GE Venue Go Basic Service Manual_SM_5813707-100_2 Venue Go Service Manual Direction Number: 5813707-100 Revision: 2

PRELIMINARY

Technical Publication

Venue Go Service Manual

14.MAR.2019
GEHC_FRNT_CVR.FM

Direction Number: 5813707-100 Revision: 2

Operating Documentation

©2018 General Electric Company.

PRELIMINARY

14.MAR.2019
GEHC_FRNT_CVR.FM

© 2018 General Electric Company.

Manufacturer:

GE Medical Systems
Ultrasound & Primary Care Diagnostic LLC
9900 Innovation Drive
Wauwatosa, WI 53226
USA

PRELIMINARY

DIRECTION 5813707-100, REVISION 2 VENUE™ SERVICE MANUAL

Table of Contents

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 1

Purpose of Chapter 1 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 1

Service Manual Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 2

Contents in this Service Manual . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 2

Venue Go™ Models Covered in this Manual . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 3

Product Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 4

Important Conventions. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 6

Conventions Used in this Manual . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 6

Standard Hazard Icons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 7

Safety Considerations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 9

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 9

Human Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 9

Mechanical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 12

Electrical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 14

Venue Go™ Battery Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 17

Patient Data Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 17

Dangerous Procedure Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 18

Lockout/Tagout (LOTO) Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 19

Product Labels and Icons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 20

Universal Product Labels . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 20

Label Descriptions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 21

Venue Go™ Cart Labels Location . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 26

Returning/Shipping Probes and Repair Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 27

EMC, EMI, and ESD . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 28

Electromagnetic Compatibility (EMC) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 28

Peripherals used in the patient environment . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 28

Compliance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 29

Electrostatic Discharge (ESD) Prevention . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 30

General Caution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 30

Customer Assistance . . . . . . . . . . . . . . . . . . . . . .

Table of Contents 3

. . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 31

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Contact Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 31

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 1

Purpose of Chapter 2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 1

Console Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2

Unit Environmental Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2

Cooling Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2

Lighting Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2

Time and Manpower Requirements. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2

Electrical Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 3

EMI Limitations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 4

EMI Prevention/Abatement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 5

Probe Environmental Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 5

Time and Manpower Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 6

Facility Needs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 7

Purchaser Responsibilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 7

Required Facility Needs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 8

Networking Pre-Installation Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 12

Connectivity Installation Worksheet . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 13

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

Purpose of Chapter 3 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 1

Setup Reminders . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 2

Average Setup Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 2

Setup Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 2

Safety Reminders . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 3

Receiving and Unpacking the Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 4

Warnings for Receiving and Unpacking the Equipment . . . . . . . . . . . . . . . . . . . 3 - 4

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 4

Unpacking Venue Go™ System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 5

Unpacking Venue Go™ Cart . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 7

Physical Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 10

EMI Protection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 10

Preparing for Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 11

Verifying Customer Order . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 11

Physical Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 11

Component Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 11

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Completing the Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 15

Purpose of this Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 15

System Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 15

Electrical Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 16

Connections on the I/O Rear Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 16

Connecting Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 18

Power on/Boot up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 20

Power Shut Down . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 20

Complete Power Down . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 20

Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 21

Purpose of this Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 21

Venue Go™ Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 21

Service Screen Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 34

Optional Peripherals/Peripheral Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 35

Software Options Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 39

Connectivity Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 40

Physical Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 40

Stand-alone Venue Go™ . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 40

Wired Ethernet from Venue Go™ to a Workstation . . . . . . . . . . . . . . . . . . . . 3 - 40

Wireless Connection from Venue Go™ to a Workstation/DICOM Server . . . 3 - 40

Connectivity Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 41

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 41

Select TCP/IP Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 42

Changing the AE Title and/or Port Number (Port No.) . . . . . . . . . . . . . . . . . . . 3 - 43

Setup Connection to a DICOM server . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 43

Export Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 51

Query/Retrieve (Q/R) Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 53

Wireless Network Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 57

Disk Management Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 58

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 58

Select Destination Device . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 58

Using Removable Media . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 58

Set Remote Path for Disk Management . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 58

Setup on the Remote Share . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 58

Configure Remote Path User on the Venue Go™ . . . . . . . . . . . . . . . . . . . . . 3 - 58

InSite ExC Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3 - 59

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 59

Network Configuration - InSite ExC . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 59

Table of Contents 5

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IRECTION 5813707-100, REVISION 2 VENUE™ SERVICE MANUAL

Prerequisites for InSite ExC Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 59

Configuring the Venue Go™ for Network InSite Checkout . . . . . . . . . . . . . . 3 - 60

Options Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 67

Software Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 67

USB Flash Card Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 67

Paperwork After Setup. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 68

Installation Acceptance Test Criteria . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 68

User’s Manual(s) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 68

Product Locator Installation Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 68

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 1

Purpose of Chapter 4 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 1

General Procedures. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 2

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 2

Power ON/Boot-up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 3

Power Shutdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 5

Logging On to the Venue Go™ as “ADM” . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 5

Service Key (Dongle, HASP) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 7

Exit to Windows Desktop from the Venue Go™ Application Software . . . . . . . 4 - 8

Data Management . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 8

Backup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 8

Deleting Patient Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 9

Transporting the Venue Go™ Ultrasound Scanner . . . . . . . . . . . . . . . . . . . . 4 - 10

Functional and Safety Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 11

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 11

Safety Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 12

Phantoms Performance Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 12

Image Quality Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 13

Probe/Connectors Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 19

Peripheral Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 20

Mechanical Functions Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 24

Functionality Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 29

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 1

Purpose of Chapter 5 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 1

General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 2

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 2

Venue Go™ Mechanical Design . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 2

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Venue Go™ System Design. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 5

Cart Interfaces . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 6

External Power Supply Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 7

Venue Go™ User Interface Components . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 7

Venue Go™ Back End (C-BEB) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 9

Back End . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 9

Compact Front End Board (C-FEB) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 11

General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 11

C-FEB Interfaces . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 11

Probe Selection Board (C-PSB) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 13

Venue Go™ Display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 14

General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 14

Display Panel and Multi-Touch (MT) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 14

Speaker . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 17

External Input/Output . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 18

System Power Distribution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 19

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 19

System Monitoring . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 20

Power Management Controller . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 21

System Power Consumption . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 21

Rechargeable Battery Pack . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 21

Cooling System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 24

General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 24

Peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 25

Internal Peripheral . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 25

External Peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 25

Software Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 26

Purpose of this Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 26

Hard Disk Partitions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 26

System Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 26

Application Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 26

Common Service Desktop . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 27

Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 27

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Connectivity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 28

Purpose of this Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 28

Venue Go™ and a DICOM Server in a Network . . . . . . . . . . . . . . . . . . . . . . . 5 - 28

InSite ExC . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 29

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 29

InSite ExC Icon . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 29

Initiating a Request for Service (RFS) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 31

InSite ExC Definitions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 34

Exiting InSite ExC . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 34

Common Service Desktop . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 35

Purpose of this Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 35

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 35

iLinq Interactive Platform Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 35

Common Service Desktop (CSD) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 36

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 1

Purpose of Chapter 6 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 1

Power Supply Adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 1

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 1

Purpose of Chapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 1

Service Safety Considerations. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 2

Gathering Troubleshooting Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 6

Purpose of this Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 6

Collect Vital System Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 6

Collect a ‘Trouble Image’ with Logs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 6

Noise Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 41

Purpose of this Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 41

Contents in this Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 41

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 41

Overview of Types of Noise . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 41

Different Power Outlet . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 43

Different System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 43

Different Location . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 43

Disconnect External Cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 43

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Using a Loaner System during Faulty System Repair . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 44

Purpose of this Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 44

Transferring data to the Loaner System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 44

Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 1

Purpose of Chapter 8 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 1

Internal Parts- Replacement Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2

Preparations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2

Batteries Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 3

Back Cover Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 5

C-PSB Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 8

Probe Lever Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 10

WiFi module Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 13

Fan Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 16

C-BEB and SSD Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 20

C-FEB Heat Sync Assembly Replacement Procedure . . . . . . . . . . . . . . . . . . . 8 - 25

C-FEB Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 28

Front Display Assembly Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . 8 - 31

Speakers Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 33

Cart Bin Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 36

Mounting / Dismounting System on Cart . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 37

Cradle Assembly Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 40

Cradle Tilt Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 42

Casters Replacement Procedure. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 45

Printer Assembly Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 46

Printer and Printer Bracket Replacement Procedure . . . . . . . . . . . . . . . . . . . . 8 - 48

Cart Tray Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 50

Cart Up/Down Handle Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . 8 - 53

ECG Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 54

Printer USB Cable Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 56

ECG USB Cable Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 58

AC/DC PSU and Split Cable Replacement Procedure . . . . . . . . . . . . . . . . . . . 8 - 60

Software Loading Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 64

Software Installation/Update Procedures - General Overview . . . . . . . . . . . . . 8 - 64

Preparation and Notes for Software Upgrade Procedure . . . . . . . . . . . . . . . . . 8 - 65

Software Installation Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 66

Software Reload/Update Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 71

Software Recovery Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 78

Functional Checks to be Performed after Replacement Procedures . . . . . . . . . . . . . . .8 - 82

General Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 82

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Submitting a Replacement Procedure Report . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 82

Functional Checks Required per Replacement Part Category . . . . . . . . . . . . 8 - 82

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 1

Purpose of Chapter 9. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 1

List of Abbreviations. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 2

Venue-Go™ System on Cart Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 3

Renewal Parts Lists and Diagrams . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 4

Mechanical Hardware Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 4

Covers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 5

System Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 5

Cart Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 8

Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 10

Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 12

Software Media . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 12

System Power Cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 13

Peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 15

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 1

Periodic Maintenance Inspections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 1

Purpose of Chapter 10 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 1

Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 2

Why Perform Maintenance Procedures? . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 3

Keeping Records . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 3

Quality Assurance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 3

Maintenance Task Schedule . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 3

Tools Required. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 5

Tools Required for Servicing the Venue Go™ . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 5

System Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 6

Preliminary Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 6

Functional Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 7

Physical Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 9

Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 10

Probe Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 12

Probe Related Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 12

Probe Handling . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 12

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Basic Probe Care . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 12

Probe Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 13

Returning and Shipping of Defective Probes . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 14

Using a Test Phantom . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 15

Electrical Safety Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 16

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 16

Safety Test Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 16

Outlet Test - Wiring Arrangement - USA and Canada . . . . . . . . . . . . . . . . . . 10 - 18

Grounding Continuity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 18

Ultrasound Equipment Quality Check (EQC and IQC) . . . . . . . . . . . . . . . . . . . . . . . . .10 - 20

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WARNING

(EN)

AVERTISSEMENT

(FR)

WARNUNG

(DE)

PRELIMINARY

DIRECTION 5813707-100, REVISION 2 VENUE GO™ PROPRIETARY SERVICE MANUAL

POC_PRECAUTIONS_LEGAL

Important Precautions

TRANSLATION POLICY

THIS SERVICE MANUAL IS AVAILABLE IN ENGLISH ONLY.

• IF A CUSTOMER’S SERVICE PROVIDER REQUIRES A LANGUAGE OTHER
THAN ENGLISH, IT IS THE CUSTOMER’S RESPONSIBILITY TO PROVIDE
TRANSLATION SERVICES.

• DO NOT ATTEMPT TO SERVICE THE EQUIPMENT UNLESS THIS SERVICE
MANUAL HAS BEEN CONSULTED AND IS UNDERSTOOD.

• FAILURE TO HEED THIS WARNING MAY RESULT IN INJURY TO THE SERVICE
PROVIDER, OPERATOR OR PATIENT FROM ELECTRIC SHOCK, MECHANICAL
OR OTHER HAZARDS.

CE MANUEL DE MAINTENANCE N’EST DISPONIBLE QU’EN ANGLAIS.

• SI LE TECHNICIEN DU CLIENT A BESOIN DE CE MANUEL DANS UNE AUTRE
LANGUE QUE L’ANGLAIS, C’EST AU CLIENT QU’IL INCOMBE DE LE FAIRE
TRADUIRE.

• NE PAS TENTER D’INTERVEN TION SUR LES ÉQUIPEMENTS TANT QUE LE
MANUEL SERVICE N’A PAS ÉTÉ CONSULTÉ ET COMPRIS.

• LE NON-RESPECT DE CET AVERTISSEMENT PEUT ENTRAÎNER CHEZ LE
TECHNICIEN, L’OPÉRATEUR OU LE PATIENT DES BLESSURES DUES À DES
DANGERS ÉLECTRIQUES, MÉCANIQUES OU AUTRES.

DIESES KUNDENDIENST-HANDBUCH EXISTIERT NUR IN ENGLISCHER
SPRACHE.

• FALLS EIN FREMDER KUNDENDIENST EINE ANDERE SPRACHE BENÖTIGT,
IST ES AUFGABE DES KUNDEN FÜR EINE ENTSPRECHENDE ÜBERSETZUNG
ZU SORGEN.

• VERSUCHEN SIE NICHT, DAS GERÄT ZU REPARIEREN, BEVOR DIESES
KUNDENDIENST-HANDBUCH NICHT ZU RATE GEZOGEN UND VERSTANDEN
WURDE.

• WIRD DIESE WARNUNG NICHT BEACHTET, SO KANN ES ZU VERLETZUNGEN
DES KUNDENDIENSTTECHNIKERS, DES BEDIENERS ODER DES PATIENTEN
DURCH ELEKTRISCHE SCHLÄGE, MECHANISCHE ODER SONSTIGE
GEFAHREN KOMMEN.

- i

3/14/19

AVISO

(ES)

AVVERTENZA

(IT)

PRELIMINARY

DIRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

POC_PRECAUTIONS_LEGAL

ESTE MANUAL DE SERVICIO SÓLO EXISTE EN INGLÉS.

• SI ALGÚN PROVEEDOR DE SERVICIOS AJENO A GEHC SOLICITA UN IDIOMA
QUE NO SEA EL INGLÉS, ES RESPONSABILIDAD DEL CLIENTE OFRECER UN
SERVICIO DE TRADUCCIÓN.

• NO SE DEBERÁ DAR SERVICIO TÉCNICO AL EQUIPO, SIN HABER
CONSULTADO Y COMPRENDIDO ESTE MANUAL DE SERVICIO.

• LA NO OBSERVANCIA DEL PRESENTE AVISO PUEDE DAR LUGAR A QUE EL
PROVEEDOR DE SERVICIOS, EL OPERADOR O EL PACIENTE SUFRAN
LESIONES PROVOCADAS POR CAUSAS ELÉCTRICAS, MECÁNICAS O DE
OTRA NATURALEZA.

ESTE MANUAL DE ASSISTÊNCIA TÉCNICA SÓ SE ENCONTRA DISPONÍVEL EM
INGLÊS.

• SE QUALQUER OUTRO SERVIÇO DE ASSISTÊNCIA TÉCNICA, QUE NÃO A
GEHC, SOLICITAR ESTES MANUAIS NOUTRO IDIOMA, É DA
RESPONSABILIDADE DO CLIENTE FORNECER OS SERVIÇOS DE TRADUÇÃO.

• NÃO TENTE REPARAR O EQUIPAMENTO SEM TER CONSULTADO E
COMPREENDIDO ESTE MANUAL DE ASSISTÊNCIA TÉCNICA.

• O NÃO CUMPRIMENTO DESTE AVISO PODE POR EM PERIGO A SEGURANÇA
DO TÉCNICO, OPERADOR OU PACIENTE DEVIDO A‘ CHOQUES ELÉTRICOS,
MECÂNICOS OU OUTROS.

ESTE MANUAL DE ASSISTÊNCIA ESTÁ DISPONÍVEL APENAS EM INGLÊS.

• SE QUALQUER OUTRO SERVIÇO DE ASSISTÊNCIA TÉCNICA, QUE NÃO A
GEHC, SOLICITAR ESTES MANUAIS NOUTRO IDIOMA, É DA
RESPONSABILIDADE DO CLIENTE FORNECER OS SERVIÇOS DE TRADUÇÃO.

• NÃO TENTE EFECTUAR REPARAÇÕES NO EQUIPAMENTO SEM TER
CONSULTADO E COMPREENDIDO PREVIAMENTE ESTE MANUAL.

• A INOBSERVÂNCIA DESTE AVISO PODE RESULTAR EM FERIMENTOS NO
TÉCNICO DE ASSISTÊNCIA, OPERADOR OU PACIENTE EM CONSEQUÊNCIA
DE CHOQUE ELÉCTRICO, PERIGOS DE ORIGEM MECÂNICA, BEM COMO DE
OUTROS TIPOS.

IL PRESENTE MANUALE DI MANUTENZIONE È DISPONIBILE SOLTANTO IN
INGLESE.

• SE UN ADDETTO ALLA MANUTENZIONE ESTERNO ALLA GEHC RICHIEDE IL
MANUALE IN UNA LINGUA DIVERSA, IL CLIENTE È TENUTO A PROVVEDERE
DIRETTAMENTE ALLA TRADUZIONE.

• SI PROCEDA ALLA MANUTENZIONE DELL’APPARECCHIATURA SOLO DOPO
AVER CONSULTATO IL PRESENTE MANUALE ED AVERNE COMPRESO IL
CONTENUTO.

• NON TENERE CONTO DELLA PRESENTE AVVERTENZA POTREBBE FAR
COMPIERE OPERAZIONI DA CUI DERIVINO LESIONI ALL’ADDETTO ALLA
MANUTENZIONE, ALL’UTILIZZATORE ED AL PAZIENTE PER FOLGORAZIONE
ELETTRICA, PER URTI MECCANICI OD ALTRI RISCHI.

ii -

3/14/19

HOIATUS

(ET)

VAROITUS

(FI)

PRELIMINARY

DIRECTION 5813707-100, REVISION 2 VENUE GO™ PROPRIETARY SERVICE MANUAL

POC_PRECAUTIONS_LEGAL

KÄESOLEV TEENINDUSJUHEND ON SAADAVAL AINULT INGLISE KEELES.

• KUI KLIENDITEENINDUSE OSUTAJA NÕUAB JUHENDIT INGLISE KEELEST
ERINEVAS KEELES, VASTUTAB KLIENT TÕLKETEENUSE OSUTAMISE EEST.

• ÄRGE ÜRITAGE SEADMEID TEENINDADA ENNE EELNEVALT KÄESOLEVA
TEENINDUSJUHENDIGA TUTVUMIST JA SELLEST ARU SAAMIST.

• KÄESOLEVA HOIATUSE EIRAMINE VÕIB PÕHJUSTADA TEENUSEOSUTAJA,
OPERAATORI VÕI PATSIENDI VIGASTAMIST ELEKTRILÖÖGI, MEHAANILISE
VÕI MUU OHU TAGAJÄRJEL.

TÄMÄ HUOLTO-OHJE ON SAATAVILLA VAIN ENGLANNIKSI.

• JOS ASIAKKAAN PALVELUNTARJOAJA VAATII MUUTA KUIN
ENGLANNINKIELISTÄ MATERIAALIA, TARVITTAVAN KÄÄNNÖKSEN
HANKKIMINEN ON ASIAKKAAN VASTUULLA.

• ÄLÄ YRITÄ KORJATA LAITTEISTOA ENNEN KUIN OLET VARMASTI LUKENUT
JA YMMÄRTÄNYT TÄMÄN HUOLTO-OHJEEN.

• MIKÄLI TÄTÄ VAROITUSTA EI NOUDATETA, SEURAUKSENA VOI OLLA
PALVELUNTARJOAJAN, LAITTEISTON KÄYTTÄJÄN TAI POTILAAN
VAHINGOITTUMINEN SÄHKÖISKUN, MEKAANISEN VIAN TAI MUUN
VAARATILANTEEN VUOKSI.

ΤΟ ΠΑΡΟΝ ΕΓΧΕΙΡΙΔΙΟ ΣΕΡΒΙΣ ΔΙΑΤΙΘΕΤΑΙ ΣΤΑ ΑΓΓΛΙΚΑ ΜΟΝΟ.

• ΕΑΝ ΤΟ ΑΤΟΜΟ ΠΑΡΟΧΗΣ ΣΕΡΒΙΣ ΕΝΟΣ ΠΕΛΑΤΗ ΑΠΑΙΤΕΙ ΤΟ ΠΑΡΟΝ
ΕΓΧΕΙΡΙΔΙΟ ΣΕ ΓΛΩΣΣΑ ΕΚΤΟΣ ΤΩΝ ΑΓΓΛΙΚΩΝ, ΑΠΟΤΕΛΕΙ ΕΥΘΥΝΗ ΤΟΥ
ΠΕΛΑΤΗ ΝΑ ΠΑΡΕΧΕΙ ΥΠΗΡΕΣΙΕΣ ΜΕΤΑΦΡΑΣΗΣ.

• ΜΗΝ ΕΠΙΧΕΙΡΗΣΕΤΕ ΤΗΝ ΕΚΤΕΛΕΣΗ ΕΡΓΑΣΙΩΝ ΣΕΡΒΙΣ ΣΤΟΝ ΕΞΟΠΛΙΣΜΟ
ΕΚΤΟΣ ΕΑΝ ΕΧΕΤΕ ΣΥΜΒΟΥΛΕΥΤΕΙ ΚΑΙ ΕΧΕΤΕ ΚΑΤΑΝΟΗΣΕΙ ΤΟ ΠΑΡΟΝ
ΕΓΧΕΙΡΙΔΙΟ ΣΕΡΒΙΣ.

• ΕΑΝ ΔΕ ΛΑΒΕΤΕ ΥΠΟΨΗ ΤΗΝ ΠΡΟΕΙΔΟΠΟΙΗΣΗ ΑΥΤΗ, ΕΝΔΕΧΕΤΑΙ ΝΑ
ΠΡΟΚΛΗΘΕΙ ΤΡΑΥΜΑΤΙΣΜΟΣ ΣΤΟ ΑΤΟΜΟ ΠΑΡΟΧΗΣ ΣΕΡΒΙΣ, ΣΤΟ ΧΕΙΡΙΣΤΗ Ή
ΣΤΟΝ ΑΣΘΕΝΗ ΑΠΟ ΗΛΕΚΤΡΟΠΛΗΞΙΑ, ΜΗΧΑΝΙΚΟΥΣ Ή ΑΛΛΟΥΣ ΚΙΝΔΥΝΟΥΣ.

EZEN KARBANTARTÁSI KÉZIKÖNYV KIZÁRÓLAG ANGOL NYELVEN ÉRHETŐ EL.

• HA A VEVŐ SZOLGÁLTATÓJA ANGOLTÓL ELTÉRŐ NYELVRE TART IGÉNYT,
AKKOR A VEVŐ FELELŐSSÉGE A FORDÍTÁS ELKÉSZÍTTETÉSE.

• NE PRÓBÁLJA ELKEZDENI HASZNÁLNI A BERENDEZÉST, AMÍG A
KARBANTARTÁSI KÉZIKÖNYVBEN LEÍRTAKAT NEM ÉRTELMEZTÉK.

• EZEN FIGYELMEZTETÉS FIGYELMEN KÍVÜL HAGYÁSA A SZOLGÁLTATÓ,
MŰKÖDTETŐ VAGY A BETEG ÁRAMÜTÉS, MECHANIKAI VAGY EGYÉB
VESZÉLYHELYZET MIATTI SÉRÜLÉSÉT EREDMÉNYEZHETI.

- iii

3/14/19

ADVARSEL

(DA)

WAARSCHUWING

(NL)

PRELIMINARY

DIRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

POC_PRECAUTIONS_LEGAL

ÞESSI ÞJÓNUSTUHANDBÓK ER EINGÖNGU FÁANLEG Á ENSKU.

• EF ÞJÓNUSTUAÐILI VIÐSKIPTAMANNS ÞARFNAST ANNARS TUNGUMÁLS EN
ENSKU, ER ÞAÐ Á ÁBYRGÐ VIÐSKIPTAMANNS AÐ ÚTVEGA ÞÝÐINGU.

• REYNIÐ EKKI AÐ ÞJÓNUSTA TÆKIÐ NEMA EFTIR AÐ HAFA SKOÐAÐ OG
SKILIÐ ÞESSA ÞJÓNUSTUHANDBÓK.

• EF EKKI ER FARIÐ AÐ ÞESSARI VIÐVÖRUN GETUR ÞAÐ VALDIÐ MEIÐSLUM
ÞJÓNUSTUVEITANDA, STJÓRNANDA EÐA SJÚKLINGS VEGNA RAFLOSTS,
VÉLRÆNNAR EÐA ANNARRAR HÆTTU.

TENTO SERVISNÍ NÁVOD EXISTUJE POUZE V ANGLICKÉM JAZYCE.

• V PŘÍPADĚ, ŽE POSKYTOVATEL SLUŽEB ZÁKAZNÍKŮM POTŘEBUJE NÁVOD
V JINÉM JAZYCE, JE ZAJIŠTĚNÍ PŘEKLADU DO ODPOVÍDAJÍCÍHO JAZYKA
ÚKOLEM ZÁKAZNÍKA.

• NEPROVÁDĚJTE ÚDRŽBU TOHOTO ZAŘÍZENÍ, ANIŽ BYSTE SI PŘEČETLI
TENTO SERVISNÍ NÁVOD A POCHOPILI JEHO OBSAH.

• V PŘÍPADĚ NEDODRŽOVÁNÍ TÉTO VÝSTRAHY MŮŽE DOJÍT ÚRAZU
ELEKTRICKÁM PROUDEM PRACOVNÍKA POSKYTOVATELE SLUŽEB,
OBSLUŽNÉHO PERSONÁLU NEBO PACIENTŮ VLIVEM ELEKTRICKÉHOP
PROUDU, RESPEKTIVE VLIVEM K RIZIKU MECHANICKÉHO POŠKOZENÍ NEBO
JINÉMU RIZIKU.

DENNE SERVICEMANUAL FINDES KUN PÅ ENGELSK.

• HVIS EN KUNDES TEKNIKER HAR BRUG FOR ET ANDET SPROG END
ENGELSK, ER DET KUNDENS ANSVAR AT SØRGE FOR OVERSÆTTELSE.

• FORSØG IKKE AT SERVICERE UDSTYRET MEDMINDRE
DENNE SERVICEMANUAL ER BLEVET LÆST OG FORSTÅET.

• MANGLENDE OVERHOLDELSE AF DENNE ADVARSEL KAN MEDFØRE SKADE
PÅ GRUND AF ELEKTRISK, MEKANISK ELLER ANDEN FARE FOR
TEKNIKEREN, OPERATØREN ELLER PATIENTEN.

DEZE ONDERHOUDSHANDLEIDING IS ENKEL IN HET ENGELS VERKRIJGBAAR.

• ALS HET ONDERHOUDSPERSONEEL EEN ANDERE TAAL VEREIST, DAN IS DE
KLANT VERANTWOORDELIJK VOOR DE VERTALING ERVAN.

• PROBEER DE APPARATUUR NIET TE ONDERHOUDEN VOORDAT DEZE
ONDERHOUDSHANDLEIDING WERD GERAADPLEEGD EN BEGREPEN IS.

• INDIEN DEZE WAARSCHUWING NIET WORDT OPGEVOLGD, ZOU HET
ONDERHOUDSPERSONEEL, DE OPERATOR OF EEN PATIËNT GEWOND
KUNNEN RAKEN ALS GEVOLG VAN EEN ELEKTRISCHE SCHOK,
MECHANISCHE OF ANDERE GEVAREN.

iv -

3/14/19

ADVARSEL

(NO)

PRELIMINARY

DIRECTION 5813707-100, REVISION 2 VENUE GO™ PROPRIETARY SERVICE MANUAL

ŠĪ APKALPES ROKASGRĀMATA IR PIEEJAMA TIKAI ANGĻU VALODĀ.

• JA KLIENTA APKALPES SNIEDZĒJAM NEPIECIEŠAMA INFORMĀCIJA CITĀ
VALODĀ, NEVIS ANGĻU, KLIENTA PIENĀKUMS IR NODROŠINĀT TULKOŠANU.

• NEVEICIET APRĪKOJUMA APKALPI BEZ APKALPES ROKASGRĀMATAS
IZLASĪŠANAS UN SAPRAŠANAS.

• ŠĪ BRĪDINĀJUMA NEIEVĒROŠANA VAR RADĪT ELEKTRISKĀS STRĀVAS
TRIECIENA, MEHĀNISKU VAI CITU RISKU IZRAISĪTU TRAUMU APKALPES
SNIEDZĒJAM, OPERATORAM VAI PACIENTAM.

ŠIS EKSPLOATAVIMO VADOVAS YRA IŠLEISTAS TIK ANGLŲ KALBA.

• JEI KLIENTO PASLAUGŲ TEIKĖJUI REIKIA VADOVO KITA KALBA – NE ANGLŲ,
VERTIMU PASIRŪPINTI TURI KLIENTAS.

• NEMĖGINKITE ATLIKTI ĮRANGOS TECHNINĖS PRIEŽIŪROS DARBŲ, NEBENT
VADOVAUTUMĖTĖS ŠIUO EKSPLOATAVIMO VADOVU IR JĮ SUPRASTUMĖTE

• NEPAISANT ŠIO PERSPĖJIMO, PASLAUGŲ TEIKĖJAS, OPERATORIUS AR
PACIENTAS GALI BŪTI SUŽEISTAS DĖL ELEKTROS SMŪGIO, MECHANINIŲ AR
KITŲ PAVOJŲ.

POC_PRECAUTIONS_LEGAL

DENNE SERVICEHÅNDBOKEN FINNES BARE PÅ ENGELSK.

• HVIS KUNDENS SERVICELEVERANDØR TRENGER ET ANNET SPRÅK, ER DET
KUNDENS ANSVAR Å SØRGE FOR OVERSETTELSE.

• IKKE FORSØK Å REPARERE UTSTYRET UTEN AT DENNE
SERVICEHÅNDBOKEN ER LEST OG FORSTÅTT.

• MANGLENDE HENSYN TIL DENNE ADVARSELEN KAN FØRE TIL AT
SERVICELEVERANDØREN, OPERATØREN ELLER PASIENTEN SKADES PÅ
GRUNN AV ELEKTRISK STØT, MEKANISKE ELLER ANDRE FARER.

NINIEJSZY PODRĘCZNIK SERWISOWY DOSTĘPNY JEST JEDYNIE W JĘZYKU
ANGIELSKIM.

• JEŚLI FIRMA ŚWIADCZĄCA KLIENTOWI USŁUGI SERWISOWE WYMAGA
UDOSTĘPNIENIA PODRĘCZNIKA W JĘZYKU INNYM NIŻ ANGIELSKI,
OBOWIĄZEK ZAPEWNIENIA STOSOWNEGO TŁUMACZENIA SPOCZYWA NA
KLIENCIE.

• NIE PRÓBOWAĆ SERWISOWAĆ NINIEJSZEGO SPRZĘTU BEZ UPRZEDNIEGO
ZAPOZNANIA SIĘ Z PODRĘCZNIKIEM SERWISOWYM.

• NIEZASTOSOWANIE SIĘ DO TEGO OSTRZEŻENIA MOŻE GROZIĆ
OBRAŻENIAMI CIAŁA SERWISANTA, OPERATORA LUB PACJENTA W WYNIKU
PORAŻENIA PRĄDEM, URAZU MECHANICZNEGO LUB INNEGO RODZAJU
ZAGROŻEŃ.

- v

3/14/19

(BG)

ПРЕДУПРЕЖДЕНИЕ

UPOZORENJE

(SR)

PRELIMINARY

DIRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

POC_PRECAUTIONS_LEGAL

ACEST MANUAL DE SERVICE ESTE DISPONIBIL NUMAI ÎN LIMBA ENGLEZĂ.

• DACĂ UN FURNIZOR DE SERVICII PENTRU CLIENŢI NECESITĂ O ALTĂ LIMBĂ
DECÂT CEA ENGLEZĂ, ESTE DE DATORIA CLIENTULUI SĂ FURNIZEZE O
TRADUCERE.

• NU ÎNCERCAŢI SĂ REPARAŢI ECHIPAMENTUL DECÂT ULTERIOR
CONSULTĂRII ŞI ÎNŢELEGERII ACESTUI MANUAL DE SERVICE.

• IGNORAREA ACESTUI AVERTISMENT AR PUTEA DUCE LA RĂNIREA
DEPANATORULUI, OPERATORULUI SAU PACIENTULUI ÎN URMA
PERICOLELOR DE ELECTROCUTARE, MECANICE SAU DE ALTĂ NATURĂ.

ДАННОЕ РУКОВОДСТВО ПО ОБСЛУЖИВАНИЮ ПРЕДОСТАВЛЯЕТСЯ ТОЛЬКО
НА АНГЛИЙСКОМ ЯЗЫКЕ.

• ЕСЛИ СЕРВИСНОМУ ПЕРСОНАЛУ КЛИЕНТА НЕОБХОДИМО РУКОВОДСТВО
НЕ НА АНГЛИЙСКОМ ЯЗЫКЕ, КЛИЕНТУ СЛЕДУЕТ САМОСТОЯТЕЛЬНО
ОБЕСПЕЧИТЬ ПЕРЕВОД.

• ПЕРЕД ОБСЛУЖИВАНИЕМ ОБОРУДОВАНИЯ ОБЯЗАТЕЛЬНО ОБРАТИТЕСЬ
К ДАННОМУ РУКОВОДСТВУ И ПОЙМИТЕ ИЗЛОЖЕННЫЕ В НЕМ СВЕДЕНИЯ.

• НЕСОБЛЮДЕНИЕ УКАЗАННЫХ ТРЕБОВАНИЙ МОЖЕТ ПРИВЕСТИ К ТОМУ,
ЧТО СПЕЦИАЛИСТ ПО ТЕХОБСЛУЖИВАНИЮ, ОПЕРАТОР ИЛИ ПАЦИЕНТ
ПОЛУЧАТ УДАР ЗЛЕКТРИЧЕСКИМ ТОКОМ, МЕХАНИЧЕСКУЮ ТРАВМУ ИЛИ
ДРУГОЕ ПОВРЕЖДЕНИЕ.

ТОВА СЕРВИЗНО РЪКОВОДСТВО Е НАЛИЧНО САМО НА АНГЛИЙСКИ ЕЗИК.

• АКО ДОСТАВЧИКЪТ НА СЕРВИЗНИ УСЛУГИ НА КЛИЕНТ СЕ НУЖДАЕ ОТ
ЕЗИК, РАЗЛИЧЕН ОТ АНГЛИЙСКИ, ЗАДЪЛЖЕНИЕ НА КЛИЕНТА Е ДА
ПРЕДОСТАВИ ПРЕВОДАЧЕСКА УСЛУГА.

• НЕ СЕ ОПИТВАЙТЕ ДА ИЗВЪРШВАТЕ СЕРВИЗНО ОБСЛУЖВАНЕ НА ТОВА
ОБОРУДВАНЕ, ОСВЕН ВСЛУЧАЙ, ЧЕ СЕРВИЗНОТО РЪКОВОДСТВО Е
ПРОЧЕТЕНО И СЕ РАЗБИРА.

• НЕСПАЗВАНЕТО НА ТОВА ПРЕДУПРЕЖДЕНИЕ МОЖЕ ДА ДОВЕДЕ ДО
НАРАНЯВАНЕ НА ДОСТАВЧИКА НА СЕРВИЗНИ УСЛУГИ, НА ОПЕРАТОРА
ИЛИ ПАЦИЕНТА ВСЛЕДСТВИЕНА ТОКОВ УДАР, МЕХАНИЧНИ ИЛИ ДРУГИ
РИСКОВЕ.

OVAJ PRIRUČNIK ZA SERVISIRANJE DOSTUPAN JE SAMO NA ENGLESKOM
JEZIKU.

• AKO KLIJENTOV SERVISER ZAHTEVA JEZIK KOJI NIJE ENGLESKI,
ODGOVORNOST JE NA KLIJENTU DA PRUŽI USLUGE PREVOĐENJA.

• NEMOJTE POKUŠAVATI DA SERVISIRATE OPREMU AKO NISTE PROČITALI I
RAZUMELI PRIRUČNIK ZA SERVISIRANJE.

• AKO NE POŠTUJETE OVO UPOZORENJE, MOŽE DOĆI DO POVREĐIVANJA
SERVISERA, OPERATERA ILI PACIJENTA UZROKOVANOG ELEKTRIČNIM
UDAROM, MEHANIČKIM I DRUGIM OPASNOSTIMA.

vi -

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OPOZORILO

(SL)

UPOZORENJE

(HR)

UPOZORNENIE

(SK)

VARNING

(SV)

PRELIMINARY

DIRECTION 5813707-100, REVISION 2 VENUE GO™ PROPRIETARY SERVICE MANUAL

POC_PRECAUTIONS_LEGAL

TA SERVISNI PRIROČNIK JE NA VOLJO SAMO V ANGLEŠČINI.

• ČE PONUDNIK SERVISNIH STORITEV ZA STRANKO POTREBUJE NAVODILA V
DRUGEM JEZIKU, JE ZA PREVOD ODGOVORNA STRANKA SAMA.

• NE POSKUŠAJTE SERVISIRATI OPREME, NE DA BI PREJ PREBRALI IN
RAZUMELI SERVISNI PRIROČNIK.

• ČE TEGA OPOZORILA NE UPOŠTEVATE, OBSTAJA NEVARNOST
ELEKTRIČNEGA UDARA, MEHANSKIH ALI DRUGIH NEVARNOSTI IN
POSLEDIČNIH POŠKODB PONUDNIKA SERVISNIH STORITEV, UPORABNIKA
OPREME ALI PACIENTA.

OVAJ SERVISNI PRIRUČNIK DOSTUPAN JE SAMO NA ENGLESKOM JEZIKU.

• AKO KLIJENTOV SERVISER ZAHTIJEVA JEZIK KOJI NIJE ENGLESKI,
ODGOVORNOST KLIJENTA JE PRUŽITI USLUGE PREVOĐENJA.

• NEMOJTE POKUŠAVATI SERVISIRATI OPREMU AKO NISTE PROČITALI I
RAZUMJELI SERVISNI PRIRUČNIK.

• AKO NE POŠTUJETE OVO UPOZORENJE, MOŽE DOĆI DO OZLJEDE
SERVISERA, OPERATERA ILI PACIJENTA PROUZROČENE STRUJNIM
UDAROM, MEHANIČKIM I DRUGIM OPASNOSTIMA.

TÁTO SERVISNÁ PRÍRUČKA JE K DISPOZÍCII LEN V ANGLIČTINE.

• AK ZÁKAZNÍKOV POSKYTOVATEĽ SLUŽIEB VYŽADUJE INÝ JAZYK AKO
ANGLIČTINU, POSKYTNUTIE PREKLADATEĽSKÝCH SLUŽIEB JE
ZODPOVEDNOSŤOU ZÁKAZNÍKA.

• NEPOKÚŠAJTE SA VYKONÁVAŤ SERVIS ZARIADENIA SKÔR, AKO SI
NEPREČÍTATE SERVISNÚ PRÍRUČKU A NEPOROZUMIETE JEJ.

• ZANEDBANIE TOHTO UPOZORNENIA MÔŽE VYÚSTIŤ DO ZRANENIA
POSKYTOVATEĽA SLUŽIEB, OBSLUHUJÚCEJ OSOBY ALEBO PACIENTA
ELEKTRICKÝM PRÚDOM, PRÍPADNE DO MECHANICKÉHO ALEBO INÉHO
NEBEZPEČENSTVA.

DEN HÄR SERVICEHANDBOKEN FINNS BARA TILLGÄNGLIG PÅ ENGELSKA.

• OM EN KUNDS SERVICETEKNIKER HAR BEHOV AV ETT ANNAT SPRÅK ÄN
ENGELSKA ANSVARAR KUNDEN FÖR ATT TILLHANDAHÅLLA
ÖVERSÄTTNINGSTJÄNSTER.

• FÖRSÖK INTE UTFÖRA SERVICE PÅ UTRUSTNINGEN OM DU INTE HAR LÄST
OCH FÖRSTÅR DEN HÄR SERVICEHANDBOKEN.

• OM DU INTE TAR HÄNSYN TILL DEN HÄR VARNINGEN KAN DET RESULTERA I
SKADOR PÅ SERVICETEKNIKERN, OPERATÖREN ELLER PATIENTEN TILL
FÖLJD AV ELEKTRISKA STÖTAR, MEKANISKA FAROR ELLER ANDRA FAROR.

- vii

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(JA)

Traditional

Chinese

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POC_PRECAUTIONS_LEGAL

BU SERVİS KILAVUZU YALNIZCA İNGİLİZCE OLARAK SAĞLANMIŞTIR.

• EĞER MÜŞTERİ TEKNİSYENİ KILAVUZUN İNGİLİZCE DIŞINDAKİ BİR DİLDE
OLMASINI İSTERSE, KILAVUZU TERCÜME ETTİRMEK MÜŞTERİNİN
SORUMLULUĞUNDADIR.

• SERVİS KILAVUZUNU OKUYUP ANLAMADAN EKİPMANLARA MÜDAHALE
ETMEYİNİZ.

• BU UYARININ GÖZ ARDI EDİLMESİ, ELEKTRİK ÇARPMASI YA DA MEKANİK
VEYA DİĞER TÜRDEN KAZALAR SONUCUNDA TEKNİSYENİN, OPERATÖRÜN
YA DA HASTANIN YARALANMASINA YOL AÇABİLİR.

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DANGER

WARNINGWARNING

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DIRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

POC_PRECAUTIONS_LEGAL

DAMAGE IN TRANSPORTATION

All packages should be closely examined at time of delivery. If damage is apparent write “Damage In
Shipment” on ALL copies of the freight or express bill BEFORE delivery is accepted or “signed for” by
a GE representative or hospital receiving agent. Whether noted or concealed, damage MUST be
reported to the carrier immediately upon discovery, or in any event, within 14 days after receipt, and the
contents and containers held for inspection by the carrier. A transportation company will not pay a claim
for damage if an inspection is not requested within this 14 day period.

CERTIFIED ELECTRICAL CONTRACTOR STATEMENT - FOR USA ONLY

All electrical Installations that are preliminary to positioning of the equipment at the site prepared for the
equipment shall be performed by licensed electrical contractors. Other connections between pieces of
electrical equipment, calibrations and testing shall be performed by qualified GE personnel. In
performing all electrical work on these products, GE will use its own specially trained field engineers.
All of GE’s electrical work on these products will comply with the requirements of the applicable
electrical codes.

The purchaser of GE equipment shall only utilize qualified personnel (i.e., GE’s field engineers,
personnel of third-party service companies with equivalent training, or licensed electricians) to perform
electrical servicing on the equipment.

OMISSIONS & ERRORS

If there are any omissions, errors or suggestions for improving this documentation, please contact the
GE Global Documentation Group with specific information listing the system type, manual title, part
number or direction number, revision number, page number and suggestion details.

Mail the information to:

Service Documentation,

GE Medical Systems
Ultrasound & Primary Care Diagnostics LLC
9900 Innovation Drive
Wauwatosa, WI 53226
USA

GE employees should use TrackWise to report service documentation issues. These issues will then
be in the internal problem reporting tool and communicated to the writer.

SERVICE SAFETY CONSIDERATIONS

DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH, ARE PRESENT IN
THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING AND
ADJUSTING.

Use all Personal Protection Equipment (PPE) such as gloves, safety shoes, safety
glasses, and kneeling pad, to reduce the risk of injury.

For a complete review of all safety requirements, see the Chapter 1 Safety Considerations section in
the Service Manual.

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LEGAL NOTES

The contents of this publication may not be copied or duplicated in any form, in whole or in part, without
prior written permission of GE.

GE makes no representations or warranties with respect to the information herein. In addition, the
information is subject to change without notice. Every precaution has been taken in the preparation of
this document. Nevertheless, GE assumes no responsibility for errors, omissions, or any damages,
including special or consequential, resulting from the use of this information. GE will issue updates to
this information periodically, as needed. If there are any questions regarding the information contained
in this manual, please contact your GE Representative.'

TRADEMARKS

All products and their name brands are trademarks of their respective holders.

COPYRIGHTS

©by General Electric Company Inc. All Rights Reserved.

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Revision History

Revision Date Reason for change Doc ID Revision of Doc ID

1 23 October 2018 Initial Release DOC2073428 1

1 5 November 2018

2 5 December 2018 Revised Table 10-2, added safety test DOC2073428 3

2 4 March 2019 added WiFi module Replacement Procedure DOC2073428 4

Revised functional checks table in chp. 8
Revised section 4-3 - functional tests procedures

DOC2073428 2

List of Effected Pages (LOEP)

Pages Revision Pages Revision Pages Revision

added WiFi module

8-12 to 8-14

7-44 to 7-47

Replacement
Procedure

added Loaner system
procedure

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

Chapter 1

Introduction

Section 1-1 Overview

1-1-1 Purpose of Chapter 1

This chapter describes important issues related to safely servicing the Venue Go™ ultrasound scanner.
The service provider must read and understand all the information presented here before installing or
servicing a unit.

Chapter 1 - Introduction 1-1

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

Section 1-2 Service Manual Overview

This manual provides setup and service information for the Venue Go™ ultrasound scanner. The ten
chapters it contains are outlined in Table 1-1 below.

In the beginning of the manual, before Chapter 1, you will find the language policy for GE service
documentation, legal information, a revision overview and the Table of Contents (TOC).

An Index has not been included.

1-2-1 Contents in this Service Manual

The service manual is divided into ten chapters.

In the beginning of the manual, before chapter 1, you will find the language policy for GE service
documentation, legal information, a revision overview and the Table of Contents (TOC).

An Index has not been included.

Table 1-1 Contents in this Service Manual

CHP NUMBER TITLE DESCRIPTION

Chapter 1 Introduction

Chapter 2 Site Preparations

Chapter 3 System Setup

Chapter 4

Chapter 5

Chapter 6 Service Adjustments

Chapter 7 Diagnostics/Troubleshooting

Chapter 8 Replacement Procedures

Chapter 9 Renewal Parts

Chapter 10 Care and Maintenance

General Procedures and Functional
Checks

Venue Go™Components and
Function (Theory)

Contains a content summary and warnings.

Contains pre-setup requirements for the Venue Go™ ultrasound
scanner.

Contains setup procedure with an setup checklist.

Contains functional checks that must be performed as part of the
setup, or as required during servicing and periodic maintenance.

Contains block diagrams and functional explanations of the
electronic circuits.

Contains instructions on how to make any available service
adjustments to the Venue Go™ ultrasound scanner.

Provides instructions for setting up and running diagnostic,
troubleshooting and other related routines for the Venue Go™
ultrasound scanner.

Provides removal and installation procedures for replacement of
all Field Replaceable Units (FRUs).

Contains a complete list of field replaceable parts for the Venue
Go™ ultrasound scanner.

Provides periodic maintenance procedures for the Venue Go™
ultrasound scanner.

NOTE: The illustrations provided in this service manual are for illustration purposes only and are subject to

change without notice.

1-2-2 Typical Users of the Basic Service Manual

This manual is intended for the following categories of users:

• Service personnel (setup, maintenance, etc.).

• Hospital’s service personnel

• Architectural planners/installation planners (some parts of Chapter 2 -Site Preparations).

1-2 Chapter 1 - Introduction

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1-2-3 Venue Go™ Models Covered in this Manual

The Venue Go™ models documented in this manual are shown in Tab le 1 -2 below.

Table 1-2 Venue Go™ Models

Traced

PSI Group Cat No. Description PSI

Venue Go™ H45601VG Venue Go™ ultrasound imaging scanner

Code

UVENGA 24500A

GP

Code

by

Siebel

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

1-2-4 Product Description

1-2-4-1 Overview of the Venue Go™ Ultrasound Scanner

The Venue Go™ is a compact, phased, linear array ultrasound imaging scanner.
Weighing only 6 Kgs (13.22 lbs), each system is extremely versatile and, depending upon the installed
software, can be used for a variety of applications.

The system provides image generation in 2D, Color Doppler, M-Mode, Color M-Mode, PW and Tissue
Velocity imaging.

The fully digital architecture of the Venue Go™ system allows optimal usage of all scanning modes and
probe types throughout the full spectrum of operating frequencies.

Signal flows from the Probe Connector Panel to the Front End, and then over to the Back End Processor
and finally to the Touch Panel and peripherals.

System configuration is stored on the Venue Go™.

All necessary software is loaded from the hard drive on power up.

1-2-4-2 How to Turn the Scanner ON and OFF

• To turn the scanner ON see: Power on/Boot up on page 3 - 20

• To turn the scanner OFF see: Power Shut Down on page 3 - 20

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1-2-4-3 How to Check for Hardware/Software Version and Installed Options

• To verify the hardware versions on the boards:
Refer to HW Version tab.

• To check the software versions on local software on the boards:
Refer to Software Version.

• To check for installed options:
Refer to Options Setup on page 3 - 67.

Chapter 1 - Introduction 1-5

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DANGER

WARNINGWARNING

CAUTION

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

Section 1-3 Important Conventions

1-3-1 Conventions Used in this Manual

1-3-1-1 Model Designations

This manual covers the Venue Go™ ultrasound units listed in Tabl e 1 -2 on page 1-3

1-3-1-2 Icons

Pictures, or icons, are used wherever they will reinforce the printed message. The icons, labels and
conventions used on the product and in the service information are described in this chapter.

1-3-1-3 Safety Precaution Messages

Various levels of safety precaution messages may be found on the equipment and in the service
information. The different levels of concern are identified by a flag word that precedes the precautionary
message. Known or potential hazards to personal are labeled in one of three ways:

•DANGER

• WARNING

•CAUTION

When a hazard is present that can cause property damage, but has absolutely no personal injury risk,
a NOTICE is used.

DANGER IS USED TO INDICATE THE PRESENCE OF A HAZARD THAT WILL
CAUSE SEVERE PERSONAL INJURY OR DEATH OR SUBSTANTIAL
PROPERTY DAMAGE IF THE INSTRUCTIONS ARE IGNORED.

WARNING IS USED TO INDICATE THE PRESENCE OF A HAZARD THAT MAY CAUSE
SEVERE PERSONAL INJURY OR SUBSTANTIAL PROPERTY DAMAGE IF
INSTRUCTIONS ARE IGNORED.

CAUTION IS USED TO INDICATE THE PRESENCE OF A HAZARD THAT WILL OR CAN CAUSE
MINOR PERSONAL INJURY OR PROPERTY DAMAGE IF INSTRUCTIONS ARE IGNORED.
EQUIPMENT DAMAGE POSSIBLE.

NOTE: Notes are used to provide important information about an item or a procedure.

NOTE: Be sure to read the notes; the information contained in a note can often save you time or effort.

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

1-3-2 Standard Hazard Icons

Important information will always be preceded by the exclamation point contained within a triangle,
or the symbols for “Danger”, “Warning” or “Caution”, as seen throughout this chapter. In addition to text,

several different graphical icons (symbols) may be used to make you aware of specific types of hazards
that could cause harm. Even if a symbol isn’t used in this manual, it may be included for your reference.

Table 1-3 Standard Hazard Icons

ICON POTENTIAL HAZARD USAGE SOURCE

Biological Hazard

Describes precautions necessary to

prevent the risk of disease transmission

or infections.

• Patient/user infection due to contaminated
equipment.

Electrical Hazard

Describes precautions necessary to

prevent the risk of injury through electric

hazards.

• Electrical micro-shock to patient, e.g.,
ventricular

Moving Hazard

Describes precautions necessary to prevent the
risk of injury through moving or tipping hazard!

• Console, accessories or optional storage
devices that can fall on patient, user, or others.

• Collision with persons or objects may result in
injury while maneuvering or during system
transport.

• Injury to user from moving the console.

• Cleaning and care
instructions

• Sheath and glove
guidelines

Probes

• ECG, if applicable

• Connections to back panel

Moving

• Using brakes

• Transporting

ISO 7000

No. 0659

Acoustic Output Hazard

Patient injury or tissue damage from ultrasound
radiation.

Explosion Hazard

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

• Patient/user injury or adverse reaction from fire
or smoke.

• Patient/user injury from explosion and fire.

ALARA, the use of Power
Output following the ‘as low
as reasonably achievable’
principle.

Flammable anesthetic

• Replacing fuses

• Outlet guidelines

Other hazard icons make you aware of specific procedures that should be followed.

NOTE: The Venue Go™ system has no unintended or motorized moving parts that could cause pinching; all

moving parts are mechanically operated by the user.
Pay attention to move such parts carefully (e.g. articulated arm).

Chapter 1 - Introduction 1-7

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&

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

Table 1-4 Standard Icons Indicating a Special Procedure Be Used

AVOID STATIC ELECTRICITY TAG AND LOCK OUT

1-8 Chapter 1 - Introduction

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WARNINGWARNING

WARNINGWARNING

WARNINGWARNING

WARNINGWARNING

WARNINGWARNING

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

Section 1-4 Safety Considerations

1-4-1 Introduction

The following safety precautions must be observed during all phases of operation, service and repair of
this equipment. Failure to comply with these precautions or with specific warnings elsewhere in this
manual violates safety standards of design, manufacture and intended use of the equipment.

1-4-2 Human Safety

• Operating personnel must not remove the Ultrasound system covers.

• Servicing should be performed by authorized personnel only.

• Only personnel who have participated in a Venue Go™ Training Seminar are authorized to service
the equipment.

NOTE: United States law restricts this device for sale or use by or on the order of a physician.

DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH, ARE PRESENT IN
THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING AND
ADJUSTING.

IF THE COVERS ARE REMOVED FROM AN OPERATING VENUE GO™ SYSTEM, SOME
METAL SURFACES MAY BE WARM ENOUGH TO POSE A POTENTIAL HEAT HAZARD
IF TOUCHED, EVEN WHILE IN SHUT DOWN MODE.

FOR CONSOLE ULTRASOUND SYSTEMS AND FOR ULTRASOUND
SYSTEMS MOUNTED ON A DOCKING/ISOLATION CART, HAVE TWO
PEOPLE AVAILABLE TO DELIVER AND UNPACK THE ULTRASOUND
SYSTEM.

ATTEMPTS TO MOVE THE ULTRASOUND SYSTEM CONSIDERABLE

DISTANCES OR ON AN INCLINE BY ONE PERSON COULD RESULT IN
INJURY OR DAMAGE OR BOTH.

BECAUSE OF THE LIMITED ACCESS TO CABINETS AND EQUIPMENT IN THE FIELD,
PLACING PEOPLE IN AWKWARD POSITIONS, GE HAS LIMITED THE LIFTING WEIGHT
FOR ONE PERSON IN THE FIELD TO 16 KG (35 LBS). ANYTHING OVER 16 KG (35 LBS)
REQUIRES 2 PEOPLE.

HAVE TWO PEOPLE AVAILABLE TO DELIVER AND UNPACK THE VENUE GO™
SYSTEM. ATTEMPTS TO MOVE THE UNIT CONSIDERABLE DISTANCES OR ON AN
INCLINE BY ONE PERSON COULD RESULT IN INJURY OR DAMAGE OR BOTH.

USE ALL PERSONAL PROTECTION EQUIPMENT (PPE) SUCH AS GLOVES, SAFETY
SHOES, SAFETY GLASSES, AND KNEELING PAD, TO REDUCE THE RISK OF INJURY.

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WARNINGWARNING

WARNINGWARNING

WARNINGWARNING

WARNINGWARNING

WARNINGWARNING

WARNINGWARNING

WARNINGWARNING

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EXPLOSION WARNING

DO NOT OPERATE THE EQUIPMENT IN AN EXPLOSIVE ATMOSPHERE. OPERATION
OF ANY ELECTRICAL EQUIPMENT IN SUCH AN ENVIRONMENT CONSTITUTES A
DEFINITE SAFETY HAZARD.

DO NOT SUBSTITUTE PARTS OR MODIFY EQUIPMENT
BECAUSE OF THE DANGER OF INTRODUCING ADDITIONAL HAZARDS, DO NOT

INSTALL SUBSTITUTE PARTS OR PERFORM ANY UNAUTHORIZED MODIFICATION
OF THE EQUIPMENT.

FOR CONSOLE ULTRASOUND SYSTEMS AND FOR ULTRASOUND SYSTEMS
MOUNTED ON A CART,WHEN THE TOP CONSOLE IS IN ITS LOCKED POSITION, THE
GAS SHOCK IS COMPRESSED AND STORES MECHANICAL ENERGY. DURING
NORMAL OPERATION THE TOP CONSOLE, THE WEIGHT OF THE MONITOR AND THE
MECHANICAL FORCE OF THE GAS SHOCK ARE IN BALANCE. TAKE CARE IF/ WHEN
YOU ACTIVATE THIS GAS SHOCK.

PERSONAL INJURY CAN OCCUR AFTER THE PANEL IS REMOVED AND THE SHOCK
PRESSURE IS RELEASED. TAKE CARE WHEN YOU REPAIR THE ELEVATION
ASSEMBLY.

RISK OF ELECTRICAL SHOCK, ULTRASOUND SYSTEM MUST BE TURNED OFF AND
DISCONNECTED FROM POWER SOURCE. CORD MUST BE CONTROLLED AT ALL
TIMES.

WAIT FOR AT LEAST 30 SECONDS FOR CAPACITORS TO DISCHARGE AS THERE ARE
NO TEST POINTS TO VERIFY ISOLATION. THE LIGHT ON THE OP PANEL ON/OFF
BUTTON WILL TURN OFF.

ULTRASOUND SYSTEM COMPONENTS MAY BE ENERGIZED. ALWAYS REFER TO
THE ULTRASOUND SYSTEM'S SERVICE MANUAL FOR LOTO WARNINGS AND
CAUTIONS.

CAPACITORS ON ULTRASOUND SYSTEMS WITH THE SHEARWAVE OPTION CAN
AKE UP TO 5 MINUTES TO DISCHARGE.

FOR CONSOLE ULTRASOUND SYSTEMS AND FOR ULTRASOUND SYSTEMS
MOUNTED ON A CART, USE EXTREME CAUTION AS LONG AS THE ULTRASOUND
SYSTEM IS UN-STABLE, NOT RESTING ON ALL FOUR CASTERS.

FOR CONSOLE ULTRASOUND SYSTEMS AND FOR ULTRASOUND SYSTEMS
MOUNTED ON A CART, TILTING THE CONSOLE REQUIRES TWO PEOPLE IN ORDER
TO AVOID INJURY TO SERVICE PERSONNEL AND DAMAGE TO THE EQUIPMENT.

USE ALL PERSONAL PROTECTION EQUIPMENT (PPE) SUCH AS GLOVES, SAFETY
SHOES, SAFETY GLASSES, AND KNEELING PADS, TO REDUCE THE RISK OF INJURY.

1-10 Chapter 1 - Introduction

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WARNINGWARNING

CAUTION

CAUTION

CAUTION

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

BEWARE OF POSSIBLE SHARP EDGES ON ALL MECHANICAL PARTS. IF SHARP
EDGES ARE ENCOUNTERED, THE APPROPRIATE PPE SHOULD BE USED TO
REDUCE THE RISK OF INJURY.

WEAR ALL PPE INCLUDING GLOVES AS INDICATED IN THE CHEMICAL MSDS.

USE PROTECTIVE GLASSES DURING DRILLING, FILING AND DURING ALL OTHER WORK
WHERE EYES NEED PROTECTION.

USE SAFETY SHOES WHEN DOING WORK WHERE THERE IS ANY CHANCE OF FOOT
DAMAGE.

USE PROTECTIVE GLOVES WHEN DRILLING AND CUTTING.

Chapter 1 - Introduction 1-11

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WARNINGWARNING

WARNINGWARNING

DANGER

DANGER

DANGER

CAUTION

WARNINGWARNING

WARNINGWARNING

CAUTION

CAUTION

CAUTION

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

1-4-3 Mechanical Safety

WHILE THE SOFTWARE INSTALL PROCEDURE IS DESIGNED TO PRESERVE DATA,
YOU SHOULD SAVE ANY PATIENT DATA, IMAGES, SYSTEM SETUPS TO A DVD OR
HARDCOPY BEFORE DOING A SOFTWARE UPGRADE.

PRIOR TO ELEVATING SCANNER, VERIFY THAT THE MONITOR IS LOCKED IN ITS
LOWEST POSITION. VERIFY THAT THE FRONT BRAKE IS LOCKED AND THE
SCANNER IS UNABLE TO SWIVEL. VERIFY THAT THE REAR BRAKES ARE IN THE
LOCKED POSITION.

WHENEVER THE UNIT IS TO BE MOVED ALONG ANY INCLINE, USE EXTREME
CAUTION. MAKE SURE THAT THE VENUE GO™ SCANNER AND ALL PERIPHERALS
ARE SECURELY MOUNTED IN PLACE BEFORE ATTEMPTING TO MOVE IT.

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.

NEVER USE A PROBE THAT HAS FALLEN TO THE FLOOR. EVEN IF IT LOOKS OK, IT
MAY BE DAMAGED.

ULTRASOUND SYSTEM WEIGHTS CAN BE SIGNIFICANT, PLUS THE WEIGHT OF INSTALLED
PERIPHERALS, WHEN READY FOR USE. CARE MUST BE USED WHEN MOVING IT OR
REPLACING ITS PARTS.
FAILURE TO FOLLOW THE PRECAUTIONS LISTED BELOW COULD RESULT IN INJURY,
UNCONTROLLED MOTION AND COSTLY DAMAGE.

• USE THE HANDLE TO MOVE THE ULTRASOUND SYSTEM.

• BE SURE THE PATHWAY IS CLEAR. LIMIT MOVEMENT TO A SLOW CAREFUL WALK.

• DO NOT LET THE ULTRASOUND SYSTEM STRIKE WALLS OR DOOR FRAME.

• USE TWO PEOPLE WHEN MOVING ON INCLINES OR LIFTING MORE THAN 16 KG (35 LBS).

THE SYSTEM SHOULD NOT BE MOVED WITH THE OPERATING PANEL EXTENDED.
POSITION THE OPERATING PANEL IN ITS CENTERED AND LOCKED POSITION.
LOWER THE OPERATING PANEL AS MUCH AS POSSIBLE BEFORE MOVING THE
SYSTEM. See Figure 5-14 on page 5-32 illustrating system in Transportation Mode.

REMEMBER: IF THE FRONT CASTER SWIVEL LOCK IS ENGAGED FOR
TRANSPORTATION, PRESSING THE RELEASE PEDAL ONCE DISENGAGES THE
SWIVEL LOCK. YOU MUST DEPRESS THE RELEASE PEDAL A SECOND TIME TO
ENGAGE THE BRAKE.

BEFORE YOU MOVE OR TRA NSPORT THE SYSTE M, MAKE SURE T O LOCK THE LCD MONITOR
ARM FIRMLY AND FLIP DOWN THE MONITOR TO PREVENT DAMAGE TO THE SYSTEM.

See Figure 5-14 on page 5-32 illustrating system in Transportation Mode.

ALWAYS LOCK THE TOP CONSOLE (OPERATOR PANEL) IN ITS PARKING (LOCKED)
POSITION BEFORE MOVING THE SCANNER AROUND.

TO AVOID INJURY WHEN YOU MOVE THE LCD MONITOR AND THE MONITOR ARM, DO NOT PUT
YOUR FINGER, HAND, OR OBJECT ON THE JOINT OF THE MONITOR OR THE MONITOR ARM.

1-12 Chapter 1 - Introduction

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CAUTION

CAUTION

CAUTION

WARNINGWARNING

CAUTION

NOTICE

WARNINGWARNING

CAUTION

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

ENSURE THAT NO-ONE TOUCHES THE CONSOLE ARM/FROGLEG WHEN MOVING THE
OPERATOR PANEL.

DO NOT MOVE THE UNIT IF THE OPERATOR PANEL IS IN UNLOCKED POSITION.

KEEP THE HEAT VENTING HOLES ON THE MONITOR UNOBSTRUCTED TO AVOID
OVERHEATING OF THE MONITOR.

THE SYSTEM SHOULD NOT BE MOVED WITH THE OPERATING PANEL EXTENDED.
POSITION THE OPERATING PANEL IN ITS CENTERED AND LOCKED POSITION.
LOWER THE OPERATING PANEL AS MUCH AS POSSIBLE BEFORE MOVING THE
SYSTEM. See Figure 5-14 on page 5-32 illustrating system in Transportation Mode.

DO NOT TRANSPORT THE VENUE GO™ SYSTEM IN A VEHICLE WITHOUT LOCKING THE

-

-

CASTERS (WHEELS)

See Figure 5-14 ON PAGE 5-32 illustrating system in Transportation Mode.

SPECIAL CARE SHOULD BE TAKEN WHEN TRANSPORTING THE ULTRASOUND SYSTEM IN A
VEHICLE:

• BEFORE TRANSPORTING, PLACE THE ULTRASOUND SYSTEM IN ITS SPECIAL STORAGE CASE.

• ENSURE THAT THE ULTRASOUND SYSTEM IS FIRMLY SECURED WHILE INSIDE THE VEHICLE.

• SECURE ULTRASOUND SYSTEM WITH STRAPS OR AS DIRECTED OTHERWISE TO PREVENT MOTION DURING
TRANSPORT.

• PREVENT VIBRATION DAMAGE BY DRIVING CAUTIOUSLY. AVOID UNPAVED ROADS, EXCESSIVE SPEEDS, AND
ERRATIC STOPS OR STARTS.

EQUIPMENT DAMAGE COULD RESULT IF SPECIAL CARE IS NOT TAKEN WHEN
TRANSPORTING THE

VENUE GO™ SYSTEM IN A VEHICLE.

See Figure 5-14 on page 5-32 illustrating system in Transportation Mode.

ALWAYS:

• Eject any media from the media storage devices USB Flash Drive, MOD (if installed).

• Ensure that monitor is in folded and locked position.

• Ensure that the Venue Go™ system is well prepared and packed in its original packaging
before transporting. Special care must be taken to correctly position the packing material,
using all screws and brackets.
For further information, refer to Chapter 3 -System Setup.

• Place the probes in their carrying case.

• Secure the system in an full down position and lock the wheels (brake).

• Ensure that the Venue Go™ system is firmly secured while inside the vehicle.

• Secure the system with straps or as directed otherwise to prevent motion during transport.

• Prevent vibration damage by driving cautiously. Avoid unpaved roads, excessive speeds,
and erratic stops or starts.

KEEP THE HEAT VENTING HOLES ON THE MONITOR UNOBSTRUCTED TO AVOID
OVERHEATING OF THE MONITOR.

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

1-4-4 Electrical Safety

To minimize shock hazard, the equipment must be connected to a well grounded power source. The
system is equipped with a three-conductor AC power cable. This must be plugged into an approved
electrical outlet with safety grounding. To ensure proper grounding, connect this equipment to a
receptacle marked "HOSPITAL ONLY" OR "HOSPITAL GRADE".

The power outlet used for this equipment should not be shared with other types of equipment. Both the
system power cable and the power connector must meet international electrical standards.

CONNECTING A VENUE GO™ SCANNER TO INCORRECT VOLTAGE LEVEL WILL
DESTROY THE SYSTEM!!

CONNECT THE SYSTEM ONLY IN ACCORDANCE WITH THE VOLTAGE INDICATED ON
THE PRODUCT LABEL.

SAFE PRACTICES:

FOLLOW THESE GUIDELINES TO MINIMIZE SHOCK HAZARDS WHENEVER YOU ARE
USING THE ULTRASOUND SYSTEM:

• TO MINIMIZE SHOCK HAZARD, THE EQUIPMENT CHASSIS MUST BE CONNECTED TO AN ELECTRICAL GROUND.

• THE ULTRASOUND SYSTEM IS EQUIPPED WITH A THREE-CONDUCTOR AC POWER CABLE. THIS MUST BE
PLUGGED INTO AN APPROVED ELECTRICAL OUTLET WITH SAFETY GROUND.

• THE POWER OUTLET USED FOR THIS EQUIPMENT SHOULD NOT BE SHARED WITH OTHER TYPES OF EQUIPMENT.

• BOTH THE ULTRASOUND SYSTEM POWER CABLE AND THE POWER CONNECTOR MUST MEET INTERNATIONAL
ELECTRICAL STANDARDS.

1-4-4-1 Probes

All the probes for the Venue Go™ ultrasound unit are designed and manufactured to provide trouble­free, reliable service. To ensure this, correct handling of probes is important and the following points
should be noted:

• Do not drop a probe or strike it against a hard surface, as this may damage the transducer elements,
acoustic lens, or housing.

• Do not use a cracked or damaged probe. In this event, call your field service representative
immediately to obtain a replacement.

• Avoid pulling, pinching or kinking the probe cable, since a damaged cable may compromise the
electrical safety of the probe.

• To avoid the risk of a probe accidentally falling, do not allow the probe cables to become entangled,
or to be caught in the system’s wheels.

Follow these guidelines before connecting a probe to the scanner:

• Inspect the probe prior to each use for damage or degradation to the:

- housing

- cable strain relief

-lens

- seal

- connector pins

- locking mechanism

• Do not use a damaged or defective probe.

• Never immerse the probe connector or adapter into any liquid.

NOTE: For detailed information on handling endocavity probes, refer to the appropriate supplementary

instructions for each probe. In addition, refer to the Venue Go™ User Manual for detailed probe
handling instructions.

1-14 Chapter 1 - Introduction

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

1-4-4-2 Peripherals

1-4-4-2-1 Safety and Environmental Guidelines

Environmental Dangers

ALL DEVICES MEETING IEC60950 MUST BE KEPT OUTSIDE THE PATIENT
ENVIRONMENT AS DEFINED IN IEC60601-1-1, UNLESS THE DEVICES, ACCORDING TO
IEC60601-1-1, ARE EQUIPPED WITH THE FOLLOWING:

A) ADDITIONAL FIXED EARTH PROTECTION

OR:

B) AN EXTRA ISOLATING TRANSFORMER

Commercial devices such as laser cameras, printers, VCRs and external monitors,
usually exceed allowable leakage current limits and, when plugged into separate
AC outlets, are in violation of patient safety standards. Suitable electrical isolation of
such external AC outlets, or the provision of extra protective earth for the device, is
required in order to meet UL60601-1 and IEC60601-1-1 standards for electrical leakage.

• Patient Vicinity UL 60601-1
Sub clause 2.12.20DV - D2 Addition

An area in which patients are normally cared for, the patient vicinity is the space with surfaces likely
to be in contact with the patient or attendant who can touch the patient. This encloses a space within
the room of 1.83 m (6 ft.) beyond the perimeter of the bed (examination table, dental chair,
treatment booth, and the like) in its intended location, and extending vertically 2.29 m (7.5 ft.) above
the floor.

• Patient Environment IEC 60601-1-1
Sub clause 2.204

Such an area is an environment in which medical diagnosis, monitoring or treatment is carried out.
It is very difficult to attach unique dimensions to the PATIENT ENVIRONMENT. In practice a
distance of 2,5 m (8.2 ft.) above the floor on which the medical personnel stand and a horizontal
distance of 1,5 m (4.9 ft.) have justified themselves as indicative of the dimensions of the Patient
Environment. The patient environment/vicinity is depicted as a dashed line in this procedure - see
the example in Figure 1-1

.

Figure 1-1 Patient Safety Environment

Chapter 1 - Introduction 1-15

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

• Patient Environment EN 60601-1
Sub clause 3.79 - Patient Environment

It is difficult for this standard to define dimensions for the volume in which diagnosis, monitoring or
treatment occurs. The dimensions for the PATIENT ENVIRONMENT given in Figure 1-2 have been

justified in practice.

Figure 1-2 Example of Patient Environment

1-16 Chapter 1 - Introduction

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CAUTION

WARNINGWARNING

CAUTION

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

1-4-5 Venue Go™ Battery Safety

NOTE: The Venue Go™ ultrasound scanner is supplied with two packs of lithium ion batteries in the battery

bay.

The lithium ion batteries provide power for scanning, safely shutting down the system or placing it in
Standby mode, when an AC power source is interrupted or the AC power cable is disconnected from the
wall outlet. Lithium ion batteries last longer than conventional batteries and do not require replacement as
often. In Standby mode, you can expect 4 hours of battery life with a fully-charged battery.

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.

NOTE: Regulations vary for different countries. Dispose of a used battery in accordance with local regulations.

USE ONLY BATTERIES APPROVED BY GE AS SUITABLE FOR USE WITH THE VENUE GO™
ULTRASOUND SCANNER

The Venue Go™ battery is an approved UL device.
DO NOT ATTEMPT TO DIS-ASSEMBLE OR ALTER THE BATTERY!

Always observe the following precautions:

• 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 temperatures over 60

other heat sources.

• 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 apply solder to a battery.

• Do not connect the battery to an electrical power outlet.

TO PREVENT THE BATTERY BURSTING, IGNITING, OR FUMES FROM THE BATTERY CAUSING
EQUIPMENT DAMAGE, ALWAYS OBSERVE THE FOLLOWING PRECAUTIONS:

• Do not immerse the battery in water or allow it to get wet.

• Do not place 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, or system storage, immediately remove it and stop using it.

• If you have any questions about the battery, consult your local GE representative.

1-4-6 Patient Data Safety

o

C ( 140o F). Keep the battery away from fire and

WHILE THE SOFTWARE INSTALL PROCEDURE IS DESIGNED TO PRESERVE DATA,
YOU SHOULD SAVE ANY PATIENT DATA, IMAGES, SYSTEM SETUPS TO A A USB
FLASH DRIVE, EXTERNAL HDD, NETWORK STORAGE OR HARDCOPY BEFORE
DOING A SOFTWARE UPGRADE.

Chapter 1 - Introduction 1-17

PRELIMINARY

DANGER

WARNINGWARNING

WARNINGWARNING

DANGER

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

Section 1-5 Dangerous Procedure Warnings

Warnings, such as the examples below, precede potentially dangerous procedures throughout this
manual. Instructions contained in the warnings must be followed.

DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH, ARE PRESENT IN THIS
EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING AND
ADJUSTING.

IF THE COVERS ARE REMOVED FROM AN OPERATING VENUE GO™ SYSTEM, SOME
METAL SURFACES MAY BE WARM ENOUGH TO POSE A POTENTIAL HEAT HAZARD
IF TOUCHED, EVEN WHILE IN SHUT DOWN MODE.

EXPLOSION WARNING
DO NOT OPERATE THE EQUIPMENT IN AN EXPLOSIVE ATMOSPHERE.
OPERATION OF ANY ELECTRICAL EQUIPMENT IN SUCH AN ENVIRONMENT

CONSTITUTES A DEFINITE SAFETY HAZARD.
EQUIPMENT IS NOT SUITABLE FOR USE IN THE PRESENCE OF A FLAMMABLE ANAESTHETIC

MIXTURE WITH AIR OR WITH OXYGEN OR NITROUS OXIDE.

DO NOT SUBSTITUTE PARTS OR MODIFY EQUIPMENT

BECAUSE OF THE DANGER OF INTRODUCING ADDITIONAL HAZARDS, DO NOT INSTALL
SUBSTITUTE PARTS OR PERFORM ANY UNAUTHORIZED MODIFICATION OF THE
EQUIPMENT.

1-18 Chapter 1 - Introduction

PRELIMINARY

WARNINGWARNING

Signed

Date

TAG

&

LOCKOUT

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

Section 1-6 Lockout/Tagout (LOTO) Requirements

Follow OSHA Lockout/Tagout requirements (USA) or local Lockout/Tagout requirements by ensuring
you are in total control of the AC power plug at all times. This will protect service personnel from injuries
caused by unexpected energizing or start-up of equipment during service, repair, or maintenance.

To apply Lockout/Tagout (LOTO):

1.) Plan and prepare for shutdown.

2.) Shutdown the equipment.

3.) Isolate the equipment.

4.) Apply Lockout/Tagout Devices.

5.) Control all stored and residual energy.

6.) Verify isolation.

All potentially hazardous stored or residual energy is relieved.

ENERGY CONTROL AND POWER LOCKOUT FOR VENUE GO™ .
WHEN SERVICING PARTS OF THE SYSTEM WHERE THERE IS EXPOSURE TO
VOLTAGE GREATER THAN 30 VOLTS:

1.) FOLLOW LOCK OUT/TAG OUT PROCEDURES.

2.) TURN OFF THE BREAKER.

3.) UNPLUG THE SYSTEM.

4.) MAINTAIN CONTROL OF THE SYSTEM POWER PLUG.

5.) WAIT FOR AT LEAST 30 SECONDS FOR CAPACITORS TO DISCHARGE AS
THERE ARE NO TEST POINTS TO VERIFY ISOLATION. THE AMBER LIGHT
ON THE OP PANEL ON/OFF BUTTON WILL TURN OFF.

6.) BEWARE THAT THE MAIN POWER SUPPLY AND BACK END PROCESSOR
MAY BE ENERGIZED EVEN IF THE POWER IS TURNED OFF WHEN THE
CORD IS STILL PLUGGED INTO THE AC OUTLET.

7.) REMOVE/DISCONNECT BATTERY IF PRESENT.

Ultrasound System components may be energized.

Capacitors on Ultrasound Systems with the Shearwave Option can take up to 5
minutes to discharge.

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

Section 1-7 Product Labels and Icons

The Venue Go™ ultrasound scanner comes equipped with product labels and icons. These represent
pertinent information regarding the operation of the unit.

Figure 1-3 Venue Go™ - Labels Location

1-7-1 Universal Product Labels

NOTE: The following diagrams illustrate the labels found on the Venue Go™ ultrasound unit. For an

explanation of label icons and symbols, refer to Table 1-5 on page 1-21.

A system Rating Label (examples shown in Figure 1-4 and Figure 1-5, below) is located at the rear of
the system. This indicates the ultrasound unit’s basic power compliance. In addition, a General Label
(Figure 1-5) provides details regarding regulatory compliance - as well as warnings and cautions.

Figure 1-4 Rating Label - Venue Go™ (100-240V) International

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

Figure 1-5 General Label - International

1-7-2 Label Descriptions

The following table shows the labels and symbols that may be found on the Venue Go™ ultrasound
unit, and provides a description of each label’s purpose and location.

Table 1-5 Label Icons and Symbols - Description and Location

Label Name Description Location Source

Equipment Type BF

Type BF Applied Part, in which protection against
electric shock does not rely on basic insulation
only.
Provides additional safety precautions such as
double insulation or reinforced insulation, because
there is no provision for protective earthing or
reliance upon installation conditions.

ATTENTION- General warning sign

Attention - Consult accompanying documents:
alerts the user to refer to the user documentation
when complete information cannot be provided on
the label.

WARNING - Dangerous voltage

(the lightning flash with arrowhead in equilateral
triangle) is used to indicate electric shock hazards.

Probe
connectors and

rating plate

Various

Various.

EN/IEC 60601-1:
"Medical electrical
equipment - Part 1:
General requirements
for basic safety and
essential performance"

EN/IEC 60601-1:
"Medical electrical
equipment - Part 1:
General requirements
for basic safety and
essential performance"

EN/IEC 60601-1:
"Medical electrical
equipment - Part 1:
General requirements
for basic safety and
essential performance"

CE mark of conformity 93/42/EEC Annex XII

Indicates the Venue Go™ is a UL-approved
system (InMetro Brazil).

Pending
approval

Chapter 1 - Introduction 1-21

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

Table 1-5 Label Icons and Symbols - Description and Location (Continued)

Label Name Description Location Source

EN/IEC 60601-1:

Read the Service Manual.

Intended to alert the user to refer to the operator
manual or other instructions when complete
information cannot be provided on the label.

Various

"Medical electrical
equipment - Part 1:
General requirements
for basic safety and
essential performance"

Waste Electrical and Electronic Equipment
(WEEE) Disposal

This symbol indicates that waste electrical and
electronic equipment must not be disposed of as
unsorted municipal waste and must be collected
separately.

Prescription Requirement label

United States only

Safety Conformance Certification by Nationally
Recognized Testing Laboratory (NRTL)

Catalog number:

Indicates the manufacturer’s catalog number so
that the medical device can be identified.

Serial number

Indicates the manufacturer’s serial number so that
a specific medical device can be identified

Rating Plate

Rating Plate

• Rating Plate

• Probes

• Rating Plate

• Probes

EN 50419: Marking of
electrical and electronic
equipment in
accordance with Article
11(2) of Directive 2002/
96/EC (WEEE)

21 CFR 801.109

TUV Rheinland
Requirement

EN ISO 15223-1 Ref.

5.1.6:

Symbols for use in the
labeling of medical
devices

EN ISO 15223-1 Ref.

5.1.7:

Symbols for use in the
labeling of medical
devices

Type/Class Label Used to indicate the degree of safety or protection. Rear Panel

Date of manufacture

Manufacturer’s name and address

Authorized European Representative address

System weight

Indicates weight of the Venue Go™ ultrasound
scanner.

1-22 Chapter 1 - Introduction

• Rating Plate

• Probes

• Rating Plate

• Probes

• Rear panel

Various

EN ISO 15223-1:
Symbols for use in the
labeling of medical
devices

EN ISO 15223-1:
Symbols for use in the
labeling of medical
devices

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

Table 1-5 Label Icons and Symbols - Description and Location (Continued)

Label Name Description Location Source

EN/IEC 60601-1:

Pushing prohibited

Do not push the unit sideways when the caster
wheel brakes are in the locked position. Instability
may occur.

Rating Plate

Docking cart
rear

"Medical electrical
equipment - Part 1:
General requirements
for basic safety and
essential performance"

Loading prohibited

DO NOT place objects on the surface of the rear of
the LCD Panel while folded.

"Equipotentiality" Indicates the terminal to be used
for connecting equipotential conductors when
interconnecting (grounding) with other equipment.

Alternating current Various

Direct current

for product to be powered from a DC supply

Indicates that power is supplied to the system
(trough AC adapter or batteries)

Rating Plate

Docking cart
rear

Peripherals.

Rear panel

IEC 60878: Graphical
symbols for electrical
equipment in medical
practice

EN/IEC 60601-1:
"Medical electrical
equipment - Part 1:
General requirements
for basic safety and
essential performance"

ISO 7000 Ref. 1938

Type CF Defib-Proof Applied Part

(heart in the box with paddle) symbol is in
accordance with IEC 60878-02-06.

Protective Earth

indicates the protective earth (grounding) terminal

“Equipotentiality” indicates the 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.

Chapter 1 - Introduction 1-23

on ECG module
near ECG
patient cable
connector

Inside of AC
adapter with
system Console

Console

IEC 60417 - 5336

IEC 60417 - 5019

EN/IEC 60601-1:
"Medical electrical
equipment - Part 1:
General requirements
for basic safety and
essential performance"

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

Table 1-5 Label Icons and Symbols - Description and Location (Continued)

Label Name Description Location Source

Warning, crushing hazard: hand

This symbol indicates that this electrical and
electronic product does not contain any hazardous
substances above the maximum concentration
value established by the Chinese standard GB/T
26572, and can be recycled after being discarded,
and should not be casually discarded

This device is delivered with Electronic Instructions
for Use (eIFU). This electronic IFU can be
downloaded from the Internet. A paper copy
Instructions for Use can be ordered at no additional
cost.

This symbol indicates the product contains
hazadous materials in excess of the limits
established by the Chinese standard GB/T 26572.

Requirements of concentration limits for certain
restricted substances in electrical and electronic
products.

The number in the symbol is the Environment­friendly Use Period (EFUP), which indicates the
period during which the hazardous substances
contained in electrical and electronic products will
not leak or mutate under normal operating
conditions so that the use of such electrical and
electronic products will not result in any severe
environment pollution, any bodily injury or damage
to any assets. The unit of the period is "Year"

Rating Plate

Docking cart
rear

Bottom

Rating plate or

e-Label

China Rating
Plate

IEC 60878: Graphical
symbols for electrical
equipment in medical
practice

(EU) No 207/2012

ISO 7000 Ref. 3500

GOST - R Mark

EAC mark

GE Logo

Purpose: identify the customs country of origin of
the material (x is a country name)

Assembled in X

P/N Part Number

Note: When the Assembled in X statement is not
shown on the label, this indicates that the Customs
country of origin is the same as the country of the
legal manufacturer.

1-24 Chapter 1 - Introduction

(pending
approval)

(pending
approval)

Rear panel or

e-Label

Russian Federation No.
184-FZ

TP TC 020/2011

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

Table 1-5 Label Icons and Symbols - Description and Location (Continued)

Label Name Description Location Source

Batch code

Indicates the manufacturer’s batch code so that the
batch or lot can be identified.

Unique Device Identification (UDI) Label

Every system has a unique marking for
identification, the Unique Device Identification
(UDI) Label. The UDI label consists of a series of
alpha-numeric characters and barcode which
uniquely identify the Venue Go system as a
medical device manufactured by General Electric.
Scan or enter the UDI information into the patient
health record as required by country-specific laws.

Do not put the battery in fire. Battery pack

Do not disassemble or mistreat the battery. Battery pack

Non-Ionizing Electromagnetic Radiation Wireless
LAN

Rear panel or

e-Label

Rear panel or

e-Label

Rear panel

ISO 15223-1 Ref. 5.1.5

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

1-7-3 Venue Go™ Cart Labels Location

In addition to the labels described in the previous section, an additional label may be found on the
Venue Go™ cart, as described in the following section.

Figure 1-6 Venue Go™ System - Cart Labels Location

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

Section 1-8 Returning/Shipping Probes and Repair Parts

Equipment being returned must be clean and free of blood and other infectious substances.

GE policy states that body fluids must be properly removed from any part or equipment prior to
shipment. GE employees, as well as customers, are responsible for ensuring that parts/equipment have
been properly decontaminated prior to shipment. Under no circumstance should a part or equipment
with visible body fluids be taken or shipped from a clinic or site (for example, body coils or an ultrasound
probe).

The purpose of the regulation is to protect employees in the transportation industry, as well as the
people who will receive or open this package.

NOTE: The US Department of Transportation (DOT) has ruled that “items that were saturated and/or

dripping with human blood that are now caked with dried blood; or which were used or intended
for use in patient care” are “regulated medical waste” for transportation purposes and must be
transported as a hazardous material.

NOTE: The USER/SERVICE staff should dispose of all the waste properly, per federal, state, and local waste

disposal regulations

The Venue Go™ ultrasound scanner is not meant to be used for long-term storage of patient data or
images. The user is responsible for the data on the Venue Go™ and a regular backup is highly
recommended.

If the Venue Go™ is sent for repair, ensure that any patient information is backed up and erased from
the Venue Go™ before shipping. It is always possible during system failure and repair to lose patient
data. GE is not responsible for the loss of this data.

If PHI (Patient Healthcare Information) data needs to be sent to GE employees for service purposes,
GE will ascertain agreement from the customer. Patient information shall only be transferred by
approved service processes, tools and devices restricting access, protecting or encrypting data where
required, and providing traceability in the form of paper or electronic documents at each stage of the
procedure while maintaining compliance with cross-border restrictions of patient information transfers.

Chapter 1 - Introduction 1-27

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WARNINGWARNING

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

Section 1-9 EMC, EMI, and ESD

1-9-1 Electromagnetic Compatibility (EMC)

Electromagnetic compatibility describes a level of performance of a device within its electromagnetic
environment. This environment consists of the device itself and its surroundings, including other
equipment, power sources and persons with which the device must interface. Inadequate compatibility
results when a susceptible device fails to perform as intended due to interference from its environment,
or when the device produces unacceptable levels of emission. This interference is often referred to as
radio–frequency or electromagnetic interference (RFI/EMI) and can be radiated through space or
conducted over interconnecting power or signal cables. In addition to electromagnetic energy, EMC
also includes possible effects from electrical fields, magnetic fields, electrostatic discharge and
disturbances in the electrical power supply.

NOTE: The Venue Go™ ultrasound scanner needs special precautions regarding EMC and needs to

be installed and put into service according to the EMC information provided in the accompanying
documents (supplied with the system).

NOTE: Portable and mobile RF communications equipment can affect the Venue Go™ ultrasound scanner.

THE USE OF ACCESSORIES, TRANSDUCERS AND CABLES OTHER THAN THOSE
SPECIFIED, WITH THE EXCEPTION OF TRANSDUCERS AND CABLES SOLD BY THE
MANUFACTURER OF THE Venue Go™ AS REPLACEMENT PARTS FOR INTERNAL
COMPONENTS, MAY RESULT IN INCREASED EMISSIONS OR DECREASED IMMUNITY
OF THE Venue Go™ .

THE Venue Go™ SHOULD NOT BE USED ADJACENT TO OR STACKED WITH OTHER
EQUIPMENT AND THAT IF ADJACENT OR STACKED USE IS NECESSARY, THE Venue
Go™ SHOULD BE OBSERVED TO VERIFY NORMAL OPERATION IN THE
CONFIGURATION IN WHICH IT WILL BE USED.

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.

1-9-2 Peripherals used in the patient environment

The Venue Go has been verified for overall safety, compatibility and compliance with the following
image recording devices:

• Sony UP-D898DC

• USB 2.0/3.0 Flash Drive (Memory Stick)

• Hard Disk Drive

The Venue Go has also been verified for compatibility, and compliance for connection to a local area
network (LAN) via the rear panel Ethernet connection, provided the LAN components are IEC/EN 60950
compliant.

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

A Wireless LAN device is built into the Venue Go, and is not user-accessible (‘Connectivity’ on page 8-

29). Conforms to IEEE 802.11ac/a/b/g/n WiFi with Bluetooth 4.0 Standard. The Wireless LAN device is
an option on the system and can only be activated by installation of a special unique option key license

supplied separately by GE.

The Venue Go 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.

Accessory equipment connected to the analog and digital interfaces must be certified according to the
respective IEC standards (i.e., IEC60950 for data processing equipment and IEC60601-1 for medical
equipment). Furthermore, all complete configurations shall comply with the valid version of the system

standard IEC60601-1. Anyone connecting additional equipment to the signal input part or signal output
part of the Venue Go system is in fact configuring a medical system, and is therefore responsible to
ensure that the system complies with the requirement of the valid version of IEC60601-1. If in doubt,
consult the technical service department or your local GE representative.

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:

1.) The added device(s) must have appropriate safety standard conformance and CE Marking.

2.) There must be adequate heat dissipation and ventilation to prevent overheating of the device.

3.) The added device(s) must be used for their intended purpose having a compatible interface.

4.) Risk and leakage current of the combination must comply with IEC/EN 60601-1.

5.) Electromagnetic emissions and immunity of the combination must conform to IEC/EN 60601-1-2.

1-9-3 Compliance

The Venue Go™ ultrasound scanner conforms to all applicable conducted and radiated emission limits
and to immunity from electrostatic discharge, radiated and conducted RF fields, magnetic fields and
power line transient requirements.

NOTE: For applicable standards refer to the Safety Chapter in the Venue Go™ User Manual.

NOTE: For EMC Guidance and Manufacturer’s Declarations, refer to the tables provided in Electrostatic

Discharge (ESD) Prevention on page 1 - 30.

NOTE: For CE Compliance, it is critical that all covers, screws, shielding, gaskets, mesh and clamps are in good

condition and installed tightly without skew or stress. Proper installation following all comments noted
in this service manual is required in order to achieve full EMC performance.

Chapter 1 - Introduction 1-29

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WARNINGWARNING

WARNINGWARNING

CAUTION

WARNINGWARNING

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

1-9-4 Electrostatic Discharge (ESD) Prevention

DO NOT TOUCH ANY BOARDS WITH INTEGRATED CIRCUITS PRIOR TO TAKING THE
NECESSARY ESD PRECAUTIONS:

1.ALWAYS CONNECT YOURSELF, VIA AN ARM-WRIST STRAP CONNECTED TO THE
CAGE ASSEMBLY OR ANY GROUND SCREW WHENEVER YOU OPEN THE SYSTEM
FOR MAINTENANCE.

2.FOLLOW GENERAL GUIDELINES FOR HANDLING OF ELECTROSTATIC SENSITIVE
EQUIPMENT.

RISK OF ELECTRICAL SHOCK, SYSTEM MUST BE TURNED OFF. AVOID ALL
CONTACT WITH ELECTRICAL CONTACTS, CONDUCTORS AND COMPONENTS.
ALWAYS USE NON-CONDUCTIVE HANDLES DESIGNED FOR THE REMOVAL AND
REPLACEMENT OF ESD SENSITIVE PARTS. ALL PARTS THAT HAVE THE POTENTIAL
FOR STORING ENERGY MUST BE DISCHARGED OR ISOLATED BEFORE MAKING
CONTACT.

1-9-5 General Caution

Any changes to accessories, peripheral units or any other part of the system must be approved
by the manufacturer. Ignoring this advice may compromise the regulatory approvals obtained
for the product.

IF THE COVERS ARE REMOVED FROM AN OPERATING Venue Go™ , SOME METAL
SURFACES MAY BE WARM ENOUGH TO POSE A POTENTIAL HEAT HAZARD IF
TOUCHED, EVEN WHILE IN SHUTDOWN MODE.

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

Section 1-10 Customer Assistance

1-10-1 Contact Information

If this equipment does not operate as indicated in this Service Manual or in the Venue Go™ User
Manual, or if you require additional assistance, please contact the local distributor or appropriate

support resource, as listed below.

Prepare the following information before you call:

• Ultrasound System ID and/or serial number.

• Software version.

• Date and time of occurrence.

• Sequence of events leading to issue.

• Is the issue reproduceable?

• Imaging mode, probe, preset/application.

• Media brand, speed, capacity, type.

NOTE: Save secondary image capture, cine loop, 4D multi-volume loop.Restart the application before

resuming clinical scanning.

Table 1-6 Phone Numbers for Customer Assistance 1 of 2

LOCATION PHONE NUMBER

USA

GE

Ultrasound Service Engineering

9900 Innovation Drive

Wauwatosa, WI 53226

Canada OLC - USCAN

Latin America

EMEA

Ultrasound Europe

GE Ultraschall Deutschland GmbH

Beethovenstraße 239

Postfach 11 05 60, D-42655 Solingen

Germany

APAC

USCAN

Service: On-site

Service Parts

OLC

Application Support

LATAM

Service

Application Support

OLC - EMEA

Support Phone

Support Fax

Online Services Ultrasound Asia

ANZ Service Support

Australia

Japan

Korea

Singapore

1-800-437-1171

1-800-558-2040

1-800-321-7937 or 1-262-524-5300

1-800-682-5327 or 1-262-524-5698

1-800-321-7937

1-800-668-0732

[phone]

[phone]

[phone] - 652

[phone] - 431

1800 647 855

+(61) 1-800-659-465

+(81) 42-648-2940

+(82) 2-1544-6119

+(65) 6277-3444

China Phone

+(86) 800-810-8188

+(86) 400-812-8188

+(86) 10-6788-2652

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Table 1-6 Phone Numbers for Customer Assistance (Continued) 2 of 2

LOCATION PHONE NUMBER

India

Wipro GE Healthcare Pvt. Ltd.

4, Kadugodi Industrial Area

Bangalore - 560 067

India

Table 1-7 Phone and Fax Numbers for Manufacturer

MANUFACTURER PHONE NUMBER FAX NUMBER

GE

Ultrasound Service Engineering

9900 Innovation Drive

Wauwatosa, WI 53226

Phone

(1) 800-437-1171 (1) 414-721-3865

+(91) 1-800-425-8025

+(91) 1-800-425-7255

+(91) 1-800-102-7750

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Chapter 2

Site Preparations

Section 2-1 Overview

2-1-1 Purpose of Chapter 2

This chapter provides the information required to plan and prepare for the setup of a Venue Go™
ultrasound unit. Included are descriptions of the electrical and facility requirements that must be met by
the purchaser. A worksheet is provided at the end of this chapter (see Figure 2-3 on page 2-13) to help
ensure that all the required network information is available, prior to setup.

Chapter 2 - Site Preparations 2-1

PRELIMINARY

CAUTION

CAUTION

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

Section 2-2 Console Requirements

2-2-1 Unit Environmental Requirements

Table 2-2 Environmental Requirements

Relative Humidity

Requirement Temperature

(non-condensing) Air Pressure

Operational

Storage

Transport

+10 — +40

-20 — +60

-20 — +60

o

C (50 — 104oF)

o

C (-4 — 140oF)

o

C (-4 — 140oF))

30 — 85% 700 — 1060 hPa

10 — 70% 700 — 1060 hPa

10 — 70% 700— 1060 hPa

NOTE: The Venue Go™ system may be operated at an altitude of up to 3000 meters (9842 ft).

IF THE SYSTEM HAS BEEN IN STORAGE OR HAS BEEN TRANSPORTED, PLEASE SEE THE
ACCLIMATION REQUIREMENTS BEFORE POWERING ON AND/OR USING THE SYSTEM.
Refer to the Setup Warnings section on page 3-2.

NOTE: After a long period of storage, or after transportation of the system with the monitor in the folded-down

position (transportation mode), it is highly recommended to place the monitor in the upright position ­and to leave it in this position for a period of longer than 1 hour before use. This will enable it to properly
adjust to the environmental conditions.

2-2-2 Cooling Requirements

The cooling requirement for the Venue Go™ ultrasound unit environment is 450 BTU/hr. This figure
does not include the cooling required for lights, people, or other equipment in the room.

NOTE: Each person in the room places an additional 300 BTU/hr demand on the environmental cooling.

2-2-3 Lighting Requirements

For system setup, updates and repairs, bright lighting is required. However, operator and patient
comfort may be optimized if the room lighting is subdued and indirect when a scan is being performed.
Therefore, a combination lighting system (dim/bright) is recommended.

2-2-4 Time and Manpower Requirements.

Only one person is required to unpack the Venue Go™ ultrasound unit; at least
two people must be available to roll the system down the wheeling ramp. Attempts
to move the system considerable distances (or on an incline) by one person alone,

could result in personal injury, and/or damage to the system.

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

2-2-5 Electrical Requirements

NOTE: GE requires a dedicated mains power line and Ground for the proper operation of its Ultrasound

equipment. This dedicated power line shall originate at the last distribution panel before the
system.

Sites with a mains power system with defined Neutral and Live:

The dedicated line shall consist of one phase, a neutral (not shared with any other circuit), and a full
size Ground wire from the distribution panel to the Ultrasound outlet.

Sites with a mains power system without a defined Neutral:

The dedicated line shall consist of one phase (two lines), not shared with any other circuit, and a full
size Ground wire from the distribution panel to the Ultrasound outlet.

NOTE: Please note that image artifacts can occur, if at any time within the facility, the Ground from the

main facility's incoming power source to the Ultrasound unit is only a conduit.

2-2-5-1 Venue Go™ Power Requirements

Electrical specifications for the Venue Go™ system are as follows:

Table 2-3 Electrical Requirements

Input Voltage Tolerances Op. Current Frequency

100V AC to 240V AC ±10% 500VA 50-60 Hz

2-2-5-2 Inrush Current

Inrush current is not a factor for consideration, due to the inrush current limiting properties of the power
supplies.

Voltage

100 V 50 A

240 V 100 A

2-2-5-3 Site Power Outlets

A dedicated AC power outlet must be within reach of the unit without requiring the use of extension
cords. Other outlets adequate for the external peripherals, medical and test equipment required to
support this unit must also be present and located within 1 m (3.2 ft) of the unit. Electrical installation
must meet all current local, state, and national electrical codes.

2-2-5-4 Mains Power Plug

The Venue Go™ portable ultrasound scanner is supplied with an AC power cable, as standard. In the
event that the unit arrives without a power cable, or a power cable fitted with an incorrect plug, contact
your GE dealer. When necessary, the installation engineer will supply the appropriate power plug to
meet the applicable local regulations.

Inrush Current

(Console Only)

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

2-2-5-5 Power Stability Requirements

• Power Transients

The Venue Go™ is fully compliant with the following standard:
IEC61000-3-3 and EN\IEC60601-1-2.

2-2-6 EMI Limitations

Ultrasound machines are susceptible to Electromagnetic Interference (EMI) from radio frequencies,
magnetic fields, and transients in the air or wiring. They also generate EMI. The Venue Go™ ultrasound
unit complies with limits as stated on the EMC label. However, there is no guarantee that interference
will not occur in a particular setup.

NOTE: Possible EMI sources should be identified before the unit is installed, and should not be on the same

line as the ultrasound system. A dedicated line should be used for the ultrasound system.

Electrical and electronic equipment may produce EMI unintentionally as the result of a defect. Some of
these sources include:

• medical lasers

• scanners

• cauterizing guns

•computers

•monitors

• fans

• gel warmers

• microwave ovens

• light dimmers

• mobile phones

• in-house wireless phones (DECT phones)

• wireless computer keyboard and mouse

• air conditioning system

• High Frequency (HF) surgery equipment

• general AC/DC adapters

The presence of a broadcast station or broadcast van may also cause interference.

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

2-2-7 EMI Prevention/Abatement

The following table lists recommendations for preventing EMI:

Table 2-4 EMI Prevention/ Abatement

EMI Rule Details

Ground the unit.

Be aware of RF sources.

Replace and/or reassemble
all screws, RF gaskets,
covers and cores.

Replace broken RF gaskets.

Do not place labels where
RF gaskets touch metal.

Use GE-specified harnesses
and peripherals.

Take care with cellular
phones.

Properly address peripheral
cables.

Poor grounding is the most likely reason an ultrasound unit will have noisy images.
Check the grounding of the power cord and power outlet.

Keep the unit at least 5m (16.4 ft) away from other EMI sources. Special shielding may
be required to eliminate interference problems caused by high frequency, high powered
radio or video broadcast signals.

After you finish repairing or updating the system, replace all covers and tighten all
screws. Any cable with an external connection requires a magnet wrap at each end.
Install the shield over the front of the card cage. Loose or missing covers or RF gaskets
allow radio frequencies to interfere with the ultrasound signals.

If more than 20% or a pair of the fingers on an RF gasket are broken, replace the gasket.
Do not turn ON the unit until any loose metallic part is removed and replaced, if required.

Never place a label where RF gaskets meet the unit. Otherwise, the gap created will
permit RF leakage. In case a label has been found in such a location, move the label to
a different, appropriate location.

The interconnect cables are grounded and require ferrite beads and other shielding.
Cable length, material, and routing are all important; do not make any changes that do
not meet all specifications.

Cellular phones may transmit a 5 V/m signal that causes image artifacts.

Do not allow cables to lie across the top of the system. Loop any peripheral cable excess
length into one bundle.

2-2-8 Probe Environmental Requirements

Table 2-5 Probe Operation and Storage Temperatures

Electronics

Operation

Storage

NOTE: System and electronic probes are designed for storage temperatures of -20o to +50o C. When exposed

to large temperature variations, the probes should be kept at room temperature for a minimum of 10
hours before use.

10 — 40oC (50 — 104oF)

-20 — 50oC (-4 — 122oF)

Chapter 2 - Site Preparations 2-5

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WARNINGWARNING

CAUTION

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2-2-9 Time and Manpower Requirements

Site preparation takes time. Begin site preparation checks as soon as possible, if possible, six weeks
before delivery, to allow enough time to make any changes.

FOR CONSOLE ULTRASOUND SYSTEMS AND FOR ULTRASOUND SYSTEMS
MOUNTED ON A DOCKING/ISOLATION CART, HAVE TWO PEOPLE AVAILABLE TO
DELIVER AND UNPACK THE ULTRASOUND SYSTEM.

Attempts to move the Ultrasound system considerable distances or on an inclive
by one person, could result in injury or damage or both.

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Section 2-3 Facility Needs

2-3-1 Purchaser Responsibilities

The work and materials required to prepare the site are the responsibility of the purchaser. To avoid
delay, complete all pre-setup work before delivery. Use the Pre-setup Check List (provided in

Table 2-7 on page 2-15) to verify that all the required steps have been completed.

Purchaser responsibilities include:

• Procuring the required materials.

• Completing the preparations prior to delivery of the ultrasound system.

• Paying the costs of any alterations and modifications not specifically provided for in the sales
contract.

Note: All electrical installations that are preliminary to the positioning of the equipment at the site

prepared for the equipment must be performed by licensed electrical contractors. Other
connections between pieces of electrical equipment, calibrations, and testing must also be
performed by qualified personnel. The products involved (and the accompanying electrical
installations) are highly sophisticated and special engineering competence is required. All
electrical work on these products must comply with the requirements of applicable electrical
codes. The purchaser of GE equipment must only utilize qualified personnel to perform
electrical servicing on the equipment.

The desire to use a non–listed or customer provided product or to place an approved product further
from the Ultrasound system than the interface kit allows, presents challenges to the installation team.
To avoid delays during installation, such variances should be made known to the individuals or group

performing the installation at the earliest possible date (preferably prior to the purchase).

The ultrasound suite must be clean prior to delivery of the Ultrasound system. Carpet is not
recommended because it collects dust and creates static. Potential sources of EMI (electromagnetic
interference) should also be investigated before delivery. Dirt, static, and EMI can negatively impact
Ultrasound system reliability.

To avoid delays during setup, the individual or team who will perform the setup should be notified at the
earliest possible date (preferably prior to setup), of the existence of any of the following variances:

• Use of any non-listed product(s).

• Use of any customer provided product(s).

• Placement of an approved product further from the system than the interface kit allows.

The prepared site must be clean prior to delivery of the system. Carpeting is not recommended because
it collects dust and creates static. Potential sources of EMI should also be investigated before delivery.
Dirt, static, and EMI can negatively impact system reliability.

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2-3-2 Required Facility Needs

The following are mandatory site requirements. Additional (optional) recommendations, as well as a
recommended ultrasound room layout, are provided in section 2-3-4 - Networking Pre-Installation

Requirements (see below).

• A dedicated "hospital-grade" single branch power outlet of adequate amperage (see Table 2-3 on

page 2-3.) that meets all local and national codes and is located less than 2.5 m (8.2 ft) from the

unit’s proposed location. Refer to the Electrical Requirements section on page 2-3.

• A door opening of at least 0.54 m (1.77 ft) in width.

• Power outlets for test equipment within 1 m (3.3 ft) of the ultrasound unit.

• Material to safely clean probes (performed using a plastic container, never metal).

• In the case of a network option:

• An active network outlet in the vicinity of the ultrasound unit.

• A network cable of appropriate length (regular Pin-to-Pin network cable).

• An IT administrator who will assist in configuring the unit to work with your local network. A fixed

IP address may be required when using DICOM. Refer to the form provided in Figure 2-3 on
page 2-13 for network details that are required.

NOTE: All relevant preliminary network outlets installations at the prepared site must be performed by

authorized contractors. The purchaser of GE equipment must utilize only qualified personnel to perform
servicing of the equipment.

2-8 Chapter 2 - Site Preparations

PRELIMINARY

Scale:

Each square equals one square foot (app. 31 x 31 cm)

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2-3-2-1 Suggested Minimal Floor Plan

NOTE: GE requires a dedicated power and ground for the proper operation of its Ultrasound equipment. This

dedicated power shall originate at the last distribution panel before the Ultrasound system.

The Ultrasound system will function on voltages from 100-240 Volts and 50 or 60 Hz. However, if using
220 volt power in North America, then a center tapped power source is required.

Sites with a mains power system with defined Neutral and Live:

The dedicated line shall consist of one phase, a neutral (not shared with any other circuit), and a full
size ground wire from the distribution panel to the Ultrasound outlet.

Sites with a mains power system without a defined Neutral:

The dedicated line shall consist of one phase (two lines), not shared with any other circuit, and a full
size ground wire from the distribution panel to the Ultrasound outlet.

1.

Door – at least 762 mm (30 inches)

2. Film Viewer 9. Ultrasound system

3. Counter Top, Sink with hot and cold water and

Supplies Storage

4. Linen Supply 11. Dedicated Power Outlet -

5. Probes/Supplies 12. Network Interface

6. Examination Table – 1930 x 610 mm (76 x 24

inches)

7. Footswitch 14. GE Cabinet for Software and Manuals

8. Stool

10. External Peripherals

Circuit Breaker protected and easily accessible

13. 457 mm (18 inches) distance of Ultrasound

system from wall or objects

Figure 2-1 Minimal floor plan, 2.5 m x 3 m (8 by 10 foot)

Chapter 2 - Site Preparations 2-9

PRELIMINARY

Scale:

Each square equals one square foot (app. 31 x 31 cm)

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IRECTION 5813707-100, REVISION 2 VENUE GO™ SERVICE MANUAL

2-3-2-2 Recommended Floor Plan

1.

Secretaries or Doctors Desk

2. File Cabinet 11. Network Interface

3. Film Viewer 12. 457 mm (18 inches) distance of Ultrasound

4. Counter Top 13. Stool

5. Counter Top and Sink with hot and cold water 14. Footswitch

6. Overhead Lights Dimmer - Dual Level Lighting

(bright and dim)

7. Emergency Oxygen 16. Examination Table – 1930 x 610 mm

8. Suction Line 17. Lavatory and Dressing Room

9. Ultrasound system 18. Door – at least 762 mm (30 inches)

10. Dedicated Power Outlet - Circuit Breaker

protected and easily accessible

system from wall or objects

15. Storage for Linens and Equipment

(76 x 24 inches)

Figure 2-2 Recommended floor plan, 4.27 x 5.18 m (14 x 17 foot)

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2-3-2-3 Desirable features

• Door is at least 92 cm (3 ft.) wide

• Circuit breaker for dedicated power outlet is easily accessible

• Sink with hot and cold water

• Receptacle for bio–hazardous waste, like used probe sheaths

• Emergency oxygen supply

• Storage for linens and equipment

• Nearby waiting room, lavatory, and dressing room

• Dual level lighting (bright and dim)

• Lockable cabinet ordered by GE for its software and proprietary manuals

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2-3-3 Networking Pre-Installation Requirements

2-3-3-1 Stand-alone Unit (without Network Connection)

None.

2-3-3-2 Unit Connected to Hospital’s Network

Supported networks:

• Wireless LAN (Wi-Fi)

• 10/100/1000 Mbps Ethernet

2-3-3-3 Purpose of the DICOM Network Function

DICOM services provide the operator with clinically useful features for moving images and patient
information over a hospital network. Examples of DICOM services include the transfer of images to
DICOM servers for storage and to workstations for viewing images. As an added benefit, transferring
images in this manner enables viewing to be done on reviewing station, while scanning continues.

2-3-3-4 DICOM Option Pre-Installation Requirements

To configure the Venue Go™ ultrasound unit to work with other network connections, the network
administrator must provide the required information, which should include the following:

• Details: DICOM network details for the Venue Go™ unit, including the

host name, local port, IP address, AE title and network subnet
mask.

• Routing Information: IP addresses for the default gateway and other routers in use at

the site.

• DICOM Application Information:Details of the DICOM devices in use at the site, including the

DICOM host name, AE title and IP addresses.

2-12 Chapter 2 - Site Preparations

PRELIMINARY

Site System Information

Services (Destination Devices)

TCP/IP Settings

Device Type

Manufacturer

Name

IP Address

Port

AE Title

1
2
3
4
5
6
7
8

9
10
11
12

Dept:

Venue Go™
SN:

Type:

Floor:

Room:

REV:

Comments:

CONTACT INFORMATION

Name

Title

Phone

E-Mail Address

Site:

Scanner IP Settings

IP Address:

Subnet Mask:

Default Gateway:

Name - AE Title:

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Section 2-4 Connectivity Installation Worksheet

Figure 2-3 Connectivity Installation Worksheet

Chapter 2 - Site Preparations 2-13

PRELIMINARY

Venue Go™

Host Name

AE Title

Local Port

IP Address

Net Mask

...

...

ROUTING INFORMATION

ROUTER2
ROUTER3

ROUTER1

...

...

...

...

...

...

...

Destination
IP Addresses

GATEWAY IP Addresses

Default

DICOM APPLICATION INFORMATION

NAME

Store 2

Store 3

Store 1

MAKE/REVISION IP ADDRESSES PORTAE TITLE

Store 5

Store 6

Store 4

Storage
Commit

MPPS

Work list

...

...

...

...

...

...

...

...

...

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Figure 2-4 Worksheet for DICOM Network Information

2-14 Chapter 2 - Site Preparations

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Table 2-6 Venue Go™ Pre-Setup Check List

Action Yes No

Schedule at least 2 hours for setup of the system.

Notify setup team of the existence of any variances from the basic setup.

Make sure system and probes have been subject to acclimation period.

Environmental cooling is sufficient.

Lighting is adjustable to adapt to varying operational conditions of the scanner.

Electrical facilities meet system requirements.

EMI precautions have been taken and all possible sources of interference have been
removed.

Mandatory site requirements have been met.

If a network is used, IP address has been set for the system and a dedicated network
outlet is available.

This page was intentionally left blank.

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Chapter 3

System Setup

Section 3-1 Overview

3-1-1 Purpose of Chapter 3

This chapter provides instructions for setting up the Venue Go™ ultrasound unit. Before beginning the
setup process, an appropriate site must be prepared, as described in Chapter 2 - Site Preparations.
Once the site has been prepared, setup can proceed as described in this chapter.

Included in this chapter are guidelines for transporting the unit to a new site, as well as procedures that
describe how to receive and unpack the equipment, and (if necessary) how to file a damage or loss
claim. Instructions for checking and testing the unit, probes, and external peripherals for electrical safety
are also provided.

NOTE: A Venue Go™ is ready for use only if the tests and checks described in Chapter 3 -System

Setup (this chapter) and Chapter 4 -General Procedures and Functional Checks of this Service

Manual meet the expected results.

Chapter 3 - System Setup 3-1

PRELIMINARY

CAUTION

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Section 3-2 Setup Reminders

3-2-1 Average Setup Time

The Venue Go™ setup and functional checkout will take approximately one hour; Venue Go™
consoles with optional equipment may take slightly longer.

Once the site has been prepared, the average installation time required is shown in Ta bl e 3- 9 below.

Table 3-8 Average Setup Time

Average

Description

Setup Time

Comments

Unpacking the scanner

Setting up the scanner

DICOM Option
(connectivity)

Setting up InSite

15 minutes

30 minutes Time may vary, according to the required configuration

30 minutes Time may vary, according to the required configuration

30 minutes

3-2-2 Setup Warnings

1.) The Venue Go™ ultrasound scanner weighs approximately 6 Kgs (13.22 lbs), without add-ons/
peripherals. System cart weighs approximately 27 kg (59.5 lbs).
Two people are always required to unpack the system cart.

2.) There are no operator-serviceable components. To prevent shock, do not remove any covers or

panels. If problems or malfunctions occur, unplug the power cord. Only qualified service personnel
should carry out servicing and troubleshooting.

NOTE: For information on shipping carton labels, refer to Figure 3-3 on page 3-5 and Figure 3-4 on

page 3-6.

3-2-2-1 System Acclimation Time

Following transport, the Venue Go™ system may be very cold, or hot. Allow time for the system to

acclimate before being switched ON. Acclimation requires 1 hour for each 2.5

temperature of the system is below 10

o

C or above 40oC.

o

C increment, when the

Turning the system ON after arrival at the site - without allowing time for acclimation - may
cause system damage!

6

Table 3-9 Venue Go™ System Acclimation Time

-40 -35 -30 -25 -20 -15 -10 -5 0 5 10 35 40 45 50 55 60

°C

-40 -31 -22 -13 -4 5 14 23 32 41 50 95 104 113 122 131 140

°F

20 18 16 14 12 10 8 4 2 0 0 0 2 4 6 8

Hrs

3-2 Chapter 3 - System Setup

PRELIMINARY

DANGER

WARNINGWARNING

CAUTION

CAUTION

CAUTION

CAUTION

WARNINGWARNING

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3-2-3 Safety Reminders

WHEN USING ANY TEST INSTRUMENT THAT IS CAPABLE OF OPENING THE
AC GROUND LINE (I.E., METER’S GROUND SWITCH IS OPEN), DO NOT TOUCH
THE UNIT!

TWO PEOPLE ARE REQUIRED TO UNPACK THE SYSTEM CART AS IT IS HEAVY.
TWO PEOPLE ARE ALWAYS REQUIRED WHENEVER A PART WEIGHING 16KG (35 LB.)
OR MORE MUST BE LIFTED.

IF THE UNIT IS VERY COLD OR HOT, DO NOT TURN ON POWER TO THE UNIT UNTIL IT HAS
HAD SUFFICIENT TIME TO ACCLIMATE TO ITS OPERATING ENVIRONMENT.

TO PREVENT ELECTRICAL SHOCK, CONNECT THE UNIT TO A PROPERLY GROUNDED
POWER OUTLET.

DO NOT USE A THREE-PRONG TO TWO-PRONG ADAPTER, AS THIS DEFEATS SAFETY
GROUNDING.

DO NOT WEAR THE ESD WRIST STRAP WHEN YOU WORK ON LIVE CIRCUITS WHERE MORE
THAN 30 V PEAK IS PRESENT.

DO NOT OPERATE THE UNIT UNLESS ALL BOARD COVERS AND FRAME PANELS ARE
SECURELY IN PLACE, TO ENSURE OPTIMAL SYSTEM PERFORMANCE AND COOLING.
(WHEN COVERS ARE REMOVED, EMI MAY BE PRESENT).

ACOUSTIC OUTPUT HAZARD
ALTHOUGH THE ULTRASOUND ENERGY TRANSMITTED FROM THE Venue Go™
PORTABLE ULTRASOUND SCANNER IS WITHIN AIUM/NEMA STANDARDS AND FDA
LIMITATIONS, AVOID UNNECESSARY EXPOSURE. ULTRASOUND ENERGY CAN
PRODUCE HEAT AND MECHANICAL DAMAGE

NOTE: The Venue Go™ User Manual should be fully read and understood before operating the unit.

Keep the manual near the unit for reference.

.

Chapter 3 - System Setup 3-3

PRELIMINARY

CAUTION

CAUTION

CAUTION

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Section 3-3 Receiving and Unpacking the Equipment

3-3-1 Warnings for Receiving and Unpacking the Equipment

Two people are needed to unpack the Venue Go cart because of its weight.

Two people are required whenever a part weighing 16 KG (35 LBS) or more must be lifted

Remember to use relevant personal protecting equipment (PPE) during packing and unpacking.
Check with your local EHS representative.

3-3-2 Overview

Please read this section fully before unpacking the Venue Go™ ultrasound unit.

The Venue Go™ ultrasound unit, together with the peripherals, cables, and accessories, are shipped
from the factory in a single shipping cardboard box.

Figure 3-1 Venue Go™ Package

Table 3-10 Venue Go™ System Shipping Carton - Dimensions and Weights

Description Height Width Depth

Venue Go™ scanner

with peripherals and accessories

44 cm

17.3 ins

a.

3-4 Chapter 3 - System Setup

56 cm
22 ins

26 cm

10.2 ins

Weight

10.5 Kg

23.149 lbs

a

PRELIMINARY

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Table 3-11 Venue Go™ Box Contents

# Description

1 Venue Go™ system

2 AC-DC Adapter 24V

3 Multipurpose cup gel bottle insert

4 Small probe insert

5 Power cord

6 Venue Go™ SW media

3-3-3 Unpacking Venue Go™ System

1.) Open the system package and remove the top foam.

Figure 3-2 Open the system Box

2.) Take out the system from the zipper bag and remove the upper cover foam.

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3.) Remove the back system foam.

Figure 3-3 Remove system from zipper bag

4.) Remove the middle foam.

5.) Take out all accessories.

Figure 3-4 Remove accessories

3-6 Chapter 3 - System Setup

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CAUTION

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3-3-4 Unpacking Venue Go™ Cart

Two people are needed to unpack the Venue Go cart because of its weight.

Two people are required whenever a part weighing 16 KG (35 LBS) or more must be lifted

1.) Open the box and identify the base protective foam.

Figure 3-5 Open the Cart Box

2.) Remove the base protective foams, and expose the wheels.

Figure 3-6 Remove Base Protective Foam

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3.) Position the cart on its wheels.

Figure 3-7 Position the Cart on its Wheels

4.) Unlock the cart wheels.

5.) Use the tray handle to roll out the cart from the box.

Figure 3-8 Roll out the Cart using the Tray Handle

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6.) Remove the rest of the foam covers. .

Figure 3-9 Remove the rest of the foam covers

7.) Take the rest of the parts out of the box, remove the protective foam covers.

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3-3-5 Physical Inspection

3-3-5-1 System Voltage Settings

CONNECTING A VENUE GO™ SCANNER TO INCORRECT VOLTAGE LEVEL WILL
MOST LIKELY DESTROY IT.
CONNECT THE SYSTEM ONLY IN ACCORDANCE WITH THE VOLTAGE INDICATED ON
THE PRODUCT LABEL.

3-3-6 EMI Protection

The Venue Go™ Ultrasound Unit has been designed to minimize the effects of Electro Magnetic
Interference (EMI). Many of the covers, shields, and screws are provided primarily to protect the system
from image artifacts caused by this interference. For this reason, it is imperative that all covers and
hardware are installed and secured before the unit is put into operation.

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Section 3-4 Preparing for Setup

3-4-1 Verifying Customer Order

Compare items received by the customer to that which is listed on the delivery order. Report any items
that are missing, back ordered, or damaged.

3-4-2 Physical Inspection

Verify that the Venue Go™ arrived intact (visual inspection).

If the Venue Go™ has been damaged, please refer to DAMAGE IN TRANSPORTATION on page x in
the beginning of this manual.

3-4-3 Component Inspection

After verifying that all the required parts are included in the shipping crate, inspect the system components
using the checklist supplied below. In addition, ensure that all the labels described in Chapter 1 -

Introduction are present, accurate and in good condition, and enter the serial number printed on the main

label into the system installation details card, as described in Paperwork After Setup on page 3-64.

3-4-3-1 Damage Inspection Checklist

Visually inspect the contents of the shipping carton for damage. If any parts are damaged or missing,
contact an authorized GE Service Representative.

A Damage Inspection Checklist for t he Venue Go™ p ortable ultraso und s canner i s provid ed in Tab le 3 -

13 below.

Table 3-12 Damage Inspection Checklist - Venue Go™ Systems

Step Item Recommended Procedure

Venue Go™

1

System

2

Probes

3

Rear Panel

4

Power Cord/s

5

Venue Go™ Cart Check that there are no dents or scratches and that no internal parts are exposed.

6

Peripherals

Verify that the system is switched OFF and unplugged. Clean the system. Check
that there are no dents or scratches and that no internal parts are exposed.

Check all probes for wear and tear on the lens, cable, and connector. Look for bent
or damaged pins on the connector and in the connector socket on the unit. Verify
that the EMI fingers around the probe connector socket housing are intact. Check
the probe locking mechanism and probe switch.

Check the rear panel connectors for bent pins, loose connections and loose or
missing hardware. Screw all the cable connectors tightly to the connector sockets
on the panel. Verify that the labeling is in good condition.

Check the power cord for cuts, loose hardware, tire marks, exposed insulation, or
any deterioration. Verify continuity.

Check and clean the peripherals in accordance with the manufacturer’s directions.
To prevent EMI or system overheating.

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2

3

4

5

6

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3-4-3-2 General View of the Venue Go™ Ultrasound Unit

.

Figure 3-1 General View of the Venue Go™ Ultrasound Scanner

# Item

1 Front Panel Display:
2 Kick stand
3 Probe holder
4 Probe connectors
5 I/O panel
6 Fan outlet
7 Battery cover

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3-4-3-3 Venue Go™ Cart Overview

Figure 3-2 Venue Go™ Rear View

# Item # Item

1 Venue Go™ System 8 Accessories basket

2 Cart Cradle 9 AC cable connector to cart

3 Vertical/horizontal tilt adjustment 10 Cradle system latch

4 Up/down adjustment column. 11 Printer bay with mounted printer

5 Multipurpose front and rear handles 12 ECG module

6 Height adjustment handle 13 Cart Labels

7 AC adapter box cover

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3-4-3-4 Peripheral/Accessory Interface Panel

Figure 3-18 shows a view of the Venue Go™ ultrasound unit rear panel showing external peripheral/

accessory connectors.

Figure 3-3 View of the Venue™ Peripheral/Accessory Interface Panel

1 Ethernet LAN connector — 1000 Base-TX Ethernet IEEE 802.3 (3kV insulation)
2 USB 3.0 connector x3 (not insulated)
3 HDMI connector (not insulated)

3-4-3-5 EMI Protection

The Venue Go™ has been designed to minimize the effects of Electro-Magnetic Interference (EMI).
Many of the covers, shields, and screws are provided primarily to protect the Venue Go™ from image
artifacts caused by this interference. For this reason, it is imperative that all covers and hardware are
installed and secured before the Venue Go™ is put into operation.

See EMI Limitations on page 2 - 4 for more information about EMI protection.

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Section 3-5 Completing the Setup

3-5-1 Purpose of this Section

This section describes how to complete the setup of the Venue™.

3-5-2 System Specifications

3-5-2-1 System Requirements Verification

• Verify that the site meets the requirements listed in Chapter 2.

(See: Facility Needs on page 2 - 7.)

• Verify that the specifications below do not conflict with any on-site conditions.

3-5-2-2 Physical Dimensions

Table 3-13 Physical Dimensions of Venue Go™ System Only

Height Width Depth Unit

33 41 12 cm

13 16.14 4.72 Inches

Table 3-14 Physical Dimensions of Venue Go™ Mounted on Cart

Max. Height Max. Width Max. Depth Unit

125.5 51.5 49 cm

49.4 20.27 19.29 Inches

3-5-2-3 Mass with Monitor and Peripherals

Table 3-15 Mass of Venue Go™ without Cart and Peripherals

Model Mass [KG] Mass [LBS]

Venue Go™ 6 13.22

3-5-2-4 Acoustic Noise Level

Less than 55 dB(A) at 20 degrees Celsius, measured in the operators head position, 20 cm in front of
the keyboard’s right corner, at 1.30 m above the floor, and in a distance of 1 meter at all four sides, 1
meter above the floor.

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3-5-3 Electrical Specifications

Connecting a Venue Go™ to the wrong voltage level will most
likely destroy it.

3-5-3-1 Verification of the Venue Go™ Voltage Setting

Verify that the mains voltage specified for the Venue Go™ is available on-site.

The voltage setting for the Venue Go™ is found on a label near the Mains Power Circuit Breaker on
the rear of the Venue Go™ .

3-5-3-2 Electrical Specifications for the Venue Go™

In the table below, the electrical specifications for Venue Go™ includes monitor and on board
peripherals.

Table 3-16 Electrical Specifications for all Venue Go™ Models

Voltage 100-240 VAC ±10%

Power Consumption
(system only)

Power Consumption

(with cart and peripherals)

Frequency 50-60 Hz

The system only current drain will vary depending on the mains voltage.

• At 240 VAC the current may be up to 1.04 A.

• At 100 VAC the current may be up to 2.5 A.

250 Watt

350 Watt

3-5-4 Connections on the I/O Rear Panel

NOTE: Accessory equipment connected to the analog and digital interfaces must be certified according to the

respective IEC standards (e.g. IEC60950 for data processing equipment and IEC60601-1 for medical
equipment). Furthermore, all complete configurations shall comply with the valid version of the system
standard IEC60601-1-1. Everybody who connects additional equipment to the signal input part or signal
output part of Venue Go™ , configures a medical system, and is therefore responsible that the
Ultrasound system complies with the requirements of the valid version of IEC60601-1-1. If in doubt,
consult the technical service department or your local representative for GE.

3-5-4-1 Network Connection

Connect the network cable to the Ethernet connector on the External I/O.

The connector is located on the rear side of Venue Go™ .

3-5-5 Connecting Probes

3-5-5-1 Introduction to Connecting Probes

Probes can be connected or changed any time, as described below, regardless of whether the system
is powered ON or OFF.

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The Venue Go™ has three RS connectors.

Figure 3-4 Probe Connectors on Venue Go™

HANDLE THE PROBE GENTLY WHILE CONNECTING AND DISCONNECTING.
DO NOT TOUCH THE PATIENT AND ANY OF THE CONNECTORS ON THE ULTRASOUND UNIT

SIMULTANEOUSLY, INCLUDING ULTRASOUND PROBE CONNECTORS.

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3-5-5-2 Connect a Probe

NOTE: It is not necessary to turn OFF power to connect or disconnect a probe.

Do not allow the probe head to hang freely. Excessive impact
to the probe will result in irreparable damage.

To prevent probe connector pins damage, or PCB board
damage, do not use excessive force when connecting the
probes.

Keep the probe cables away from the wheels.

Do not bend the probe cables.

Do not cross cables between probes.

There are 3 probe connectors on the rear side of the system. Each connector is comprised of a probe­socket and a locking latch.

Figure 3-5 Venue Go™ Probe Connectors

1) Before connecting the probe:

a.) Do a visual check of the probe pins and system sockets.

b.) Remove any dust or foam rests from the probe pins.

c.) Verify the probe and the probe cable for any visual damage.

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To connect a probe to one of the sockets 1, 2, or 3:

1) Hold the probe connector vertically with the cable pointing upward.

2.) Prior to inserting the probe, ensure that the connector locking handle is positioned to the left.

3) Align the connector with the probe port and carefully push into place.

4) Push the connector locking handle to the right to secure the probe connector.

5) Carefully position the probe cord so it is free to move and is not resting on the floor.

3-5-5-3 Disconnect Probes

Follow these steps to disconnect the RS probes, as applicable:

1) Move the connector locking lever to the left to unlock the connector.

2) Carefully remove the connector from the port.

3) Ensure that the probe head is clean before placing the probe in its storage case.

For cleaning instructions, see the User Manual.

3-5-6 Power on/Boot up

For procedure, see: Power ON/Boot-up on page 4 - 3.

3-5-7 Power Shut Down

For procedure, see: Power Shutdown on page 4 - 5.

3-5-8 Complete Power Down

For procedure, see: Complete Power Down on page 3 - 19.

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Section 3-6 Configuration

3-6-1 Purpose of this Section

This section describes how to configure the Venue Go™ .

3-6-2 Venue Go™ Configuration

3-6-2-1 EZ Configuration Wizard

The Venue Go™ Configuration Wizard enables the user to easily configure the system, after SW
installation.

1.) After the system reboots, the Venue Go™ setup wizard welcome screen appears:

2.) Select the interface language and tap OK to proceed.

Figure 3-6 Venue Go™ Installation Wizard - Welcome Screen

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3.) Tap Run wizard to continue the installation.

Figure 3-7 Venue Go™ Installation Wizard - Run Wizard

The settings screen appears. The Local tab opens by default.

4.) On the Local tab, enter the required details and tap Save. Then, proceed to the next tab.

Figure 3-8 Venue Go™ Installation Wizard - Local Tab

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5.) On the Network tab, define the required settings and tap Save.Then, proceed to the next tab.

Figure 3-9 Venue Go™ Installation Wizard - Network Tab

6.) On the Thermal Printer tab, configure the printer and tap Save. Then, proceed to the next tab. If

the printer is already configured, skip this step and proceed to the next one.

Figure 3-10 Venue Go™ Installation Wizard - Thermal Printer Tab

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7.) On the InSite tab, define the required settings and tap Submit Changes. Make sure you fill all

mandatory fields (highlighted in bold). Then, proceed to the next tab.

Figure 3-11 Venue Go™ Installation Wizard - InSite Tab

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8.) On the Connectivity tab, enable the required settings in the Connectivity items list, by moving the

On/Off sliders to On. Then, select each Connectivity item to define its properties. Tap Apply and
then Save.Then, proceed to the next tab.

Figure 3-12 Venue Go™ Installation Wizard - Connectivity Tab

9.) On the OptionKey tab, enter the key string to enable the purchased options and tap Save. Then,

proceed to the next tab.

Figure 3-13 Venue Go™ Installation Wizard - OptionKey Tab

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10.)On the Reports tab, view the defined settings and tap Save As to save the report. Save the report

on USB flash memory.Then, proceed to the next tab.

Figure 3-14 Venue Go™ Installation Wizard - Report Tab

11.)On the About tab, view all settings defined on each tab, and click Save to save the entire set of

defined settings. Then click Exit, to exit the Setup Wizard.

Figure 3-15 Venue Go™ Installation Wizard - About Tab

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3-6-2-2 Select System Settings Screen

1) On the Home screen tap: Settings >> Config.

Figure 3-16 Home Screen - Settings Menu

2) Log on as adm.

Figure 3-17 Operator Login

3) From the Config side menu, select System >>Settings
The System Settings screen is displayed.

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