: (+33) 13 44 95 202

User Maintenance
EUROPE (continued)
GERMANY GE Healthcare GmbH

Beethovenstrasse 239
42655 Solingen
TEL: (+49) 212-28 02-0 FAX: (+49) 212-28 02 28
GREECE GE Healthcare
8-10 Sorou Str. Marousi
Athens 15125 Hellas
TEL: (+30) 210 8930600 FAX: (+30) 210 9625931
HUNGARY GE Hungary Zrt. Ultrasound

Division, Akron u. 2.
Budaors 2040 Hungary
TEL: (+36) 23 410 314 FAX: (+36) 23 410 390
IRELAND NORTHERN IRELAND

GE Healthcare
Victoria Business Park
9, Westbank Road, Belfast BT3 9JL.
TEL: (+44) 28 90229900
REPUBLIC OF IRELAND
GE Healthcare
Unit F4, Centrepoint Business Park
Oak Drive, Dublin 22
TEL: (+353) 1 4605500
ITALY GE Medical Systems Italia spa

Via Galeno, 36, 20126 Milano
TEL: (+39) 02 2600 1111 FAX: (+39) 02 2600 1599
LUXEMBORG See Belgium.
NETHERLANDS GE Healthcare
De Wel 18 B, 3871 MV Hoevelaken
PO Box 22, 3870 CA Hoevelaken
TEL: (+31) 33 254 1290 FAX: (+31) 33 254 1292

Contact Information
EUROPE (continued)
NORWAY GE Medical Systems Ultrasound

Tåsenveien 71, 0873 Oslo
TEL: (+47) 2202 0800
GE Medical Systems Ultrasound

Strandpromenaden 45
P.O. Box 141, 3191 Horten
TEL: (+47) 33 02 11 16
POLAND GE Medical Systems Polska

Sp. z o.o., ul. Woloska 9
02-583 Warszawa, Poland
TEL: (+48) 22 330 83 00 FAX: (+48) 22 330 83 83
PORTUGAL General Electric Portuguesa

SA. Avenida do Forte, n° 4
Fraccao F, 2795-502 Carnaxide
TEL: (+351) 21 425 1309 FAX: (+351) 21 425 1343
RUSSIA GE Healthcare
Krasnopresnenskaya nab.
18, bld A, 10th floor
123317 Moscow, Russia
TEL: (+7) 4957 396931 FAX: (+7) 4957 396932
SPAIN GE Healthcare Espana

C/ Gobelas 35-37
28023 Madrid
TEL: (+34) 91 663 2500 FAX: (+34) 91 663 2501
SWEDEN GE Medical Systems Ultrasound

PO Box 314, 17175 Stockholm
TEL: (+46) 8 559 50010

User Maintenance
EUROPE (continued)
SWITZERLAND GE Medical Systems Ab

Europastrasse 31
8152 Glattbrugg
TEL: (+41) 1 809 92 92 FAX: (+41) 1 809 92 22
TURKEY GE Healthcare Türkiye

Istanbul Office
Levent Ofis
Esentepe Mah. Harman Sok.
No:8 Sisli-Istanbul
TEL: +90 212 398 07 00 FAX: +90 212 284 67 00
UNITED ARAB GE Healthcare

EMIRATES (UAE) Dubai Internet City, Building No. 18
P. O. Box # 11549, Dubai
U.A.E
TEL: (+971) 4 429 6101 or 4 429 6161
FAX: (+971) 4 429 6201
UNITED KINGDOM GE Medical Systems Ultrasound TEL: (+44) 1707 263570

71 Great North Road FAX: (+44) 1707 260065
Hatfield, Hertfordshire, AL9 5EN
Manufacturer
GE Medical System (China) Co., Ltd.

No. 19, Changjiang Road
WuXi National Hi-Tech Development Zone
Jiangsu, P.R. China 214028
TEL: +86 510 85225888; FAX: +86 510 85226688

Index
A D
accessories Danger icon, defined, 1-8
ordering, 6-38 devices
requesting a catalog, 6-38 acceptable, 1-29
accessory unapproved, 1-29
connector panel, 2-13 DICOM Image Store, 3-92
Acclimation time, 2-4 DICOM Worklist, 3-92
accuracy disinfecting probes, 5-13
clinical measurement, 6-8 disinfecting solutions, probes, 5-13
acoustic output distance measurement
default levels, 1-32 general, 3-20, 3-28
ALARA (as low as reasonably achievable), bioeffects,
1-9 E
B electrical
configurations, 2-3
biological hazards, 1-18 electrical hazard, 1-15
B-Mode measurements, mode electromagnetic compatiblity (EMC), 1-21
distance, 3-20, 3-28 EMC (electromagnetic compatiblity), 1-21
brightness, video, 2-35 Environmental requirements
probes, 5-5
C environmental requirements, 2-4
equipment safety, 1-15
Care and maintenance exam
cleaning the system, 6-16 deleting, 3-86
monitor, 6-16, 6-17
printer, 6-18 F
inspecting the system, 6-14
maintenance schedule, 6-15 Federal law (USA), requirements, 1-5
Caution icon, defined, 1-8
cleaning probes, 5-11 G
Clinical
measurement accuracy, 6-8 Gels, coupling, 5-16
console
moving, 2-22 H
transporting, 2-24
contacts hazards
biological, 5-8
clinical questions, 6-38
electrical, 5-6
Internet, 6-38
service questions, 6-38 mechanical, 5-7
hazards, safety symbols, 1-9
Control Panel
hazards, types
description, 2-41
controls biological, 1-18
electrical, 1-13, 1-15
operator, 2-41
mechanical, 1-13
heart rate, M-Mode measurements, 3-29
Venue 50 – Basic User Manual Index-1

I Q
images Quality Assurance, 6-20
deleting, 3-86 baselines, 6-23
information, requesting, 6-38 frequency of tests, 6-21
Introduction, 6-20
M periodic checks, 6-23
phantoms, 6-22
M-Mode measurements, mode record keeping, 6-34
heart rate, 3-29 system setup, 6-25
Monitor, 6-16, 6-17 test descriptions, 6-25
moving the system, 2-21 typical tests, 6-21
during transport, 2-24
precautions, 2-22 R
N Record keeping, 6-34
Network QuikSave, 3-92 S

new patient
scanning, 3-7 safety
electromagnetic compatiblity (EMC), 1-21
P equipment, 1-15
hazards, 1-9, 1-15, 1-18, 1-32, 5-6, 5-7, 5-8
patient data patient, 1-11
deleting, 3-86 acoustic output hazard
patient safety, 1-11 hazard, types
peripherals acoustic output, 1-14
connector panel, 2-13 electrical hazards, 1-13
Phantoms, 6-22 mechanical hazards, 1-13
Power, 2-27 patient identification, 1-11
connection patient training, ALARA, 1-14
USA, 2-27 personnel, 1-15
Cord, 2-21 precaution icons, defined, 1-8
OnsolOff Standby, 2-29 precaution levels, defined, 1-8
switch, location, 2-29 probes, 5-6
prescription device, caution, 1-5 handling precautions, 5-10
presets, overview, 4-2 service, requesting, 6-38
Probe handling and infection control, 5-10 site requirements, before the system arrives, 2-3
Probes System
connecting, 2-37 acclimation time, 2-4
probes system
cable handling, 2-38, 5-2 electrical configurations, 2-3
care and maintenance, 5-5 environmental requirements, 2-4
cleaning, 5-11
coupling gels W
coupling gels, probes, 5-16
deactivating, 2-38 Warning icon, defined, 1-8
disconnecting, 2-39
disinfecting, 5-13
environmental requirements, 5-5
ergonomics, 5-2
planned maintenance, 5-17
probe orientation, 5-3
safety, 5-6
using protective sheaths, 5-8
storing, 2-40
transporting, 2-40
prudent use, 1-8
Index-2 Venue 50 – Basic User Manual


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Technical Publications

Direction 5446729-100 English

Venue 50 Basic User Manual

Venue 50 complies with regulatory requirements of the following European

GE Ultraschall Deutschland GmbH & Co. KG

Rev.1 2013/01/04 Initial Release

Rev.2 2013/05/21 Update UI and software functions

Rev.3 2013/09/17 Update UI and software functions

Rev.4 2013/12/12 Update UI and software functions

Rev.5 2014/01/13 Update UI

Rev.6 2014/03/13 Remove “NOTE: 10C-SC is not available in U.S.”

Rev.7 2014/09/05 Software updated

List of Effective Pages

Title Page Rev. 7 Chapter 3 Rev. 7

Revision History Rev. 7 Chapter 4 Rev. 7

Regulatory Requirements Rev. 7 Chapter 5 Rev. 7

Table of Contents Rev. 7 Chapter 6 Rev. 7

Chapter 1 Rev. 7 Index Rev. 7

Venue 50 – Basic User Manual i-1

i-2 Venue 50 – Basic User Manual

Venue 50 – Basic User Manual i-3

i-4 Venue 50 – Basic User Manual

Country Specific Approval

Venue 50 – Basic User Manual i-5

Conformance Standards - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-3

Venue 50 – Basic User Manual i-7

i-8 Venue 50 – Basic User Manual

Venue 50 – Basic User Manual i-9

i-10 Venue 50 – Basic User Manual

Venue 50 – Basic User Manual i-11

This chapter consists of information concerning

Venue 50 – Basic User Manual 1-1

1-2 Venue 50 – Basic User Manual

CAUTION Safety instructions must be reviewed before operating the unit.

Venue 50 documentation consists of various manuals:

Venue 50 – Basic User Manual 1-3

1-4 Venue 50 – Basic User Manual

Indications for Use

WARNING To avoid injury to the patient, select the Ophthalmic or Orbits

CAUTION This machine should be used in compliance with law. Some

Venue 50 – Basic User Manual 1-5

CAUTION For USA only:

1-6 Venue 50 – Basic User Manual

Notice against user modification

Venue 50 – Basic User Manual 1-7

Various levels of safety precautions may be found on the

DANGER Indicates that a specific hazard is known to exist which through

WARNING Indicates that a specific hazard is known to exist which through

CAUTION Indicates that a potential hazard may exist which through

NOTE: Indicates precautions or recommendations that should be used

1-8 Venue 50 – Basic User Manual

Potential hazards are indicated by the following icons:

Table 1-1: Potential Hazards

Icon Potential Hazard Usage Source

Biological Hazard • Cleaning and care ISO 7000

Electrical Hazard • Probes

Moving Hazard • Moving

Acoustic Output Hazard • ALARA, the use of

Explosion Hazard • Flammable anesthetic

Fire and Smoke Hazard • Replacing fuses