Logiq v2

GE
Technical Publication
LOGIQ V2/LOGIQ V1
Basic Service Manual
Direction Number: 5610739-100 English
Rev.10
All Material Copyright © 2015-2017 by General Electric Company Inc.

All Rights Reserved.
Product Information
This Manual covers the software version of R1.x.x for LOGIQ V2, LOGIQ V1
ultrasound system.
GE
Copyright © 2015-2017, General Electric Company.

GE Medical Systems, a General Electric Company, going to
market as GE
Manufacturer:
GE Medical Systems (China) Co., Ltd.
No. 19, Changjiang Road
WuXi National Hi-Tech Development Zone
Jiangsu, P.R. China 214028
TEL: +86 510 85225888; FAX: +86 510 85226688
www.gehealthcare.com
Revision history
Revision History
Date
Revision (YYYY/MM/DD) Reason for change
Rev.1 2015/06/09 Initial Release
Rev.2 2015/11/13 New software version, general update
Rev.3 2015/11/23 Add software wipe information
Rev.4 2016/01/05 Update spare part list
Rev.7 2016/11/21 Change safety test frequency
Rev.8 2017/02/23 Update software loading procedure
Rev.10 2017/10/31 Add ECG Installation
List of Effected Pages (LOEP)
Chapter Revision Chapter Revision
Front Rev.10 Chapter 6 Rev.10
Front matter Rev.10 Chapter 7 Rev.10
TOC Rev.10 Chapter 8 Rev.10
Chapter 1 Rev.10 Chapter 9 Rev.10
Chapter 2 Rev.10 Chapter 10 Rev.10
Chapter 3 Rev.10 Index Rev.10
Chapter 4 Rev.10 Rear Cover Rev.10
Chapter 5 Rev.10
Please verify that you are using the latest revision of this document. Information
pertaining to this document is maintained on MyWorkshop/ePDM (GE electronic Product
Data Management). If you need to know the latest revision, contact your distributor, local
GE Sales Representative or in the USA call the GE Ultrasound Clinical Answer Center at
1 800 682 5327 or 1 262 524 5698.
LOGIQ V2/LOGIQ V1 – Basic Service Manual i-1

5610739-100 English Rev.10
Important precautions
Translation policy
i-2 LOGIQ V2/LOGIQ V1 – Basic Service Manual

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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.

5610739-100 English Rev.10
Omission and errors
If there are any omissions, errors or suggestions for improving
this documentation, contact the GE Global Documentation
Group with specific information listing the system type, manual
title, part number, revision number, page number and
suggestion details.
Mail the GE Medical Systems (China) Co., Ltd.
information to: No. 19 Changiang Road
Wuxi National Hi-Tech Dev. Zone
Jiangsu
P.R.China 214028
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.

5610739-100 English Rev.10
Service Safety Considerations
DANGER DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH,

ARE PRESENT IN THIS EQUIPMENT. USE EXTREME
CAUTION WHEN HANDLING, TESTING AND ADJUSTING.
WARNING 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, refer to

Chapter 1 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 may revise this publication from time to time without written
notice.
Trademarks
All products and their name brands are trademarks of their
respective holders.
Copyrights
All Material Copyright © 2015-2017 by
General Electric Company Inc. All Rights Reserved.

5610739-100 English Rev.10
5610739-100 English Rev.10
Table of Contents
Translation policy - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-2

Damage in transportation - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-14
Certified electrical contractor statement - For USA Only - - - - - - - - - - - - i-14
Omission and errors - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-15
Service Safety Considerations - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-16
Legal notes - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-17
Trademarks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-17
Copyrights - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-17
Table of Contents
Chapter 1 — Introduction
Overview
Contents in this chapter- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-2
Manual Overview
Contents in this manual - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-3
Typical users of the Proprietary Service Manual - - - - - - - - - - - - - - - - - 1-4
LOGIQ V2/LOGIQ V1 models covered by this manual - - - - - - - - - - - - - 1-5
Important conventions
Conventions used in book - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-6
Standard hazard icons - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-8
Product icons
Labels locations
Safety considerations
Contents in this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-13
Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-13
Human Safety - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-13
Mechanical safety - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-16
Electrical safety - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-18
Battery Safety- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-20
Dangerous procedure warnings
Lockout/Tagout (LOTO) requirements
Returning probes and repair parts
EMC, EMI and ESD
What is EMC? - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-25
CE Compliance - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-25
Electrostatic discharge (ESD) prevention - - - - - - - - - - - - - - - - - - - - - 1-26
Customer assistance
Contact information- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-27
Phone numbers for Customer Assistance - - - - - - - - - - - - - - - - - - - - - 1-28
System manufacturer - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-28

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Authorized Representative- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-29
Chapter 2 — Site Preparations
Overview
General Ultrasound system requirements
Contents in this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-3
Ultrasound system environmental requirements- - - - - - - - - - - - - - - - - - 2-3
Electrical requirements - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-6
EMI limitations - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-9
Probes environmental requirements - - - - - - - - - - - - - - - - - - - - - - - - - 2-11
Time and manpower requirements - - - - - - - - - - - - - - - - - - - - - - - - - - 2-11
Facility needs
Contents in this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-12
Purchaser responsibilities - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-13
Required facility needs - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-14
Desirable features- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-15
Minimal floor plan suggestion- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-16
Recommended floor plan suggestion - - - - - - - - - - - - - - - - - - - - - - - - 2-17
Suggested floor plan, Ultrasound system, and EchoPAC PC in same
room - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-18
Networking setup requirements - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-19
Environmental Dangers
Patient Environment IEC60601-1 and ANSI AAMI ES60601-1 - - - - - - 2-22
Chapter 3 — System Setup
Overview
Setup reminders
Average setup time - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-3
Setup warnings- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-3
Receiving and unpacking the equipment
Purpose of this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-6
Contents in this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-6
Warnings for receiving and unpacking - - - - - - - - - - - - - - - - - - - - - - - - 3-6
Receiving the LOGIQ V2/LOGIQ V1 - - - - - - - - - - - - - - - - - - - - - - - - - - 3-6
Unpacking the LOGIQ V2/LOGIQ V1 - - - - - - - - - - - - - - - - - - - - - - - - - 3-8
Packing the Equipment - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-11
Packing materials - recycling information
Preparing for setup
Verify customer order - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-13
Physical inspection - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-13
EMI protection - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-13
Completing the setup
Purpose of this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-14
Contents in this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-14
System specifications - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-14
Electrical specifications - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-15
Peripheral/Accessories Connector Panel - - - - - - - - - - - - - - - - - - - - - 3-16

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Connecting probes - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-17
Powering the system- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-17
System Configuration
LOGIQ V2/LOGIQ V1 configuration - - - - - - - - - - - - - - - - - - - - - - - - - 3-18
Peripherals Installation
Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-19
Furnished materials - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-20
Peripherals Installation Instructions - - - - - - - - - - - - - - - - - - - - - - - - - 3-22
Connectivity setup
TCP/IP Screen - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-34
Network setup - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-35
Setup the LOGIQ V2/LOGIQ V1 for DICOM Communications - - - - - - - 3-36
How to get the LOGIQ V2/LOGIQ V1 to recognize another Device on the
Network - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-38
How to Setup and Use a DICOM Image Storage Service - - - - - - - - - - 3-39
Option Setup
Software Option Installation Procedure - - - - - - - - - - - - - - - - - - - - - - - 3-40
Paperwork after setup
Contents in this Section- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-42
User’s Manual(s) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-42
Product Locator Installation Card - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-42
Chapter 4 — General Procedures and Functional Checks
Overview
Purpose of this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-2
Special Equipment required - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-2
General procedures
Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-4
Power ON/Boot Up - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-5
Power off - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-9
Logging on to LOGIQ V2/LOGIQ V1 as “ADM” - - - - - - - - - - - - - - - - - 4-11
Service Key (Dongle, HASP) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-12
Exit to Windows Desktop from the LOGIQ V2/LOGIQ V1 application
software - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-13
Removable media - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-17
Archiving and loading presets - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-18
Data Management - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-20
Backup - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-20
Restore the factory defaults - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-20
Installation and Setup Procedure for Peripherals - - - - - - - - - - - - - - - - 4-20
Where are the User Manuals and the Service Manual? - - - - - - - - - - - 4-21
How to display or print the PDF files from the Manual CD? - - - - - - - - - 4-21
Cleaning the Trackball- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-22
Functional checks
Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-24
Contents in this Section- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-24

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Preparation - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-24
Basic Controls - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-25
Operator Panel - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-25
Performance Tests - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-26
B mode Checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-27
M Mode Checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-28
Color Mode Checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-29
Adjust the Color Mode controls - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-30
Select Color M Mode- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-31
PW Doppler Mode Checks- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-33
Adjust the PW Doppler Mode controls- - - - - - - - - - - - - - - - - - - - - - - - 4-34
Tissue Velocity Imaging (TVI) Checks- - - - - - - - - - - - - - - - - - - - - - - - 4-35
Adjust the TVI Controls - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-36
Basic Measurements- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-36
Probe/Connectors Check- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-37
Cineloop Check - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-38
Preparation - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-38
Adjust the Cineloop controls - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-38
Back End Processor checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-39
Operator Panel Test - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-39
Peripheral checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-39
Turn OFF Power to LOGIQ V2/LOGIQ V1- - - - - - - - - - - - - - - - - - - - - 4-39
Power supply test & adjustments
Power Supply Test Procedure - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-40
Power Supply Adjustment - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-40
Application Turnover Check List
Software Configuration Checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-41
Site Log
Chapter 5 — Components and Functions (Theory)
Overview
Block Diagram and Theory
General Information - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-3
Top Console- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-3
Block Diagram - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-4
Power Diagram
Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-5
AC Power - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-5
Common Service Platform
Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-6
Chapter 6 — Service Adjustments
Overview
LCD Monitor adjustments
Purpose of this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-3
Monitor Adjustments - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-3

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Software Reload
Confirm Backups for Patient Data and Presets - - - - - - - - - - - - - - - - - - 6-4
System Reload procedure - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-5
Chapter 7 — Replacement Procedures
Overview
Warnings and important information
Warnings - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-3
Returning/shipping probes and repair parts - - - - - - - - - - - - - - - - - - - - - 7-4
Disassembly/Re-assembly
Warning and Caution - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-5
Tools needed for servicing LOGIQ V2/LOGIQ V1 - - - - - - - - - - - - - - - - 7-6
Trackball Roller Cleaning- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-7
2-Probe Holder (5727508) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-8
Paper Tray Kit (5727505) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-10
Printer Shelf (5727506) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-11
Loading the software
Customer provided prerequisite - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-13
Data Management - moving all images - - - - - - - - - - - - - - - - - - - - - - - 7-13
Backing up the Patient Archive and System Configurations - - - - - - - - 7-14
Recording important settings and parameters - - - - - - - - - - - - - - - - - - 7-14
Loading the System Software - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-15
Chapter 8 — Diagnostics/Troubleshooting
Overview
Gathering Trouble Data
Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-3
Collect Vital System Information- - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-3
Collect a Trouble Image with Logs - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-4
Screen Capture
Button screen - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-5
Setting the Store Key to Screen Capture- - - - - - - - - - - - - - - - - - - - - - - 8-6
Capturing a Screen - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-7
Reset the Store Key to Customer’s Functionality - - - - - - - - - - - - - - - - - 8-9
Common Diagnostics
Utilities- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-10
Service Diagnostics - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-15
OP Panel Interface - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-25
Restart the system after diagnostics - - - - - - - - - - - - - - - - - - - - - - - - - 8-25
Network Configuration
Wire-LAN Network - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-26
Chapter 9 — Renewal Parts
Overview
Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-2

5610739-100 English Rev.10
List of Abbreviations
Renewal Parts Lists
AC Power Cord - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-4
Operator Console Assy - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-5
V Cart - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-5
V Cart - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-6
Probe and Accessories - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-9
Peripheral - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-10
Power Cord - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-12
V Cart With Package- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-12
Manuals- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-13
Chapter 10 — Care and Maintenance
Overview
Contents in this chapter- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-2
Warnings
Why do maintenance
Periodic maintenance inspections - - - - - - - - - - - - - - - - - - - - - - - - - - 10-4
Keeping records - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-4
Quality assurance - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-5
Maintenance task schedule
How often should maintenance tasks be performed? - - - - - - - - - - - - - 10-6
Tools required
Standard GE tool kit - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-8
GE-2 tool kit - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-10
Special tools, supplies and equipment used for maintenance - - - - - - 10-11
System maintenance
Preliminary checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-12
Functional checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-13
Physical inspection - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-15
Optional Diagnostic Checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-16
Probe maintenance- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-17
Battery Performance Maintenance - - - - - - - - - - - - - - - - - - - - - - - - - 10-19
Electrical safety tests
Safety test overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-20
Leakage current limits - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-22
Outlet test - wiring arrangement - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-24
Grounding continuity - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-25
Chassis leakage current test - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-26
Probe leakage current test- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-28
When there's too much leakage current …
AC/DC Fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-31
Chassis Fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-31
Probe Fails- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-32
Peripheral Fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-32
Still Fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-32
New Unit - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-32
ECG Fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-32

5610739-100 English Rev.10
Inspection Paperwork
Ultrasound Inspection Forms - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-33
Electrical Safety Tests Log
Index

5610739-100 English Rev.10
5610739-100 English Rev.10
Chapter 1
Introduction
This chapter describes important issues related to

safely servicing the Ultrasound system. The service
provider must read and understand all the information
presented here before installing or servicing the units.
LOGIQ V2/LOGIQ V1 – Basic Service Manual 1-1

5610739-100 English Rev.10
Introduction
Overview
Contents in this chapter

• ‘Overview’ on page 1-2
• ‘Manual Overview’ on page 1-3
• ‘Important conventions’ on page 1-6
• ‘Product icons’ on page 1-10
• ‘Labels locations’ on page 1-11
• ‘Safety considerations’ on page 1-13
• ‘Dangerous procedure warnings’ on page 1-22
• ‘Lockout/Tagout (LOTO) requirements’ on page 1-23
• ‘Returning probes and repair parts’ on page 1-24
• ‘EMC, EMI and ESD’ on page 1-25
• ‘Customer assistance’ on page 1-27
1-2 LOGIQ V2/LOGIQ V1 – Basic Service Manual

5610739-100 English Rev.10
Manual Overview
Manual Overview
This manual provides installation and service information for the

LOGIQ V2/LOGIQ V1 Ultrasound system. It is divided in ten
chapters as shown below.
Contents in this manual

The manual is divided into ten chapters.
In the beginning of the manual, before chapter 1, you will find
the Revision overview, the Important precautions including
Translation policy, Damage in transportation, Certified electrical
contractor statement, Omission & errors, Service safety
considerations and Legal notes, and the Table of Contents
(TOC).
An Index has been included after Chapter 10.
Table 1-1: Contents in this manual
Chapter Chapter title Description

number
1. Introduction Contains a content summary and warnings.
2. Site preparations Contains pre-setup requirements for the LOGIQ
V2/LOGIQ V1.
3. System Setup Contains setup procedure with procedure
checklist for the system.
4. General Procedures Contains functional checks that must be
and Functional performed as part of the installation, or as
Checks required during servicing and periodic
maintenance.
5. Components and Contains block diagrams and functional
Functions (Theory) explanations of the electronics.
6. Service Adjustments Contains instructions on how to make any
available adjustments to the LOGIQ V2/LOGIQ
V1.

5610739-100 English Rev.10
Introduction
Table 1-1: Contents in this manual (Continued)
Chapter Chapter title Description

number
7. Diagnostics/ Provides procedures for running diagnostic or
Troubleshooting related routines for the LOGIQ V2/LOGIQ V1.
8. Replacement Provides disassembly procedures and
procedures reassembly procedures for all changeable FRU.
9. Renewal Parts Contains a complete list of replacement parts for
LOGIQ V2/LOGIQ V1.
10. Care & Maintenance Provides periodic maintenance procedures for
LOGIQ V2/LOGIQ V1.
N/A Index A quick way to the topic you’re looking for.
Typical users of the Proprietary Service Manual

• GEHC Service Personnel (setup, maintenance, etc.)
• GEHC Online Center Personnel
• Licensed Hospital’s Service Providers

5610739-100 English Rev.10
Manual Overview
LOGIQ V2/LOGIQ V1 models covered by this manual
Table 1-2: LOGIQ V2/LOGIQ V1 Model Designations
Model Number Description System SW
5661244 LOGIQ V2 Generic version R1.x.x
5661242 LOGIQ V1 Generic version R1.x.x
NOTE: When not otherwise specified, the contents of this manual

applies to all LOGIQ V2/LOGIQ V1 models.

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Introduction
Conventions used in book

Important conventions, used in this document, are described
next.
Model designations
This manual covers the LOGIQ V2/LOGIQ V1 Ultrasound

systems listed in:
‘LOGIQ V2/LOGIQ V1 models covered by this manual’ on
page 1-5.
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.

5610739-100 English Rev.10
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
personnel are labeled in one of three ways:
• DANGER
• WARNING
• CAUTION
DANGER Danger is used to indicate the presence of a hazard that will

cause severe personal injury or death if the instructions are
ignored.
WARNING Warning is used to indicate the presence of a hazard that can

cause severe personal injury and property damage if
instructions are ignored.
CAUTION Caution is used to indicate the presence of a hazard that will or

can cause minor personal injury and 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.

5610739-100 English Rev.10
Introduction
Standard hazard icons

Important information will always be preceded by either 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 possibly 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
ELECTRICAL
MECHANICAL
RADIATION
LASER
HEAT
PINCH
NOTE: Even if a symbol isn’t used on the product or in this manual, it

may be included for your reference.

5610739-100 English Rev.10
Standard Icons that indicate that a special procedure is to be used
Some others icons make you aware of specific procedures that

should be followed.
Table 1-4: Standard Icons that indicates that a special procedure is to be used
Avoid Static Electricity Tag and Lock Out Wear Eye Protection
Hand Protection Foot Protection Wear Eye Protection
Be sure to read the notes; the information contained in a note

can often save you time or effort.

5610739-100 English Rev.10
Introduction
Product icons
It is important to refer to the current revision of the Ultrasound

system’s User Manual for a full list of product labels prior to
servicing the system.

5610739-100 English Rev.10
Labels locations
Labels locations
It is important to refer to the current revision of the Ultrasound

system’s User Manual for a full list of product labels prior to
servicing the system.
LOGIQ V2/LOGIQ V1 labels are provided in English.
The labels are at the bottom of the system. The label content
may be different for different regions and systems. Please refer
to the labels on the system for the actual content
Figure 1-1. LOGIQ V1 Label Location
Figure 1-2. LOGIQ V2 Label Location
1. Rating Plate

5610739-100 English Rev.10
Introduction
Table 1-5: Label Icons
Label/Icon Purpose/Meaning Location
Every system has a unique Rating plate

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 LOGIQ V2/LOGIQ V1 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.
Serial Number. Rating plate

5610739-100 English Rev.10
Contents in this section

• ‘Introduction’ on page 1-13
• ‘Human Safety’ on page 1-13
• ‘Mechanical safety’ on page 1-16
• ‘Electrical safety’ on page 1-18
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.
Human Safety
• Operating personnel must not remove the system covers.
• Servicing should be performed by authorized personnel
only.
Only personnel who have participated in a LOGIQ V2/LOGIQ V1
Training Seminar are authorized to service the equipment.
DANGER DANGEROUS VOLTAGES, CAPABLE OF CAUSING

DEATH, ARE PRESENT IN THIS EQUIPMENT. USE
EXTREME CAUTION WHEN HANDLING, TESTING
AND ADJUSTING.
WARNING If the covers are removed from an operating LOGIQ V2/LOGIQ

V1, some metal surfaces may be warm enough to pose a
potential heat hazard if touched, even while in shutdown mode.

5610739-100 English Rev.10
Introduction
Human Safety (continued)
WARNING 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.
WARNING DO NOT substitute parts or modify equipment

Because of the danger of introducing additional hazards, ONLY
install GE approved parts. DO NOT perform any unauthorized
modification of the equipment.
WARNING Ensure that the Ultrasound system is turned off and unplugged
Wait for at least 20 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.
Ultrasound system components may be energized. Always
refer to the Ultrasound system's Proprietary Service Manual for
LOTO warnings and cautions
WARNING 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 20 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.
Ultrasound System components may be energized. Always
refer to the Ultrasound system's Proprietary Service Manual for
LOTO warnings and cautions

5610739-100 English Rev.10
Human Safety (continued)
WARNING Use all Personal Protection Equipment (PPE) such as gloves,

safety shoes, safety glasses, and kneeling pad, to reduce the
risk of injury.
WARNING 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.
WARNING Wear all PPE including gloves as indicated in the chemical

MSDS.

5610739-100 English Rev.10
Introduction
Mechanical safety
WARNING While the software install procedure is designed to preserve

data, you should save any patient data, images, system setups
to removable media or hardcopy before doing a software
upgrade.
WARNING Ultrasound probes are highly sensitive medical instruments

that can easily be damaged by improper handling. Use care
when handling and protect from damage when not in use. Do
NOT use a damaged or defective probe. Failure to follow these
precautions can result in serious injury and equipment
damage.
WARNING Never use a probe that has fallen to the floor. Even if it looks
OK, it may be damaged.
CAUTION The LOGIQ V2/LOGIQ V1 system weights 6 kg or more,

depending on installed peripherals, when ready for use. To
avoid possible injury and equipment damage when
transporting from one area of use to another:
• Use the handle to move the Ultrasound system.
• Do not let the Ultrasound system strike walls or door frame.
NOTE: Special care should be taken when transporting the Ultrasound

system in a vehicle:
• Before transporting, place the system in its special storage
case.
• Ensure that the system is firmly secured while inside the
vehicle.
• Secure 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.

5610739-100 English Rev.10
Mechanical safety (continued)
WARNING When the Ultrasound system is raised for a repair or moved

along any incline, use extreme caution since it may become
unstable and tip over.
CAUTION Use protective glasses during drilling, filing smooth surfaces,

and during all other work where eyes need protection.
CAUTION Use safety shoes when doing work where there is any chance
of foot injury.
CAUTION Use protective gloves when working with sharp edges or when
directed to wear PPE during a removal/replacement procedure.
CAUTION Be careful not to pinch any of the cables.

5610739-100 English Rev.10
Introduction
Electrical safety
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 system power cable and the power connector must
meet international electrical standards
WARNING Connecting a LOGIQ V2/LOGIQ V1 to the wrong voltage level

will most likely destroy it.

5610739-100 English Rev.10
Probes
Follow these guidelines before connecting a probe to the

Ultrasound system:
• 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.
Peripherals
Refer to the Patient Safety Environment section of the User’s

Manual for peripheral isolation information.

5610739-100 English Rev.10
Introduction
Battery Safety
To avoid the risk of injury, follow the warning and cautions to
make sure that the battery does not burst, ignite, or generate
heat of fumes.
WARNING • The battery has a safety device. Do not disassemble or

alter the battery.
• Charge and discharge the batteries only when the ambient
temperature is between 10° and 40° C (50° F and 104° F).
• Do not short-circuit the battery by directly connecting the
negative terminals with metal objects.
• Do not heat the battery or discard it in a fire.
• Do not expose the battery to temperature over 50° C
(122° F). Keep it away from fire and other heat sources.
• Do not charge the battery near a heat source, such as a
fire or heater.
• Do not leave the battery in direct sunlight.
• Do not drop packs from height to prevent them from
possible malfunction damage.
• Do not drop packs from height to prevent them from
possible malfunction damage.
• Do not pierce the battery with a sharp object, hit it, or step
on it.
• Do not use a damaged battery.
• Do not solder a battery.
• Do not connect the battery to an electrical power outlet.
• Do not contact PCM (Power Control and Monitor, it’s a
small board in the battery) directly to prevent packs from
ESD damage.
• In case of longer non-use of the LOGIQ V2/LOGIQ V1,
please make sure the battery is removed.

5610739-100 English Rev.10
Battery Safety (continued)
CAUTION To avoid the battery bursting, igniting, or fumes from the

battery causing equipment damage, observe the following
precautions:
• Do not immerse the battery in water or allow it to get wet.
• Do not put the battery into a microwave oven or
pressurized container.
• If the battery leaks or emits an odor, remove it from all
possible flammable sources.
• If the battery emits an odor or heat, is deformed or
discolored, or in a way appears abnormal during use,
recharging or storage, immediately remove it and stop
using it. If you have any questions about the battery,
consult GE or your local representative.
• Short term (less than one month) storage of battery pack:
• Store the battery in a temperature range between-5° C
(23° F) and 50° C (122°F).
• Use only GE recognized batteries.
• In case of the long term (3 months or more) storage:
• Store the battery in a temperature range of -5° C (23°
F) and 50° C (122°F).
• When charging for the first time after long-term
storage. Recover such packs to original performance
through repeating several cycles of full charging and
discharging.
• When store packs for more than 6 months, charge at
lease once charging require per 6 months to prevent
leakage and deterioration in performance due to
self-discharging.
• When the system isn't powered on continuously more than
6 months, in order to prevent leakage and deterioration in
performance of CMOS battery, power on the system at
least once per 6 months for more than 10 hours to have
CMOS battery fully charged. Time and date need to be
re-setup.
NOTE: The battery shall be shipped in about 30% charged state. Those
packs have to be fully charged and discharged up to 3 times to
utilize Li-lon smart packs before use.

5610739-100 English Rev.10
Introduction
Dangerous procedure warnings
Warnings, such as the example below, precede potentially

dangerous procedures throughout this manual. Instructions
contained in the warnings must be followed.
DANGER DANGEROUS VOLTAGES, CAPABLE OF CAUSING

DEATH, ARE PRESENT IN THIS EQUIPMENT. USE
EXTREME CAUTION WHEN HANDLING, TESTING
AND ADJUSTING.
WARNING If the covers are removed from an operating LOGIQ V2/LOGIQ

V1, some metal surfaces may be warm enough to pose a
potential heat hazard if touched, even while in shutdown mode.
WARNING 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.
WARNING DO NOT substitute parts or modify equipment

Because of the danger of introducing additional hazards, ONLY
install GE approved parts. DO NOT perform any unauthorized
modification of the equipment.
WARNING SHUT DOWN FORCEDLY OR PLUG IN/OUT ACDC

INVALID MAY CAUSE THE DAMAGE OF SYSTEM
FILES.

5610739-100 English Rev.10
Lockout/Tagout (LOTO) requirements
Lockout/Tagout (LOTO)
requirements
Follow Lockout/Tagout requirements by ensuring you are in total

control of the AC power plug at all times during the service
process.
To apply Lockout/Tagout (LOTO):
1. Plan and prepare for shutdown.
2. Shutdown the equipment.
3. Isolate the equipment.
4. Remove/disconnect the battery, if present.
5. Apply Lockout/Tagout Devices.
6. Control all stored and residual energy.
7. Verify isolation.
All potentially hazardous stored or residual energy is relieved.
WARNING Energy Control and Power Lockout for LOGIQ V2/LOGIQ V1.
When servicing parts of the Ultrasound 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 Ultrasound system.
4. Maintain control of the Ultrasound system power plug.
5. Wait for at least 30 seconds for capacitors to discharge as
there are no test points to verify isolation.
Ultrasound System components may be energized.

5610739-100 English Rev.10
Introduction
Returning 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 Ultrasound system is not meant to be used for long-term
storage of patient data or images. The user is responsible for the
data on the system and a regular backup is highly
recommended.
If the system is sent for repair, please ensure that any patient
information is backed up and erased from the system 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.

5610739-100 English Rev.10
EMC, EMI and ESD
EMC, EMI and ESD
What is 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
interference from its environment or when the device produces
unacceptable levels of emission to its environment. 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 of
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.
CE Compliance
LOGIQ V2/LOGIQ V1 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.
For applicable standards, refer to the Safety Chapter of the
Ultrasound system User’s Manual.
NOTE: For CE Compliance, it is critical that all covers, screws,
shielding, gaskets, mesh, clamps, are in good condition,
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.

5610739-100 English Rev.10
Introduction
Electrostatic discharge (ESD) prevention
WARNING DO NOT touch any boards with integrated circuits prior to

taking the necessary ESD precautions.
Always connect yourself, via an arm-wrist strap, to the advised
ESD connection point located on the rear of the Ultrasound
system (near the power connector).
Follow general guidelines for handling of electrostatic sensitive
equipment.
WARNING Risk of electrical shock, Ultrasound 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.

5610739-100 English Rev.10
Customer assistance
Customer assistance
Contact information
If this equipment does not work as indicated in this service
manual or in the user manual, or if you require additional
assistance, please contact the local distributor or appropriate
support resource, as listed below.
Before you call, identify the following information, and acquire
image (Alt+D) to send to the Customer Care team:
1. System ID serial number.
2. Software version.
3. Date and time of occurrence.
4. Sequence of events leading to issue.
5. Is the issue repeatable?
6. Imaging mode, probe, preset/application.
7. Media brand, speed, capacity, type.
8. Save secondary image capture, cine loop.
NOTE: Restart the application before resuming clinical scanning.
NOTE: The serial number can be found at the bottom of the system.

5610739-100 English Rev.10
Introduction
Phone numbers for Customer Assistance

Table 1-6: Phone numbers for Customer Assistance
LOCATION PHONE NUMBER
USA Service: On-site 1-800-437-1171

GE Healthcare - GE Medical Systems
Ultrasound Service Engineering Service Parts 1-800-558-2040
9900 Innovation Drive
Application Support 1-800-682-5327 or
Wauwatosa, WI 53226
1-262-524-5698
Canada Phone: 1-800-668-0732
Latin America Service 1-800-321-7937

Application Support 1-262-524-5698
Europe (OLC-EMEA) OLC - EMEA

GE Ultraschall Deutschland Gmbh & Co. KG Phone: +49 (0) 212 2802 - 652
Beethovenstraße 239 +33 1 3083 1300
Postfach 11 05 60, D-42655 Solingen
Germany Fax: +49 (0) 2122-8024-31
Online Services Ultrasound Asia Phone:

• Australia +(61) 1-800-647-855
• China +(86) 800-810-8188
• India +(91) 1800-425-8025
• Japan +(81) 42-648-2940
• Korea +(82) 2620 13585
• Singapore +(95) 6277-3444
System manufacturer
Table 1-7: System manufacturer
MANUFACTURER PHONE NUMBER FAX NUMBER
GE Medical Systems (China) Co., Ltd. +86 510 85225888 +86 510 85226688
No.19 Changjiang Road
WuXi National Hi-Tech Development Zone
Jiangsu
P.R.China 214028

5610739-100 English Rev.10
Customer assistance
Authorized Representative
Table 1-8: Authorized Representative
TELEPHONE / FAX
AUTHORIZED REPRESENTATIVE NUMBER
The location of the CE marking is shown in the Safety chapter of the User +49 761 45 43 -0 /
manual. +49 761 45 43 -233
Authorized EU Representative/European registered place of business:

GE Medical Systems Information Technologies GmbH (GEMS IT GmbH)
Munzinger Strasse 5, D-79111 Freiburg, GERMANY

5610739-100 English Rev.10
Introduction

5610739-100 English Rev.10
Chapter 2
Site Preparations
This chapter provides the information required to plan

and prepare for the setup of an Ultrasound system.
Included are descriptions of the facility and electrical
needs to be met by the purchaser of the units.

5610739-100 English Rev.10
Site Preparations
Overview

• ‘General Ultrasound system requirements’ on page 2-3
• ‘Facility needs’ on page 2-12
• ‘Environmental Dangers’ on page 2-22

5610739-100 English Rev.10
General Ultrasound system

requirements

• ‘Ultrasound system environmental requirements’ on
page 2-3
• ‘Electrical requirements’ on page 2-6
• ‘EMI limitations’ on page 2-9
• ‘Probes environmental requirements’ on page 2-11
• ‘Time and manpower requirements’ on page 2-11
Ultrasound system environmental requirements
If the Ultrasound system is very cold or hot
When unpacking the Ultrasound system, allow the temperature

of the Ultrasound system to stabilize before powering up. The
following table describes guidelines for reaching operational
temperatures from storage or transport temperatures.
CAUTION If the Ultrasound system is very cold or hot, do not turn on its
power until it has had a chance to acclimate to its operating
environment.
Table 2-1: System Acclimation Time Chart
Degree C 50 45 40 35 30 25 20 15 10 5 0 -5
Degree F 122 113 104 95 86 77 68 59 50 41 32 23
hours 4 2 0 0 0 0 0 0 0 2 4 6

5610739-100 English Rev.10
Site Preparations
Environmental specifications for Ultrasound system
The system should be operated, stored, or transported within

the parameters outlined below. Either its operational
environment must be constantly maintained or the unit must be
turned off.
Table 2-2: System Environmental Requirements
Operational Storage Transport (<16hrs.)
Temperature 10° - 40°C -5° - 50°C -5° - 50°C

50° - 104°F 23° - 122°F 23° - 122°F
Humidity 30 - 80% 10 - 90% 10 - 90%

non-condensing non-condensing non-condensing
Pressure 700 - 1060hPa 700 - 1060hPa 700 - 1060hPa
CAUTION Ensure that the probe face temperature does not exceed the
normal operation temperature range.
CAUTION The LOGIQ V2/LOGIQ V1 system and probe connector is not

waterproof. Do not expose the device to water or any kind of
liquid.

5610739-100 English Rev.10
Cooling
The cooling requirement for a console Ultrasound system with

monitor and on board peripherals, is up to 3800 BTU/h. This
figure does not include cooling needed for lights, people, or
other equipment in the room.
NOTE: Each person in the room places an additional 300 BTU/h
demand on the cooling system.
Lighting
Bright light is needed for Ultrasound system installation, updates

and repairs. However, operator and patient comfort may be
optimized if the room light is subdued and indirect. Therefore a
combination lighting system (dim/bright) is recommended. Keep
in mind that lighting controls and dimmers can be a source of
EMI which could degrade image quality. These controls should
be selected to minimize possible interference.

5610739-100 English Rev.10
Site Preparations
Electrical requirements
General requirements
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.
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 system is only a conduit.
Electrical requirements for the Ultrasound system
In the table below, the electrical specifications for the Ultrasound

system includes monitor and on board peripherals.
Table 2-3: Electrical Specifications for LOGIQ V2/LOGIQ V1 system
Voltage Tolerance Power Consumption Frequency
100-240 VAC ±10% Max. 200VA 50/ 60HZ

5610739-100 English Rev.10
Site circuit breaker
CAUTION Power outage may occur. The LOGIQ V2/LOGIQ V1 requires a

dedicated single branch circuit. To avoid circuit overload and
possible loss of critical care equipment, make sure you do not
have any other equipment operating on the same circuit.
It is recommended that the branch circuit breaker for the

Ultrasound system be readily accessible.
CAUTION POWER OUTAGE MAY OCCURE.

The LOGIQ V2/LOGIQ V1 requires a dedicated single branch
circuit. To avoid circuit overload and possible loss of critical
care equipment, make sure you DO NOT have any other
equipment operating on the same circuit.
Site power outlets
A dedicated AC power outlet must be within reach of the

Ultrasound system without extension cords. Other outlets
adequate for the external peripherals, medical and test
equipment needed to support this Ultrasound system must also
be present within 1 m (3.2 ft.) of the Ultrasound system.
Electrical installation must meet all current local, state, and
national electrical codes.
Unit power plug
If the Ultrasound system arrives without a power plug, or with

the wrong plug, you must contact your GE dealer or the
installation engineer must supply what is locally required.

5610739-100 English Rev.10
Site Preparations
Power stability requirement
Table 2-4: Power stability requirement
IEC 61000-4-11 < 5%T (> 95% dip) for < 5%T (> 95% dip) for Mains power
0.5 cycle; 0.5 cycle; quality should be
Voltage dips, short
interruptions and 40%T (60% dip) for 5 40%T (60% dip) for 5 that of a typical
voltage variations cycles; cycles; commercial or
on mains supply hospital
70%T (30 dip) for 25 70%T (30 dip) for 25
cycles; cycles;
environment.
< 5%T (>95% dip) for 5 < 5%T (>95% dip) for 5
sec sec

5610739-100 English Rev.10
EMI limitations
Ultrasound systems are susceptible to Electromagnetic
Interference (EMI) from radio frequencies, magnetic fields, and
transients in the air or wiring. They also generate EMI. The
Ultrasound system complies with limits as stated on the EMC
label. However there is no guarantee that interference will not
occur in a particular installation.
Possible EMI sources should be identified before the Ultrasound
system is installed.
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.
See: ‘EMI prevention/abatement’ on page 2-10 for EMI
prevention tips.

5610739-100 English Rev.10
Site Preparations
EMI prevention/abatement
Table 2-5: EMI prevention/abatement
EMI RULE DETAILS
Be aware of Radio • Keep the Ultrasound system at least 5 meters (15 feet) away from other EMI
Frequency sources sources.
• Special shielding may be required to eliminate interference problems caused by
high frequency, high powered radio or video broadcast signals.
Ground the Poor grounding is the most likely reason an Ultrasound system will have noisy
Ultrasound system images. Check grounding of the power cord and power outlet.
Replace all screws, • After you finish repairing or updating the Ultrasound system, replace all covers
Radio Frequency and tighten all screws.
gaskets, covers, • Any cable with an external connection requires a magnet wrap at each end.
cores • Install all covers. Loose or missing covers or Radio Frequency gaskets allow
radio frequencies to interfere with the ultrasound signals.
Replace broken If more than 20% or a pair of the fingers on an Radio Frequency gasket are
Radio Frequency broken, replace the gasket. Do not turn on the Ultrasound system until any loose
gaskets metallic part is removed.
Do not place labels Where applicable, never place a label where Radio Frequency gaskets meet the
where Radio Ultrasound system. Otherwise, the gap created will permit Radio Frequency
Frequency gaskets leakage. Or, if a label has been found in such a position, move the label.
touch metal
Use GE specified The interconnect cables are grounded and require ferrite beads and other
harnesses and shielding. Also, cable length, material, and routing are all important; do not change
peripherals from what is specified.
Take care with Cellular phones may transmit a 5 V/m signal; that could cause image artifacts.
cellular phones
Properly route Where applicable, do not allow cables to lie across the top of the Card Rack or
peripheral cables hang out of the peripheral bays. Loop the excess length for peripheral cables
inside the peripheral bays. Attach the monitor cables to the frame.

5610739-100 English Rev.10
Probes environmental requirements
Operation, storage and transport temperatures for probes
Probes should be operated, stored, or transported within the

parameters outlined below.
Table 2-6: Probe Environmental Requirements
Operational Storage Transport
Temperature 10° - 40° C -5° - 50° C -5° - 50° C

50° - 104° F 23° - 122° F 23° - 122° F
Humidity 30- 80% 10 - 90% 10 - 90%

non-condensing non-condensing non-condensing
Pressure 700 - 1060hPa 700 - 1060hPa 700 - 1060hPa
CAUTION Check the room temperature before you use the probe.
NOTE: Refer to Table 2-1 on page 2-3 to determine the needed

settlement time.
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.

5610739-100 English Rev.10
Site Preparations
Facility needs

• ‘Purchaser responsibilities’ on page 2-13
• ‘Required facility needs’ on page 2-14
• ‘Desirable features’ on page 2-15
• ‘Minimal floor plan suggestion’ on page 2-16
• ‘Recommended floor plan suggestion’ on page 2-17
• ‘Suggested floor plan, Ultrasound system, and EchoPAC PC
in same room’ on page 2-18
• ‘Networking setup requirements’ on page 2-19

5610739-100 English Rev.10
Facility needs
Purchaser responsibilities
The work and materials needed to prepare the site is the
responsibility of the purchaser. Delay, confusion, and waste of
manpower can be avoided by completing pre-installation work
before delivery. Purchaser responsibility includes:
• Procuring the materials required
• Completing the preparations before delivery of the
Ultrasound system
• Paying the costs for any alterations and modifications not
specifically provided 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.

5610739-100 English Rev.10
Site Preparations
Required facility needs

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.
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.

5610739-100 English Rev.10
Facility needs
Required facility needs (continued)

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.
• Dedicated single branch power outlet of adequate
amperage meeting all local and national codes which is
located less than 2.5 m (8 ft.) from the unit’s proposed
location
• Door opening is at least 76 cm (30 in) wide
• Proposed location for unit is at least 0.5m (1.5 ft.) from the
wall for cooling
• Power outlet and place for any external peripheral are within
2 m (6.5 ft.) of each other with peripheral within 1 m of the
unit to connect cables.
• Power outlets for other medical equipment.
• Power outlets for test equipment within 1 m (3.2 ft.) of
Ultrasound system.
• Clean and protected space to store probes (in their cases or
on a rack)
• Material to safely clean probes (done with a plastic
container, never metal)
For the amperage requirements, see: ‘Electrical requirements’
on page 2-6.
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

5610739-100 English Rev.10
Site Preparations
Minimal floor plan suggestion

CSI 8x10
Scale:
Each square equals one square
4 5 foot (app. 31 x 31 cm)
2 3
11
10
9
8 12
13
7
6 14
1
1. Door – at least 762 mm (30 6. Examination Table – 1930 x 12. Network Interface
inches) 610 mm (76 x 24 inches) 13. 457 mm (18 inches) distance
2. Film Viewer 7. Footswitch of Ultrasound system from
3. Counter Top, Sink with hot 8. Stool wall or objects
and cold water and Supplies 9. Ultrasound system 14. GE Cabinet for Software and
Storage 10. External Peripherals Manuals
4. Linen Supply 11. Dedicated Power Outlet -
5. Probes/Supplies Circuit Breaker protected and
easily accessible
Figure 2-1. Minimal floor plan, 2.5 m x 3 m (8 by 10 foot)

5610739-100 English Rev.10
Facility needs
Recommended floor plan suggestion

CSI 14x17
10 11 15
12
13 14 16
2 3 4 5
7
1
17
18
Scale: Each square equals one square foot (app. 31 x 31 cm)
1. Secretaries or Doctors Desk 8. Suction Line 14. Footswitch

2. File Cabinet 9. Ultrasound system 15. Storage for Linens and
3. Film Viewer 10. Dedicated Power Outlet - Equipment
4. Counter Top Circuit Breaker protected and 16. Examination Table – 1930 x
5. Counter Top and Sink with easily accessible 610 mm (76 x 24 inches)
hot and cold water 11. Network Interface 17. Lavatory and Dressing Room
6. Overhead Lights Dimmer - 12. 457 mm (18 inches) distance 18. Door – at least 762 mm (30
Dual Level Lighting (bright of Ultrasound system from inches)
and dim) wall or objects
7. Emergency Oxygen 13. Stool
Figure 2-2. A 14 by 17 foot recommended floor plan

5610739-100 English Rev.10
Site Preparations
Suggested floor plan, Ultrasound system, and EchoPAC PC in same

room
1. EchoPAC PC workstation 4. 3x mains power outlets 7. Ethernet network wall outlet

parts 5. Hot and Cold water
2. UPS 6. Dedicated mains power out-
3. Ethernet network wall outlet let
Figure 2-3. Suggested Room with EchoPAC PC workstation and Ultrasound Scanner

5610739-100 English Rev.10
Facility needs
Networking setup requirements
Stand alone Ultrasound system (without network connection)
None.
Scanner connected to hospital’s network
Supported networks:
100/1000 Mbit Ethernet/DICOM network
Wireless LAN
InSite requirements
InSite requires an Ethernet connection via:

• 100/1000 Mbit Interface
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
workstations for viewing or transferring images to remote
printers.
As an added benefit, transferring images in this manner frees up
the on-board monitor and peripherals, enabling viewing to be
done while scanning continues.
With DICOM, images can be archived, stored, and retrieved
faster, easier, and at a lower cost.

5610739-100 English Rev.10
Site Preparations
DICOM option setup requirements
To configure the Ultrasound system to work with other network

connections, the site’s network administrator must provide
information to complete the form “Worksheet for DICOM
Network Information”. Ensure that there are no spaces in any
field of the form.
See:
Entries must include:
• A host name, local port number, AE Title, IP address and
Net Mask for the Ultrasound system.
• The IP addresses for the default gateway and other routers
at the site for ROUTING INFORMATION.
• The host name, IP address, port and AE Title for each
device the site wants connected to the Ultrasound system
for DICOM APPLICATION INFORMATION. A field for the
make (manufacturer) and the revision of the device, is also
included. This information may be useful for error solving.

5610739-100 English Rev.10
Facility needs
DICOM option setup requirements (continued)
Figure 2-4. Worksheet for DICOM Network Information

5610739-100 English Rev.10
Site Preparations
Environmental Dangers
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 providing the device with extra protective earth, will be required
in order to meet IEC60601-1 standards for electrical leakage.
Patient Environment IEC60601-1 and ANSI AAMI ES60601-1
Sub Clause 3.79 and figure A.9 (IEC60601-1:2005 and ANSI AAMI
ES60601-1:2005)
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
ENVIROMENT.
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 will be depicted as a dashed line in this procedure.
See example below.
1. Patient environment
Figure 2-5. Patient environment

5610739-100 English Rev.10
Chapter 3
System Setup
This chapter contains information needed to install

LOGIQ V2/LOGIQ V1 system.
Included is a procedure that describes how to receive

and unpack the equipment and how to file a damage or
loss claim.
How to prepare the facility and unit of the actual

installation, and how to check and test the unit, probes,
and external peripherals for electrical safety are also
included in this procedure.

5610739-100 English Rev.10
System Setup
Overview

• ‘Setup reminders’ on page 3-3
• ‘Receiving and unpacking the equipment’ on page 3-6
• ‘Preparing for setup’ on page 3-13
• ‘Completing the setup’ on page 3-14
• ‘System Configuration’ on page 3-18
• ‘Peripherals Installation Instructions’ on page 3-22
• ‘Connectivity setup’ on page 3-34
• ‘Paperwork after setup’ on page 3-42

5610739-100 English Rev.10
Setup reminders
Setup reminders
Average setup time

• Unpacking the LOGIQ V2/LOGIQ V1: 20 minutes
• Set up LOGIQ V2/LOGIQ V1 options: 15 minutes
• DICOM Network Configuration: 30 minutes or more,
depending on the configuration
• Install Insite: 0.5 hour
The LOGIQ V2/LOGIQ V1 installation and functional checkout
will take approximately one hour. LOGIQ V2/LOGIQ V1
consoles with optional equipment may take slightly longer.
Setup warnings
DANGER WHEN USING ANY TEST INSTRUMENT THAT IS CAPABLE

OF OPENING THE AC GROUND LINE (I.E., METER’S
GROUND SWITCH IS OPEN), DON’T TOUCH THE
ULTRASOUND SYSTEM!
CAUTION To prevent electrical shock, connect the unit to a properly

grounded power outlet. DO NOT use a three to two prong
adapter. This defeats safety grounding.
CAUTION DO NOT wear the ESD wrist strap when you work on live
circuits and more than 30 V peak is present.
CAUTION DO NOT operate this unit unless all board covers and frame
panels are securely in place. System performance and cooling
require this.

5610739-100 English Rev.10
System Setup
Setup warnings (continued)

1. There are no operator serviceable components. To prevent
shock, do not remove any covers or panels. Should
problems or malfunctions occur, unplug the power cord.
Only qualified service personnel should carry out servicing.
NOTE: For information regarding packing labels, refer to LABELS
ON PACKAGE.
2. After being transported, the unit may be very cold or hot. If
this is the case, allow the unit to acclimate before you turn it
on. It requires one hour for each 2.5°C increment it's
temperature is below 3°C or above 40°C.
DANGER Equipment damage possibility. Turning the system on without

acclimation after arriving at site may cause the system to be
damaged.
CAUTION If the Ultrasound system is very cold or hot, do not turn on its power
until it has had a chance to acclimate to its operating environment.
The following table describes guidelines for reaching operational

temperatures from storage or transport temperatures.
Table 3-1: System Acclimation Time Chart
Degree C 50 45 40 35 30 25 20 15 10 5 0 -5
Degree F 122 113 104 95 86 77 68 59 50 41 23 23
hours 4 2 0 0 0 0 0 0 0 2 4 6

5610739-100 English Rev.10
Setup reminders
Setup warnings (continued)
CAUTION Operator Manual(s)

The User Manual(s) should be fully read and understood
before operating the LOGIQ V2/LOGIQ V1 and kept near the
Ultrasound system for quick reference.
CAUTION Acoustic Output Hazard

Although the ultrasound energy transmitted from the LOGIQ
V2/LOGIQ V1 probe is within AIUM/NEMA standards, avoid
unnecessary exposure. ultrasound energy can produce heat
and mechanical damage.

5610739-100 English Rev.10
System Setup
Receiving and unpacking the

equipment
Purpose of this section

This section describes how to receive and unpack the
LOGIQ V2/LOGIQ V1.

• ‘Warnings for receiving and unpacking’ on page 3-6
• ‘Receiving the LOGIQ V2/LOGIQ V1’ on page 3-6
• ‘Unpacking the LOGIQ V2/LOGIQ V1’ on page 3-8
Warnings for receiving and unpacking
CAUTION Remember to use relevant personal protecting equipment

(PPE) during packing and unpacking. Check with your local
EHS representative.
Receiving the LOGIQ V2/LOGIQ V1
Overview
Improper handling during transportation may harm the

equipment inside the package even if the package itself is
undamaged.
Examine all packages
Examine package closely at time of delivery, as described in the

procedure below.

5610739-100 English Rev.10
Damage in transportation
Follow this procedure if damage is apparent:

1. 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.
2. Report the damage to the carrier.
• 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.

5610739-100 English Rev.10
System Setup
Unpacking the LOGIQ V2/LOGIQ V1

When a new system arrives, check that any components are not
damaged and are not in short supply. If shipping damage or
shortage occurs, contact the address shown in Chapter 1
CAUTION Please carefully unpack the system, and do not dispose the
package of LOGIQ V2/LOGIQ V1, so that it can be reused for
service.
NOTE: Please check the LOGIQ V2/LOGIQ V1 console is well

assembly after unpacking the system.
1. Cut the adhesive tape and open top covers of paper carton.
Figure 3-1. Open Top Covers of Paper Carton

5610739-100 English Rev.10
Unpacking the LOGIQ V2/LOGIQ V1 (continued)

2. Take out console together with 2 interleavers from console
package.
3. Take out the interleavers beside Accessories Package
4. Take out Accessories Package.
Figure 3-2. Unpacking the equipment
CAUTION Do not lift the unit by the rubber band. Equipment damage
may result.

5610739-100 English Rev.10
System Setup

5. Remove 2 interleavers.
6. Remove plastic bag.
Figure 3-3. Removing interleavers and plastic bag

5610739-100 English Rev.10

NOTE: Check the shipping container for special instructions. Verify that
the container is intact. In some cases a secondary container
may be used. If so, ask the carrier for unpacking instructions.
Figure 3-4. Labels on Package
Moving into Position
CAUTION Do not lift the unit by the rubber band. Use handle to move
system.
CAUTION Equipment Damage Possibility. Lifting the console by holding

covers may damage the covers. Do not lift the console by
holding any covers.
In general, a single adult can move the LOGIQ V2/LOGIQ V1.

Before moving, store all loose parts in original accessory box or
in back pack. Return probes to original box.
Packing the Equipment

Please pack LOGIQ V2/LOGIQ V1 in the reverse order of
unpacking.

5610739-100 English Rev.10
System Setup
Packing materials - recycling

information
The packing materials for LOGIQ V2/LOGIQ V1 are recyclable:

• The Transportation Box is made of spruce or similar
material. (“PHYTOSANITARY CERTIFICATE” included in all
shipments to The People's Republic of China.)
• Lever lockings (hinges) are made of zinc plated steel.
• The inner reinforcements are made of Ethafoam
(Polyethylene foam).
• The plastic foil is made of LDPE (Low Density
Polyethylene).

5610739-100 English Rev.10
Preparing for setup
Preparing for setup
Verify 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.
Physical inspection
Verify that the system arrived intact (visual inspection).
If the system has been damaged, please refer to ‘Damage in
transportation’ on page i-14 in the beginning of this manual.
EMI protection
The LOGIQ V2/LOGIQ V1 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.
See ‘EMI limitations’ on page 2-9 for more information about
EMI protection.

5610739-100 English Rev.10
System Setup

This section describes how to complete the installation of
LOGIQ V2/LOGIQ V1.

• ‘System specifications’ on page 3-14
• ‘Electrical specifications’ on page 3-15
• ‘Peripheral/Accessories Connector Panel’ on page 3-16
• ‘Connecting probes’ on page 3-17
• ‘Powering the system’ on page 3-17
System specifications
System requirements verification
• Verify that the site meets the requirements listed in

Chapter 2.
(See: ‘Facility needs’ on page 2-12.)
• Verify that the specifications below don’t conflict with any
on-site conditions.
Physical dimensions
Table 3-2: Physical dimensions of LOGIQ V2/LOGIQ V1
Height Length Width Unit
120 396 368 mm

4.72 15.59 14.49 Inches
Console Weight
• Weight: approx. 6 kg (13.23 lbs)

5610739-100 English Rev.10
Electrical specifications
WARNING Connecting a LOGIQ V2/LOGIQ V1 to the wrong voltage level

will most likely destroy it.
Verification of the system’s voltage setting
Verify that the mains voltage specified for the LOGIQ V2/LOGIQ
V1 is available on-site.
Refer to the latest revision of the User Manual for a full list of
product labels prior to serving the system.
Electrical specifications for LOGIQ V2/LOGIQ V1
In the table below, the electrical specifications for LOGIQ V2/

LOGIQ V1 includes monitor and on board peripherals.
Table 3-3: Electrical specifications for LOGIQ V2/LOGIQ V1
Part Power
Number Description Voltage Tolerances consumntion Frequency
5661244 LOGIQ V2 Generic

version
100-240V ±10% Max.200VA 50/60 Hz
5661242 LOGIQ V1 Generic
version

5610739-100 English Rev.10
System Setup
Peripheral/Accessories Connector Panel

LOGIQ V2/LOGIQ V1 peripherals and accessories can be
properly connected using the side connector panel.
Figure 3-5. Rear and left Side Connector Panel
1. Security Lock
2. Port for DC In (AC Adapter)
3. Composite Out Port
4. S-Video Out Port
5. HDMI Port
6. Ethernet Port
7. Isolated USB Port for AC Printer ONLY
NOTE: The AC printer can be connected to this isolated USB port
only.
8. USB Ports for Footswitch, DVD-RW, Wireless LAN Adapter,
USB Stick, USB HDD
9. SD Port

5610739-100 English Rev.10
Peripheral/Accessories Connector Panel (continued)

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. Everybody who connects additional
equipment to the signal input part or signal output part of LOGIQ
V2/LOGIQ V1, configures a medical system, and is therefore
responsible that the Ultrasound system complies with the
requirements of the valid version of IEC60601-1. If in doubt,
consult the technical service department or your local
representative for GE.
Connecting probes
Please refer to User Manual on how to connect/disconnect a
probe.
Powering the system

Please refer to User Manual on how to power the system.

5610739-100 English Rev.10
System Setup
System Configuration

This section describes how to configure the LOGIQ V2/LOGIQ
V1.
LOGIQ V2/LOGIQ V1 configuration

For complete instructions, refer to the latest revision of the
LOGIQ V2/LOGIQ V1 Basic User Manual, Chapter 16.
Information includes Entering Location, Adjusting Date and
Time, Selecting User interface Language, Selecting Online
Manual Language, Selecting Unites of Measure.

5610739-100 English Rev.10
Overview
This section describes how to install and configure the
peripherals validated for the LOGIQ V2/LOGIQ V1.
About the operation check-out of peripherals, See ‘Peripheral
checks’ on page 4-39 for more information.
Table 3-4: LOGIQ V2/LOGIQ V1 Peripherals
Description Control Model
B/W USB Printer USB port Sony UP-D897 Printer
B/W USB Printer USB port Sony UP-D898MD Printer
Color USB Printer USB port Sony UP-D25MD Printer
Officejet 100 Printer USB port HP Officejet 100 Printer
Officejet Pro 8100 Printer USB port HP Officejet Pro 8100 Printer
1-Pedal Footswitch USB port Footswitch FSU-1000
3-Pedal Footswitch USB port MKF 2-MED GP26
USB Stick USB port Keeber USB Flash Drive 8G
USB3.0 HDD USB port WD Elements 2.5 in USB3.0 HDD 1TB
USB3.0 HDD USB port Seagate Backup Plus 2.5 in USB3.0 HDD 1TB
USB3.0 HDD USB port Seagate Expansion 2.5 in USB3.0 HDD 1TB
Wireless Adapter USB port Netgear A6210 USB Adapter
Probe Adapter Probe port 2 Probe Port Extension Adapter

5610739-100 English Rev.10
System Setup
Furnished materials
This section describes the materials furnished with the
Peripherals and with the system.
Retain the original carton and packing materials in case
transport is needed in the future.
• B/W USB Printer
Table 3-5: Materials furnished with B/W Printer
Item Description Quantity Note
1 Sony UP-D897 Printer 1
2 Sony UP-D898MD Printer 1
3 Paper Roll 1
4 USB cable 1
• Color USB Printer
Table 3-6: Materials furnished with Color USB Printer
1 Sony UP-D25MD Printer 1
2 Paper Roll 1
3 AC Power Cord (local purchase) 1
4 USB cable 1
• Digital Printer
Table 3-7: Materials furnished with B/W Printer
1 HP Officejet 100 Printer 1
2 HP Officejet Pro 8100 Printer 1
3 Paper Roll 1
4 USB cable 1

5610739-100 English Rev.10
Furnished materials (continued)

• USB Stick
Table 3-8: Materials furnished with USB Stick
1 Keeber USB Flash Drive 8G 1
2 Paper Roll 1
3 USB cable 1
• USB HDD
Table 3-9: Materials furnished with the USB HDD
1 USB HDD 1
2 USB Cable 1
• Footswitch
Table 3-10: Materials furnished with the Footswitch
1 1 Pedal Footswitch 1
2 3 Pedal Footswitch 1

5610739-100 English Rev.10
System Setup
Peripherals Installation Instructions
Sony UP-D25MD Printer Installation
Tools
No special tools needed.
Manpower
One person 5 min.
Preparations
1. Unpack the Sony UP-D25MD Printer.
Installation Procedure
1. Place the device in a suitable place.
2. Connect the USB Cable and power cable on the Printer.
3. Connect the power cord in the wall outlet, then turn on the
printer.
4. Connect USB cable to LOGIQ V2/LOGIQ V1 USB port.
Figure 3-6. Color printer Connection
5. Press Utility on the Control Panel.

5610739-100 English Rev.10
Sony UP-D25MD Printer Installation (continued)

6. Select Connectivity-> Service, add Standard Print.
Figure 3-7. Connectivity->Service
7. Highlight Standard Print in the Service list. Select the

printer from the Printer pull-down Properties menu. Type the
printer name in the Name Filed. This name is used on the
Button screen. After you select the printer from the Printer
pull-down Properties menu again, it turns white. Press
Save.
NOTE: After selecting the printer, the field turns white.
Figure 3-8. Select the Printer

5610739-100 English Rev.10
System Setup
Sony UP-D25MD Printer Installation (continued)

8. Select Button. Select the appropriate print key (Print, Store,
Print3) from the Physical Print Buttons selection. Select
the printer from MyComputer column and press >> to move
it to the Printflow View column. PressSave.
Figure 3-9. Select Button

5610739-100 English Rev.10
HP Officejet 100 Printer Installation
Tools
Manpower
One person 5 min.
Preparations
1. Unpack the HP Officejet 100 Printer.
2. Connect the USB Cable on the Printer.
3. Connect the power cord with the AC output in the wall outlet,
then turn on the printer.
Figure 3-10. HP Officejet 100 connection
5. Refer to the Connectivity configure steps of ‘Sony

UP-D25MD Printer Installation’ on page 3-22.

5610739-100 English Rev.10
System Setup
HP Officejet Pro 8100 Printer Installation
Tools
Manpower
One person 5 min.
Preparations
1. Unpack the HP Officejet Pro 8100 Printer.
Figure 3-11. HP Officejet Pro 8100 connection


5610739-100 English Rev.10
UP-D897 Printer Installation
Tools
Manpower
One person 5 min.
Preparations
1. Unpack the UP-D897 Printer.
Figure 3-12. UP-D897 connection


5610739-100 English Rev.10
System Setup
UP-D898MD Printer Installation
Tools
Manpower
One person 5 min.
Preparations
1. Unpack the UP-D898MD Printer.
Figure 3-13. UP-D898 connection


5610739-100 English Rev.10
Footswitch Installation
Tools
Manpower
One person 2 min.
Preparations
1. Unpack the Footswitch.
2. Ensure no physical damage.
1. Connect the Footswitch to the USB port on the LOGIQ V2/
LOGIQ V1 system.
Figure 3-14. Connect Footswitch to the system

5610739-100 English Rev.10
System Setup
Footswitch Installation (continued)
Configuring Footswitch
Footswitch supports these configurations: No Function, Freeze,
Next Heartcycle, Prev Heartcycle, Print1, Print2, Update, Next
Step (Scan Assistant), Previous Step (Scan Assistant), Scan
Assistant pause/Resume.
Enter Utility -> Application-> Settings to configure the
Footswitch functions.
Figure 3-15. Configuring Footswitch Functions

5610739-100 English Rev.10
USB HDD Installation
Tools
Manpower
One person 1 min.
Preparations
1. Unpack the USB HDD.
1. Connect the USB HDD to the USB port on the LOGIQ V2/
LOGIQ V1 system.
Figure 3-16. Connect HDD to the system

5610739-100 English Rev.10
System Setup
Wireless LAN Adapter Installation
Tools
Manpower
One person 1 min.
Preparations
1. Unpack the Wireless LAN Adapter.
1. Connect the Wireless LAN Adapter to the USB port on the
LOGIQ V2/LOGIQ V1 system.
Figure 3-17. Connect Wireless LAN Adapter to the system

5610739-100 English Rev.10
ECG Installation
Tools
Manpower
One person 1 min.
Preparations
1. Unpack the ECG.
1. Connect the ECG to the USB port on the LOGIQ V2/LOGIQ
V1 system.
Figure 3-18. Connect ECG to the system

5610739-100 English Rev.10
System Setup
Connectivity setup
TCP/IP Screen
1. Press Utility on the control panel and login as admin, refer
to ‘Logging on to LOGIQ V2/LOGIQ V1 as “ADM”’ on
page 4-11 .
2. Select Connectivity on the screen.
3. Select TCP/IP tab, the screen gives an overview of the
network settings for LOGIQ V2/LOGIQ V1.
Figure 3-19. TCP/IP Screen

5610739-100 English Rev.10
Connectivity setup
Changing the AE title and/or Port Number
To change AE Title and/or Port Number, edit the respective

fields.
Figure 3-20. AE Title/Port No
Network setup
For network connection setup, See ‘Network Configuration’ on
page 8-26 for more information.

5610739-100 English Rev.10
System Setup
Setup the LOGIQ V2/LOGIQ V1 for DICOM Communications

LOGIQ V2/LOGIQ V1 is configured to work with DICOM servers
in a network environment. Images are first saved on the local
image butter on the system. At the end of the examination the
images are sent to the DICOM server via a DICOM spooler and
to the local database, depending on dataflows.
To connect to the DICOM server, the following information has to
be entered in the system.
• The DICOM server IP address
• The DICOM server port number
• The DICOM server AE title (the server application's name)
Table 3-11: Utility ->Connectivity ->TCP/IP screen
1 Enter the LOGIQ V2/LOGIQ V1 computer name. This may be the same as the station
name.
2 Enter the LOGIQ V2/LOGIQ V1 IP address, subnet mask, default gateway and
network speed. For automatic assignment of IP address, subnet mask and default
gateway, select DHCP.
Note: If possible, set the LOGIQ V2/LOGIQ V1 network Speed to match that of the Network
switch. if in doubt, set it to AutoDetect. Otherwise, transfer times can be two or five times
longer, during which the LOGIQ V2/LOGIQ V1 will appear to be locked up. (If the Hard
Drive activity light on the front of the console is lit steady or blinks quickly, the LOGIQ V2/
LOGIQ V1 is most likely not hung.)

5610739-100 English Rev.10
Connectivity setup
Setup the LOGIQ V2/LOGIQ V1 for DICOM Communications

(continued)
Table 3-12: Utility ->Connectivity ->Device screen
1 Select MyComputer.
2 Assign an AE title to the LOGIQ V2/LOGIQ V1. (AE stands for Application Entity.
DICOM services use this to identify the LOGIQ V2/LOGIQ V1.) AE title is
case-sensitive. This title may contain the Computer Name from the TCP/IP page,
if desired.
Note: It is NOT recommended to use the factory default. This is not prohibited, but
more than one system with the same AE title can cause confusion.
3 Edit Port Number if needed. 104 is typical. Save your changes and reboot the
system.

5610739-100 English Rev.10
System Setup
How to get the LOGIQ V2/LOGIQ V1 to recognize another Device on

the Network
Table 3-13: Utility ->Connectivity ->Device screen
1 Select Add. The system creates a device called “NewDevice”.
2 Change the name to one of your choosing.
3 Enter the IP address of the device.
4 Save your changes and then press Ping. A “Smiley Face” indicates successful
communication between your LOGIQ V2/LOGIQ V1 and the device. A “Frown”
indicates failed communication. Check the following:
• Is the device running?
• Is it connected to the network?
• Did you enter the right IP address?

5610739-100 English Rev.10
Connectivity setup
How to Setup and Use a DICOM Image Storage Service

An Image Storage Service provides a place to store patient and
exam data from LOGIQ V2/LOGIQ V1 and corresponding
images. The Image Storage Service, or the device that hosts it,
is often called a Patient Archiving and Communication System
(PACS).
Table 3-14: Setup an Image Storage Service
1 In Utility -> Connectivity -> Service, from the Destination Device drop-down menu,
select the device on which the service resides. (This assumes you have already setup
the device in the Device tab in ‘How to Setup and Use a DICOM Image Storage Service’ on
page 3-39 .
2 From the Select Service Type to add drop-down menu, select DICOM Image Storage
and press Add.
3 Change the name of the service to one of your choosing.
4 Enter the AE Title and port Number of the service. AE Title is case-sensitive.
4 Save your changes and then press Verify. A “Smiley Face” indicates successful
communication with the service.
Note: If you get a successful Ping (Smiley Face) at the device level but not at the
service level, it is possible that the AE Title or Port Number of the service settings are
incorrect. Ensure that these are correct then re-verify. Be sure that the service type
(Store, Print, etc) is correct and supported by the device.

5610739-100 English Rev.10
System Setup
Option Setup
Software Option Installation Procedure

NOTE: Not all features described in this section may be available or
cleared for sale in all markets. Please contact with your local GE
Ultrasound representative to get the latest information.
1. Power on the system.
NOTE: Keep the power cord connection during the installation.
2. After the power-up sequence is complete, press Utility on
the control panel, and then select Admin.
WARNING For software Option Installation, the operator must login as

Administrator.
3. In System Admin tab, enter New Option Key, and then

select Add.
Figure 3-21. New Option Key

5610739-100 English Rev.10
Option Setup
Software Option Installation Procedure (continued)

4. Select OK to restart the system.
Figure 3-22. Dialog Window
NOTE: There is no need to restart the system after each

installation, if several option keys are installed at one time.
Select Cancel for the first several times, and select OK after
the last installation to activate all the changes.
5. After the system is powered on, check the option status.
The option status explanation:
• Valid: This option is enabled in the system.
6. Exit and check the function of the option installed.

5610739-100 English Rev.10
System Setup
Paperwork after setup
NOTE: During and after setup, the documentation (i.e. CDs with
documentation, User Manuals, Installation Manuals, etc.) for the
LOGIQ V2/LOGIQ V1 and the peripherals must be kept as part
of the original Ultrasound system documentation. This ensures
that all relevant safety and user information is available during
the operation and service of the complete Ultrasound system.
Contents in this Section

• ‘User’s Manual(s)’ on page 3-42
• ‘Product Locator Installation Card’ on page 3-42
User’s Manual(s)
User Check that the correct User Manual(s) for the system and
software revision, is included with the installation. Specific
language versions of the User Manual may also be available.
Check with your GE Sales Representative for availability.
Product Locator Installation Card

NOTE: The Product Locator Installation Card shown may not be the
same as the provided Product Locator card.
Figure 3-23. Product Locator Installation Card (Example)

5610739-100 English Rev.10
Chapter 4
General Procedures and

Functional Checks
This chapter provides procedures for quickly checking

major functions of the LOGIQ V2/LOGIQ V1 and
diagnostics instructions using the built-in service
software.

5610739-100 English Rev.10
General Procedures and Functional Checks
Overview
Purpose of this chapter

This chapter provides procedures for quickly checking major
functions of the scanner and diagnostics instructions using the
built-in service software.

• ‘General procedures’ on page 4-3
• ‘Functional checks’ on page 4-24
• ‘Power supply test & adjustments’ on page 4-40
Special Equipment required

To perform these tests, you'll need any of the sector, linear, or
convex probes. (Normally you should check all the probes used
on the system).

5610739-100 English Rev.10
General procedures
General procedures
CAUTION Ultrasound system requires all covers.

Operate this Ultrasound system only when all board covers and
frame panels are securely in place. The covers are required for
safe operation, good Ultrasound system performance and
cooling purposes.

5610739-100 English Rev.10
Overview
Some procedures are used more often than other. The intention
with this section is to keep the most used procedures in one
place.
• ‘Power ON/Boot Up’ on page 4-5

• ‘Power off’ on page 4-9
• ‘Logging on to LOGIQ V2/LOGIQ V1 as “ADM”’ on
page 4-11
• ‘Service Key (Dongle, HASP)’ on page 4-12
• ‘Exit to Windows Desktop from the LOGIQ V2/LOGIQ V1
application software’ on page 4-13
• ‘Removable media’ on page 4-17
• ‘Archiving and loading presets’ on page 4-18
• ‘Data Management’ on page 4-20
• ‘Backup’ on page 4-20
• ‘Cleaning the Trackball’ on page 4-22

5610739-100 English Rev.10
General procedures
Power ON/Boot Up
Warnings
DANGER ALWAYS CONNECT THE ULTRASOUND SYSTEM TO A

FIXED POWER SOCKET WHICH HAS THE PROTECTIVE
GROUNDING CONNECTOR.
DANGER NEVER USE A THREE-TO-TWO PRONG ADAPTER; THIS

DEFEATS THE SAFETY GROUND.
DANGER ENSURE THAT THE POWER CORD AND PLUG ARE

INTACT AND THAT THE POWER PLUG IS THE PROPER
HOSPITAL-GRADE TYPE (WHERE REQUIRED).
CAUTION Ultrasound system requires all covers.

Operate this Ultrasound system only when all board covers and
frame panels are securely in place. The covers are required for
safe operation, good Ultrasound system performance and
cooling purposes.
CAUTION Use only power supply cords, cables and plugs provided by or
designated by GE.

5610739-100 English Rev.10
Connect AC (mains) Power to LOGIQ V2/LOGIQ V1
Lower the handle. Plug the AC adapter output connector into the
system DC input port (located on the system’s rear panel) with
the arrow side upward. Plug the AC adapter power cord into a
grounded, protective earth outlet.
After AC/DC is connected correctly to the scanner, the power is
applied to the scanner. When the Power On/Off key is pressed
once, the System starts.
Figure 4-1. Connect AC Adapter

5610739-100 English Rev.10
General procedures
Switch ON the AC Power to LOGIQ V2/LOGIQ V1
Press once on the On/Off key on the Operator Panel to boot the
unit.
During a normal boot, you may observe that:
a. The unit’s ventilation fan starts on full speed, but slows
down after a few seconds (listen to the fan sound).
b. Power is distributed to the peripherals, Operator Panel
(Console), Monitor, Front End Processor and Back End
Processor.
c. Back End Processor and rest of scanner starts with the
sequence listed in the next steps:
d. Back End Processor is turned ON and starts to load the
software.
e. The Start Screen is displayed on the monitor.
f. A start-up bar indicating the time used for software
loading, is displayed on the monitor.
g. The software initiates and sets up the Front End
electronics and the rest of the instrument.
h. The backlight in the keyboard is lit.
i. As soon as the software has been loaded, either a 2D
screen is displayed on the screen, indicating that a
probe has been connected, or a No Mode screen is
displayed, indicating that no probe has been connected.
NOTE: Total time used for start-up is typical one and a half minutes
or less. If starting after a power loss or a lock-up, the
start-up time may be up to four minutes.

5610739-100 English Rev.10
Check System Date and Time
A warning message “Please check the system date and time are
correct” appears on the screen when the system is powered on.
This warning message appears for the possible reasons:
• The system is not boot up for over 14 days.
• The system time has been changed by 24 hours earlier than
the current system time of last boot-up.
This warning message is to remind the user to check the system
date in case the system date and time is incorrect.
Figure 4-2. Check system date and time message
Move the cursor to OK and press Cursor key on the control

panel to select OK. The system enters scanning mode.
Check the system date and time. If it is incorrect, follow below
steps to reset the system date and time.
1. Enter Utility -> System -> General -> Date/Time.
2. Reset the system date and time.
3. Select Apply and then select OK.
4. Select Save.

5610739-100 English Rev.10
General procedures
Power off
When you switch off the unit, the system performs an automatic
shutdown sequence.
The SYSTEM - EXIT menu, used when switching off the unit,
gives you these choices:
Figure 4-3. System Exit Window
• Logoff
Use this button to log off the current user.
The system remains ON and ready for a new user to log on.
If the Logoff button is dimmed, it indicates that no user is
logged on to the unit at the moment.
• Shutdown
Use this button to shut down the system. The entire system
will shut down. It is recommended to perform a full shutdown
at least once a week.
If the Shutdown button is dimmed, use the key-combination
<Ctrl+Alt+Delete> to shut down the unit.
NOTE: To enable the key-combination <Ctrl+Alt+Delete>, the
dongle should be connected to the system.

5610739-100 English Rev.10
Power off (continued)

• Exit
(Only available when logged in as GE Service with Service
Dongle)
Select this button when you want to exit to Windows
Desktop.
• Cancel
Use this button to exit from the System-Exit menu and
return to the previous operation.
System shutdown
Disconnect the Mains Power Cable is necessary. For example:

Relocating the scanner.
CAUTION DO NOT unplug and/or transport the unit until after the power
off sequence has been completed. Failure to do so may result
in corrupted patient files.

5610739-100 English Rev.10
General procedures
Logging on to LOGIQ V2/LOGIQ V1 as “ADM”

Select Utility -> Admin -> System Admin.
It will bring up the Operator Login dialog where you must log
on.
Figure 4-4. Operator Login Window
1. Operator: Select the operator.

2. Password: Enter Operator’s password (optional).
3. Select the type of Login or Cancel.
• OK: Standard login.
• Cancel: Cancel login.
As default, two users are defined, USR and ADM.
• USR
If you log on as USR, you will have access to do set-up tasks
that a user may need to do during daily use.
• ADM
If you log on as ADM, you will have access to do general set-up,
service adjustments, adjust network and connectivity settings.
Select the name ADM, the password and select Login.
It is possible for the administrator (ADM) to establish new users
and set unique passwords for each user, including a new
password for ADM. If the login as ADM fails, contact the
responsible person in the hospital to get access.

5610739-100 English Rev.10
Service Key (Dongle, HASP)

A Service Dongle and a proprietary GE Service password are
necessary for use by GE Service when performing proprietary
level diagnostics like accessing the desktop on the BEP. The
password used with the GE service dongle changes at specific
intervals.

5610739-100 English Rev.10
General procedures

software
Follow these steps if you want to exit to the Windows Desktop
when the application software is running. The Service Dongle
must be plugged in.
1. On the alphanumeric keyboard, press Ctrl+Alt+Delete and
then select Task Manager.
Figure 4-5. Windows Security (For R1.0.x)
Figure 4-6. Windows Security (For R1.1.x)

5610739-100 English Rev.10

software (continued)
2. Select EchoLoader.exe in the Process list, then select End
Process.
Figure 4-7. Maintenance Access
3. Select Yes to continue.
Figure 4-8. Task Warning
4. Leave the Username field empty, type the current GE

Service Password in the Password field.

5610739-100 English Rev.10
General procedures

Figure 4-9. Maintenance Access
NOTE: READ THIS NOTE BEFORE YOU CONTINUE: After you

have selected OK, the Start Application dialog will be
displayed on screen. Be ready to select MAINTENANCE...
before the Time Bar is “full”, or the application software will
be started. A description on how to recover, if you fail to
select MAINTENANCE... is included, but you will spend
some extra time doing it.

5610739-100 English Rev.10

5. Select MAINTENANCE... to enter maintenance mode. This
will bring up the Maintenance dialog.
Figure 4-10. System halted
6. In the Maintenance window, select Exit to Windows. This

will display the Windows Desktop on the screen.
Figure 4-11. Maintenance dialog
NOTE: If you need to restart, ensure that you do a complete power

down (Shut Down). This is required to power up the Front End
Processor.

5610739-100 English Rev.10
General procedures
Removable media
Refer to the latest revision of the User Manual to perform the
following tasks:
• Using Removable Media
• Labeling Removable Media
• Formatting Removable Media
• Verifying Removable Media

5610739-100 English Rev.10
Archiving and loading presets

NOTE: Always save presets before any software reload. This ensures
the presets loaded after the software reload are as up–to–date
as possible.
All user presets except changes to Summary, Anatomy, and
Biometry pages, can be saved on an DVD-R disk (or USB
memory device) for reloading on the system.
NOTE: Presets should NOT be saved on the same USB memory device
(or DVD-R disk) as images. The Archive Menu lists the images
but does NOT list the presets stored on a USB memory device
(or DVD-R disk, SD Card).
Archiving Presets to a USB memory device (or DVD-R Disk, SD Card)
1. Connect the USB memory device to the system’s USB port,

or insert an empty (blank) DVD-R disk into the DVD-RW.
2. Enter Utility -> System -> Backup/Restore. The Backup/
Restore sheet will be shown on the LCD display.
Figure 4-12. Backup Sheet

5610739-100 English Rev.10
General procedures
Archiving Presets to a USB memory device (or DVD-R Disk, SD Card)

(continued)
3. Select the item to Backup.

4. Enter backup destination or browse through the disk to
locate the destination.
5. Select Backup. The backup status for each item is displayed
on the Result column.
Loading Presets from a USB memory device (or DVD-R)
1. Connect the USB memory device or DVD-R with the

archived Presets to the system.
2. Enter Utility -> System -> Backup/Restore. The Backup/
Restore sheet will be shown on the LCD display. See
Figure 4-12 on page 4-18.
3. Select the items needed to be restored.
4. Select Restore. The system performs the restore and
restarts.

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Data Management
Refer to the latest revision of the LOGIQ V2/LOGIQ V1 User
Manual to perform the following tasks:
• Configuring the Disk Management Function
• Setting the Disk Management Schedule
• Configuring Data Management Settings
• Configuringestination Device Setting
• Running the Disk Management Function
• Starting Disk Management Manually
Backup
For more information, refer to the latest revision of the LOGIQ
V2/LOGIQ V1 User Manual.
Restore the factory defaults

For instructions, please see “Data Backup and Restore” in the
User Manual/User Guide.
Installation and Setup Procedure for Peripherals

Please refer to ‘Peripherals Installation Instructions’ on
page 3-22.

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General procedures
Where are the User Manuals and the Service Manual?

Online versions of the User Manuals are available via the help
function.
Both the User Manuals and the Service Manual are delivered as
PDF files on a CD-ROM. Paper copies may be ordered from
GE.
How to display or print the PDF files from the Manual CD?
1. Insert the CD-R disk (CD-ROM) into the CD-drive on a PC
or Laptop with Adobe Acrobat Reader.
CAUTION Do not try to use the LOGIQ V2/LOGIQ V1 to read these files, it
will not work!
2. Follow the instructions on the screen to display the manual

of choice.
3. Before printing the complete manual, or pages from the
manual, select File > Page Setup.
4. Select the paper size and choose Portrait.
5. Select File > Print to start printing. In the pop up window,
you may choose which pages to print and the number of
copies you want to print (usually 1 copy).

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Cleaning the Trackball

equipment.
Manpower
One person, 5 minutes,
Tools
• Antistatic brush and/or antistatic vacuum cleaner
Preparations
To get access to the trackball for cleaning, you must perform the
following steps:
1. Power down the system.
2. Disconnect the mains power cable from the wall outlet.
Follow these links if you need more information: See ‘Power off’
on page 4-9 for more information.

5610739-100 English Rev.10
General procedures
Clean the Trackball
Dust is often building up behind the ball, so it interferes with the

ball rotation and for optical trackballs the light used for sensing.
To get access for cleaning, you need to remove the ball.
The ball is held in position by the Dust Gasket.
1. Power off the system.
2. Rotate the dust gasket counterclockwise until it can be
removed from the keyboard.
Figure 4-13. Remove the retainer
3. Separate the trackball and the gasket. Wipe off any oil or
dust from the trackball, gasket and the trackball housing
using a cleaner or cotton swab.
4. Assemble the trackball and gasket, then put it into the
housing and rotate it clockwise until its notches are set in
the position.
CAUTION When cleaning, make sure not to spill or spray any liquid into
the trackball housing (keyboard or system).
Test the Trackball
Power up the system and test that the trackball now works as
intended.

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Functional checks
Overview
In this section, the functional checks for LOGIQ V2/LOGIQ V1
are described. Functional checks are used to verify that the
product works as intended. Functional checks may also be used
during troubleshooting.
Contents in this Section
Preparation
Turn on power to LOGIQ V2/LOGIQ V1. For detailed
description, See ‘Power ON/Boot Up’ on page 4-5 for more
information.

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Functional checks
Basic Controls
Operator Panel
Figure 4-14. Control Panel Map
1. Power On/Off Switch 11. Worksheet key 21. Measure key

2. Primary menu Key 12. End Exam key 22. Body Pattern key
3. Next Key 13. Archive key 23. M/D Cursor key
4. TGC 14. Gain/AO keys 24. Scan Area key
5. AN Keyboard 15. Scan Coach keys 25. Set/B Pause key
6. User Defined keys 16. Mode keys 26. Trackball
7. Report key 17. Cursor key 27. Depth/Zoom/Ellipse key
8. Utility key 18. Clear key 28. Left/Right key
9. Patient key 19. Comment key 29. Freeze key
10. Preset Key 20. Active key 30. Print key
31. Store key

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Performance Tests
Test Phantoms
The use of test phantoms is only recommended if required by

your facility's (customer’s) QA program.

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Functional checks
B mode Checks
Introduction
The B Mode is the system’s default mode.
B Mode Screen Example
Preparations
• Connect one of the probes.
• Turn ON the scanner.
The B Mode is displayed (default mode).
Adjust the B mode controls

Press B on the Operator Panel to access B mode.
These Image Controls are used to optimize the B Mode picture.
Verify that all the listed controls are working as intended:
• Use Gain and TGC controls to optimize the overall image
together with the Power control.
• Use Depth to adjust the range to be imaged.
• Use Focus to center the focal point(s) around the region of
interest.
• Use Frequency (move to higher frequencies) or Frame rate
(move to lower frame rate) to increase resolution in image.
• Use Frequency (move to lower frequency) to increase
penetration.
• Use the Reject control to reduce noise in the image.
• Use the DDP control to optimize imaging in the blood flow
regions and make a cleaner, less noisy image.
• Use UD Clarity (Cardiac) or UD Sp. Red. (non-cardiac) to
reduce image speckle. Extra care must be taken to select
the optimal Speckle reduction level, as too much filtering of
speckle can mask or obscure desired image detail.
• Use Adaptive reject (Cardiac) to reduce near field haze
and blood pol artifact without diluting tissue appearance of
moving structures.

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M Mode Checks
M-Mode Screen Example
Preparations
• Connect one of the probes to the scanner’s left-most probe

connector.
The 2D Mode window is displayed (default mode).
• Press M on the Operator panel to bring up an M-Mode
picture on the screen.
Use the trackball to position the cursor over the required
area of the image.
Adjust the M Mode controls
These Image Controls are used to optimize the M mode picture.

Verify that all the listed controls are working as intended:
• Adjust Horizontal sweep to optimize the display resolution.
Adjust Gain and TGC controls to adjust the range to be
imaged.
Use the Frequency (move to higher frequencies) or the
Frame rate control (move to lower frame rate) to increase
resolution in image.
Use the Frequency (move to lower frequency) to increase
penetration.
Adjust Focus to move the focal point(s) around the region of
interest in the M-Mode display.
Adjust Dynamic range to optimize the useful range of
incoming echoes to the available grey scale.
Adjust Compress and Edge Enhance to further optimize
the display.
Adjust Reject to reduce noise while taking care not to
eliminate significant low-level diagnostic information.

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Functional checks
Color Mode Checks
Introduction
Color Flow screens are 2D or M Mode screens with colors

representing blood or tissue movement.
Color Flow may be selected both from 2D mode or from M mode
or a combination of these.
Preparations
• Connect one of the probes to the scanner’s left-most probe

connector.
The B Mode window is displayed (default mode).
Select Color Mode
1. From an optimized B Mode image, press CF.

2. Use the trackball to position the ROI frame over the area to
be examined.
3. Press Scan Area. The instruction Size should be
highlighted in the trackball status bar. Use the trackball to
adjust the dimension of the ROI.

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Adjust the Color Mode controls

• Adjust the Active mode gain to set the gain in the color flow
area.
Adjust Scale to the highest setting that provides adequate
flow detection.
NOTE: The scale value may affect FPS, Low Velocity Reject, and
Sample Volume.
Adjust Low Velocity Reject to remove low velocity blood
flow and tissue movement that reduces image quality.
Adjust Variance to detect flow disturbances.
Adjust Sample volume (SV) to a low setting for better flow
resolution, or a higher setting to more easily locate disturbed
flows.
Adjust Frequency to optimize the color flow display. Higher
settings improve resolution. Lower settings improve depth
penetration and sensitivity. This does not affect the
frequency used for 2D and M-Mode.
NOTE: Frequency setting may affect FPS, SV and Low Velocity
Reject.
Adjust Power to obtain an acceptable image using the
lowest setting possible.
NOTE: The Power setting affects all other operating modes.
Adjust the following settings to further optimize display of the
image:
• Use Invert to reverse the color assignments in the color flow
area of the display.
Use Tissue priority to emphasize either the color flow
overlay, or the underlying grey scale tissue detail.
Use Baseline to emphasize flow either toward or away from
the probe.
Use Radial and Lateral Averaging to reduce noise in the
color flow area. Radial and Lateral Averaging smooths the
image by averaging collected data along the same
horizontal line. An increase of the lateral averaging will
reduce noise, but this will also reduce the lateral resolution.

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Functional checks
Select Color M Mode

1. Select M Mode.
2. Use the trackball to position the ROI frame over the area to
be examined.
3. Press Select. The instruction Size should be highlighted in
the trackball status bar. Use the trackball to adjust the
dimension of the ROI.

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Adjust the Color M Mode controls
• Adjust the Active mode gain to set the gain in the color flow
area.
Adjust Scale to the highest setting that provides adequate
flow detection.
NOTE: The scale value may affect FPS, Low Velocity Reject, and
Sample Volume.
Adjust Low Velocity Reject to remove low velocity blood
flow and tissue movement that reduces image quality.
Adjust Variance to detect flow disturbances.
Adjust Sample volume (SV) to a low setting for better flow
resolution, or a higher setting to more easily locate disturbed
flows
Adjust Frequency to optimize the color flow display. Higher
settings improve resolution. Lower settings improve depth
penetration and sensitivity. This does not affect the
frequency used for 2D and M-Mode.
NOTE: NOTE: Frequency setting may affect FPS, SV and Low
Velocity Reject.
Adjust Power to obtain an acceptable image using the
lowest setting possible.
NOTE: The Power setting affects all other operating modes.
Adjust the following settings to further optimize display of the
image:
• Use Invert to reverse the color assignments in the color flow
area of the display.
Use Tissue priority to emphasize either the color flow
overlay, or the underlying grey scale tissue detail.
Use Baseline to emphasize flow either toward or away from
the probe.
Use Radial and Lateral Averaging to reduce noise in the
color flow area. Radial and Lateral Averaging smooths the
image by averaging collected data along the same
horizontal line. An increase of the lateral averaging will
reduce noise, but this will also reduce the lateral resolution.

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Functional checks
PW Doppler Mode Checks
Introduction
PW Doppler are used to measure velocity (most often in blood).

Doppler mode can be done with a special pencil probe or with
an ordinary probe. By using an ordinary probe, you can first
bring up a 2D picture for navigation purpose and then add PW
Doppler.
Preparations
• Connect one of the probes to the scanner.

• If needed, adjust the Display’s Brightness and Contrast
setting.
Press PW to start Pulsed Wave Doppler (PW).
Use the trackball to select the Area of Interest (Sample
Volume) in PW.

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Adjust the PW Doppler Mode controls

Adjust the Active mode gain to set the gain in the spectral
Doppler area.
• Adjust Low velocity reject to reduce unwanted low velocity
blood flow and tissue movement.
In PW mode, adjust Sample volume to low setting for better
resolution, or higher setting to more easily locate the
disturbed flows.
Adjust the Compress setting to balance the effect of
stronger and weaker echoes and obtain the desired intensity
display.
Adjust Frequency to optimize flow display. Higher setting
will improve resolution and the lower setting will increase the
depth penetration.
Adjust Frame rate to a higher setting to improve motion
detection, or to a lower setting to improve resolution.
NOTE: Frequency and Frame rate settings may affect the Low
Velocity Reject.
NOTE: The Doppler Power setting affects only Doppler operating
modes.
Adjust the following settings to further optimize the display
of the image.
Use the Horizontal sweep to optimize the sweep speed.
To view signal detail, adjust Scale to enlarge the vertical
spectral Doppler trace.
Use Invert to reverse the vertical component of the spectral
Doppler area of the display.
Use Angle correction to steer the ultrasound beam to the
blood flow to be measured.

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Functional checks
Tissue Velocity Imaging (TVI) Checks
Introduction
TVI calculates and color codes the velocities in tissue. The

tissue velocity information is acquired by sampling of tissue
Doppler velocity values at discrete points. The information is
stored in a combined format with grey scale imaging during one
or several cardiac cycles with high temporal resolution.
Preparations
• Connect one of the probes, to the scanner’s left-most probe

connector.
• If needed, adjust the Display’s Brightness and Contrast
setting.
Press TVI.
Use the trackball (assigned function: Pos) to position the
ROI frame over the area to be examined.
Press Select. The instruction Size should be highlighted in
the trackball status bar.
NOTE: If the trackball control pointer is selected, press trackball to
be able to select between Position and Size controls.
Use the trackball to adjust the dimension of the ROI.

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Adjust the TVI Controls

• To reduce quantification noise (variance), the Nyquist limit
should be as low as possible, without creating aliasing. To
reduce the Nyquist limit: Reduce the Scale value.
NOTE: The Scale value also affects the frame rate. There is a trade
off between the frame rate and quantification noise.
TVI provides velocity information only in the beam direction.
The apical view typically provides the best window since the
beams are then approximately aligned to the longitudinal
direction of the myocardium (except near the apex). To
obtain radial or circumferential tissue velocities, a
parasternal view must be used. However, from this window
the beam cannot be aligned to the muscle for all the parts of
the ventricle.
NOTE: PW will be optimized for Tissue Velocities when activated
from inside TVI.
Basic Measurements
NOTE: The following instructions assume that you first scan the patient
and then press Freeze.
Check Distance and Tissue Depth Measurement
1. Press Measure once to display an active caliper.

2. Move the trackball to position the active caliper at the start
point (distance) or the most anterior point (tissue depth).
3. Press Set to fix the start point.
4. The system fixed the first caliper and displays a second
active caliper.
5. Move the trackball to position the second active caliper at
the end point (distance) or the most posterior point (tissue
depth).
6. Press Set to complete the measurement. The system
displays the distance or tissue depth value in the
measurement results window.
NOTE: To toggle between active calipers, rotate Cursor Select button.

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Functional checks
Probe/Connectors Check
NOTE: Probes can be connected at any time, whether the unit is ON or
OFF.
Connecting a Probe
1. Place the probe’s carrying case on a stable surface and

open the case.
2. Carefully remove the probe and unwrap the probe cable.
3. Put the porbe in the probe holder.
CAUTION DO NOT allow the probe head to hang free. Impact to the
probe head could result in irreparable damage.
4. Align the connector with the probe port and carefully push
into place.
5. Lock the probe latch upward.
6. Carefully position the probe cord so it is free to move, but
not resting on the floor.
Table 4-1: Probe and Connectors Checks
Step Task Expected Results
1 Select the appropriate connected probe from the The probe activates in the currently-selected
probe indicators on the Touch Panel. operating mode. The probe’s default
settings for the mode and selected exam are
used automatically.
2 Launch the application. To change application The selected application starts.

without changing the current probe, press Model on
the Touch Panel.
3 Verify there’s no EMI/RFI or artifacts specific to the No EMI/RFI or artifacts.

probe.
4 Test the probe in each active connector slot. It will display pictorial data each time.
5 Do a leakage test on the probe, See ‘Electrical It passes the test.

safety tests’ on page 10-20 for more information.
6 Repeat this procedure for all available probes.

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Cineloop Check
Introduction
A cineloop is a sequence of images recorded over a certain time

frame. When using ECG the time frame can be adjusted to
cover one or more heart cycles. When frozen, the System
automatically displays the cineloop boundary markers on either
side of the last detected heart cycle.
Preparation
• Connect one of the probes to the scanner.
• See ‘Probe/Connectors Check’ on page 4-37 for info about
connecting the probes
For available probes, see ‘Probe and Accessories’ on
page 9-9:
• Turn ON the scanner. The 2D Mode is displayed (default
mode).
Adjust the Cineloop controls

• Press Freeze.
The left and right markers are displayed on either side of the
last detected heart cycle on the ECG trace.
• Press Freeze.
The selected heart beat is played back.
• Press Freeze to freeze the cineloop.
Use the trackball to scroll through the acquisition and find
the sequence of interest.
• Adjust Cycle select to move from heart beat to heart beat
and select the heart cycle of interest.
Adjust Num cycles to increase or decrease the number of
heart beats to be played back.
Adjust Left marker and Right marker to trim or expand the
cineloop boundaries.

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Functional checks
Back End Processor checks

• If all the previous tests have been passed successfully, the
Back End Processor is most likely OK.
If the system seems to be operating erratically, please refer
to ‘Diagnostics/Troubleshooting’ on page 8-1.
Operator Panel Test

• The Operator Panel is tested when the LOGIQ V2/LOGIQ
V1 is powered up as part of the start-up scripts, run at every
start-up.
For more info, please refer to ‘Diagnostics/Troubleshooting’
on page 8-1.
Peripheral checks
Printer checks
The internal printer is controlled from the Print and Store keys
on the LOGIQ V2/LOGIQ V1’s Operator Panel.
The factory default is:
• Print for the standard printer
Store for the screen capture to clipboard
Turn OFF Power to LOGIQ V2/LOGIQ V1

See ‘Power off’ on page 4-9 for more information.

5610739-100 English Rev.10
Power supply test & adjustments
Power Supply Test Procedure

There is no need to do any special tests on the Power Supplies
if there don’t seems to be a problem that may be related to the
Power Supply.
Power Supply Adjustment

There are no adjustments on the power supply. The DC Power
is self-regulated. If a voltage is outside the specified range, it
means that something is wrong, either with the power supply
itself or with a unit connected to that specific power outlet. When
an error occur, the power will be turned off immediately.

5610739-100 English Rev.10
Complete these checks before returning the scanner to

customer for use:
Software Configuration Checks

Table 4-2: Software Configuration Checks
Step Task to do Notes
1 Verify Date and Time is correct.
2 Verify that Location (Hospital Name) is correct.
3 Verify Language settings are correct.
4 Verify assignment of Print Keys.
5 Verify all of the customer’s options are set up Demo Option strings turn on
correctly.

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Site Log
Table 4-3: Site Log
DATE SRVICE PERSON PROBLEM COMMENTS

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Chapter 5
Components and Functions

(Theory)
This chapter explains LOGIQ V2/LOGIQ V1’s system

concepts, component arrangement, and subsystem
functions.
It also describes the power distribution and the

Common Service Desktop interface.

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Components and Functions (Theory)
Overview

• ‘Block Diagram and Theory’ on page 5-3
• ‘Power Diagram’ on page 5-5
• ‘Common Service Platform’ on page 5-6

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General Information
LOGIQ V2/LOGIQ V1 is an ultrasound imaging scanner.
The system can be used for:
• 2D Gray Scale
• 2D Color Flow imaging
• M-Mode Gray Scale imaging
• Color M-Mode
• Doppler
• Different combinations of the above
Signal flow from the Probe Connector Panel to the Front End, to
the Mid Processors and Back End Processor and finally to the
LCD and peripherals.
System configuration is stored on a hard disk drive and all
necessary software is loaded from the hard disk drive on power
up.
Top Console
The Top Console includes a Standby/On switch, a keyboard,
different controls for manipulating the picture quality, controls for
use in Measure & Analyze (M&A), and loudspeakers for stereo
sound output (used during Doppler scanning).

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Block Diagram
System Diagram
Figure 5-1. LOGIQ V2/LOGIQ V1 System Block Diagram
Introduction
AC-DC adapter provides DC power input to WDC PWA.
WDC PWA is main power supply for the system, it provides multi
powers to MST PWA and IO PWA.
MST provides the main control function, 64 channels
transmitting/receiving and related signal processing, and
connects to CWD board.
IO board receives MISC signals from MST board and make
necessary processing, it provides multi-user interface (such as
HDMI, LAN, USB, S-Video etc.).
PFPC board shall transfer 64 channels to 128 channels for RS
type probe.
KBD Assy provides multi function keyboard.
2PP adapter shall expand the RS probe port quantity to two.

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Power Diagram
Power Diagram
Overview
The AC Power assy’s main tasks are to isolate and output to the
DC/DC unit which is inside the system console. The input of AC
power pack will be the AC outlet and it’s universal, the range is
AC 100V-240V, 50-60Hz. And no main power switch located on
this power pack.
AC Power
LOGIQ V2/LOGIQ V1 Power supply is an ACDC adapter which
use 100V-240V (50-60Hz) as input and DC 19V (7.9A) as
output.
Figure 5-2. ACDC Adapter

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Common Service Platform
Introduction
The Service Platform contains a set of software modules that
are common to all PC backend ultrasound and cardiology
systems. The Common Service Platform will increase service
productivity and reduce training and service costs.

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Chapter 6
Service Adjustments
This chapter describes how to test and make

adjustments to the LOGIQ V2/LOGIQ V1. You can use
these to test the system for errors.

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Service Adjustments
Overview

• ‘LCD Monitor adjustments’ on page 6-3

5610739-100 English Rev.10

This section describes how to test and adjust the scanner.
These tests are optional. You may use them to check the
system for errors.
Monitor Adjustments
To adjust the brightness and volume:
1. On the alphanumeric keyboard,
• adjust brightness with Ctrl +Home/End keys;
• adjust volume with Ctrl +PgUp/PgDn keys.
Figure 6-1. Monitor Adjustment

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Service Adjustments
Software Reload
Confirm Backups for Patient Data and Presets

• The system can format C Disk (system data disk )and
reinstall the system automatically. Although remote software
does not delete any presets or settings on the system since
it reloads the C:\partition only and application, it is
recommended to follow these steps:
• Contact the customer to allow enough lead time to back up
the system. Be sure no images are on the clipboard or in
opened exams.
• Be sure that the DICOM spooler is empty.
• Review the troubleshooting section to collect information for
future analysis (if you are troubleshooting loss of image or
patient data.)
• Be sure all USB printers and the footswitch are connected
and powered on. These USB devices will be automatically
installed during the base image load process.
• Remove all USB Hard Disk Drives and Flash Drives. Failure
to do so may result in a failure of the software reload
process and damage to the data on the USB device.
• Be sure the Customer has saved all Presets, both User
Defined and Service. This is precautionary in case the
presets need to be restored manually.
• Note any window’s type configurations, such as regional
settings, keyboards, and localization settings.

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Software Reload
System Reload procedure

If the system running, please follow the steps below:
1. Enter Utility -> Service.
2. Select GE Service in option of User Level of GEMS Service
Home page and input correct password, press OK button.
Figure 6-2. Service Login Page

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Service Adjustments
System Reload procedure (continued)

3. Enter Utility-> Common Utilities-> Disruptive Mode,
select Yes.
Figure 6-3. Enable Disruptive Mode
4. Choose Utilities in Global Service Interface, and then select

SW Reload to invoke system reload.
Figure 6-4. Utilities Window

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Software Reload

5. Select Setup Software.
Figure 6-5. Invoke System Reload
6. Reload system setup is successful, then reboot the system

to begin software reload.

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Service Adjustments

7. The software will be loading. Wait for the software
installation to complete. Status on the screen indicates the
progress.
Figure 6-6. System Reload
WARNING Do not interrupt the software loading any time.
DO
8. When the software reload process completes, the system

will reboot automatically.

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Software Reload
Software Download
Software Download setting up

1. The user receives notification of available software updates
via the envelop icon that appears in the status bar on the
bottom of the monitor.
Figure 6-7. Envelop Icon
NOTE: To update the software, you must login with administrator

privileges

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Service Adjustments
Software download and installation
Software Updates for the unit may be available for download

and installation. When a Software Update is available, a
message icon is displayed on the system exit window.
Only users with administrator rights are allowed to download
Software Updates. You first download the software, then install
the software. It is a two-step process.
Once the software installation has begun, the system is not
usable until the software installation is done. The installation can
take up to 45 minutes to complete. While installing, DO NOT
turn off system power. For this reason, you may want to perform
the software download one evening and then install the software
the next evening.
After the software installation is complete, you will be asked to
perform a few system functional checks to determine normal
system operation.
NOTE: A software download may take more than 1 hour (and may take
several hours), depending on local network conditions. During
this time, you cannot perform any other function. Please allow
sufficient time to complete the software download and
installation.
NOTE: Please ensure network connection when downloading software.
NOTE: After you press a software download button, it may take up to
three (3) seconds for the system to respond.
NOTE: Software Updates through the GE service platform may not be
available in all countries.
You receive notification of available software updates via the
envelope icon that appears in the status bar on the bottom of the
monitor.
NOTE: To update the software, you must login with administrator
privileges.

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Software Reload
Software download and installation (continued)
1. Press the on/off button on the control panel. The Exit dialog
window with software download displays.
Figure 6-8. System - Exit Dialog Window (For R1.0.x)
• Decline: You decline the software download; the

software is not downloaded, no update will be
performed. The software download will not occur and
you will not be informed about this package again.
• Download: Starts the software download.

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Service Adjustments
2. Select Download.

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Software Reload
The download process starts. The progression of the

download process is displayed.
NOTE: The download step can be paused. While paused, you can
return to normal operation. However, once the software
installation has begun, the system is not usable until the
software installation is done. While installing, DO NOT turn
off system power.
NOTE: A typical software update of about 600 Mb may take up to
60 minutes to download, but times may vary depending on
your location and network connection.
• Pause: Pauses the software download process. If you
select Pause, you can cancel out of this dialog and
return to normal scanning or you can power off the
scanner. A paused download can be resumed by
logging in as Administrator, pressing the power switch,
and selecting Resume.
• Resume: Press Resume to continue the software
download.

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Service Adjustments
3. The following dialog is displayed when the software

download is complete. Select Install.
Figure 6-12. Software Ready To Be Installed (For R1.0.x)
Figure 6-13. Software Ready To Be Installed (For R1.1.x)
• Decline: DO NOT install the downloaded software; no

software upgrade will be performed. If you decline this
installation, you WILL NOT be offered the chance to
install this software package again. You can contact with
GE Service Engineer to perform the install at a later
time.

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Software Reload
Multiple screens appear during the software installation

process. DO NOT interrupt this process AND follow
instructions as they appear on the display.
NOTE: A typical installation may take up to 15 minutes.
4. After the installation complete, select Shutdown and then
press Power On/Off button to reboot the system.
Figure 6-14. Shutdown after Software Installation (For R1.0.x)

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Service Adjustments
5. When the system starts up after the software installation has

finished, press Power On/Off button any then select Verify.

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Software Reload
6. The new software verification checklist is displayed, this

dialog is critical. You MUST perform software verification
after downloading and installing the new software.
Figure 6-18. New Software Verification Checklist
CAUTION Perform a check for all the features listed. You MUST
ensure that the entire system functions normally as
expected.
These verification results are tracked for regulatory
purposes, sent back to GE for tracking, and approved with
your signature.

5610739-100 English Rev.10
Service Adjustments
7. As you verify that each feature works correctly, select

“Passed.” If all features work correctly and “Passed” is filled
in for all features, type your signature and press OK. The
system is now ready for use.
Figure 6-19. Features check Passed

5610739-100 English Rev.10
Software Reload
WARNING However, if any of the features DO NOT function as

expected, you need to select “Failed” for this feature. Type
your signature and press OK. Then the System-Exit
Window is displayed, select Exit and then reboot the
system, the system will return to the previous software
version.
For R1.0.x software:
For R1.1.x software:

5610739-100 English Rev.10
Service Adjustments

5610739-100 English Rev.10
Chapter 7
Replacement Procedures
This chapter describes how to remove and install, or

replace, modules and subsystems in the LOGIQ V2/
LOGIQ V1. It also includes instructions for installing and
re-installing the software.

5610739-100 English Rev.10
Overview

• ‘Warnings and important information’ on page 7-3
• ‘Disassembly/Re-assembly’ on page 7-5
• ‘Loading the software’ on page 7-13

5610739-100 English Rev.10
Warnings
WARNING 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.

equipment.
NOTE: Use an ESD compatible work space or the ESD-kit during parts
replacement.

5610739-100 English Rev.10
Warnings (continued)
WARNING The waste of electrical and electronic equipment must not be

disposed as unsorted municipal waste and must be collected
separately.
Please contact the manufacturer or other authorized disposal
company to decommission your equipment.
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.

5610739-100 English Rev.10
Warning and Caution
WARNING ONLY QUALIFIED SERVICE PERSONNEL SHOULD

REMOVE ANY COVERS OR PANELS. ELECTRICAL
HAZARDS EXISTS AT SEVERAL POINTS INSIDE.
BECOME THOROUGHLY FAMILIAR WITH ALL
HAZARDOUS VOLTAGES AND HIGH CURRENT
LEVELS TO AVOID ACCIDENTAL CONTACT
CAUTION Do not wear the ESD wrist strap when you work on live circuits
and more than 30V peak is present.

5610739-100 English Rev.10
Tools needed for servicing LOGIQ V2/LOGIQ V1

Table 7-1: Standard tools list for LOGIQ V2/LOGIQ V1
Part
No Name Part No. QTY Screw Description Screwdriver Description
1 screw 2159632 2 Screw BH M4x6 Common Phillips Screwdriver
2 screw 2159634 4 Screw BH M4x10 WHT Common Phillips Screwdriver
3 screw 2327793 135 D2 Screw SJ2836-87 Common Phillips Screwdriver

M3x8
4 screw 2373562 3 Screw M4x10 Common Phillips Screwdriver
5 screw 5138465 10 Screw FH M2.5x5(NL) Common Phillips Screwdriver
6 screw 5176890 6 Screw DIN965A M4x8 Small Phillips Screwdriver
7 screw 5244775 2 Screw GB T820-2000 Common Phillips Screwdriver

M3x8
8 screw 5342274 4 Inch SScrew #6-32UNC Common Phillips Screwdriver
9 screw 5439265 246 Screw-M4x10 Common Phillips Screwdriver
10 screw 5445720 12 GB 818-2000 M4x30 Common Phillips Screwdriver
11 screw 2337572 2 Screw FH M3x6 Common Phillips Screwdriver
12 screw 5476381 20 Bolt M8x18 with Washer 6# Inner Hexangular Set
13 screw 5476387 34 Bolt M6x15 with Washer 5# Inner Hexangular Set
14 screw 5476394 5 Bolt M8x30 6# Inner Hexangular Set
15 screw 5476438 14 Bolt M8x36 With Washer 6# Inner Hexangular Set
16 screw 5476440 17 Bolt M6x24 With Washer 5# Inner Hexangular Set
17 screw 5477579 2 Screw_DIN912 M6_20 5# Inner Hexangular Set
18 screw 5490719 4 Screw PM SW4x8 Common Phillips Screwdriver
19 screw 5491747 1 Screw Pan Head M4x4 Common Phillips Screwdriver
20 screw 5491847 2 Hand Screw M2p5x5 by hand
NOTE: Please use the correct Screwdrivers listed in Table 7-1

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Trackball Roller Cleaning

1. Rotate the retainer counterclockwise until it can be removed
from the keyboard.
Figure 7-1. Rotate the retainer
2. Seperate the trackball and the retainer. Wipe off any oil or
dust from the trackball, retainer and the trackball housing
using a cleaner or cotton swab.
3. Assemble the trackball and retainer, then put in into the
housing and rotate it clockwise until its notches are set in
position.
CAUTION When cleaning, make sure not to spill or spray any liquid into
the trackball housing (keyboard or system).

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2-Probe Holder (5727508)

Purpose: This is a description on how to remove and replace the
2-Probe Holder.
Tools
• Common Phillips screwdrivers
Preparation
• Lock the castors in order to avoid cart moving.
Needed Manpower
• 1 person, 5 minutes + travel

5610739-100 English Rev.10
2-Probe Holder (5727508) (continued)
Removal Procedure
Table 7-2: Removal Procedure for 2-Probe Holder
No. Steps Corresponding Graphic
1. Unscrew the 6 screws under the top

table.
2. Remove the probe holder from the top

of table.
2-Probe Holder (5727508)
Mounting Procedure
1. Install the new parts in the reverse order of removal.

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Paper Tray Kit (5727505)

Paper Tray Kit of V Cart.
Tools
• None
Preparation
Needed Manpower
Removal Procedure
Table 7-3: Removal Procedure for Paper Tray Kit
1. Hold the paper tray with two hands and

push it up.
2. Then remove it from the Upper Column.
Mounting Procedure

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Printer Shelf (5727506)

Printer Shelf of V Cart.
Tools
• Common Phillips screwdrivers
Preparation
Needed Manpower

5610739-100 English Rev.10
Printer Shelf (5727506) (continued)
Removal Procedure
Table 7-4: Removal Procedure for Printer Shelf
1. Remove the screw pad.
2. Unscrew the 2 screws.
3. Hold the printer shelf with two hands

and push it up. Then remove the printer
shelf from the Upper Column.
Mounting Procedure

5610739-100 English Rev.10

This section describes how to reinstall software on
LOGIQ V2/LOGIQ V1.
Customer provided prerequisite

• Formatted and labelled media for Images storage.
• Formatted and labelled media for Patient Archive and
Presets (User Defined Settings).
• Password for the user ADM.
Data Management - moving all images
CAUTION An error, or a power loss may occur.

Always backup the Patient Archive and the Presets (System
Configurations) before loading the software!
In order to complete a successful restore of the Patient
Database, as needed after a hard disk replacement, or if all the
content on the hard disk has been erased, the images must be
moved away from LOGIQ V2/LOGIQ V1 before doing backup
of the Patient Database.
Depending on the location set-up, either move the images to a
remote server or to removable media like DVD or CD discs.
• Move the images to a remote server or to removable media.

For instructions, please see “Disk management” in the User
Manual/User Guide.

5610739-100 English Rev.10
Backing up the Patient Archive and System Configurations

Always backup the Patient Archive and the Presets (System
Configurations) before loading the software!
In order to complete a successful restore of the Patient
Database, as needed after a hard disk replacement, or if all the
content on the hard disk has been erased, the images must be
moved away from LOGIQ V2/LOGIQ V1 before doing backup
of the Patient Database.
Depending on the location set-up, either move the images to a
remote server or to removable media like DVD or CD discs.
• Backup the Patient Archive and System Configurations.

For instructions, please see “Data Backup and Restore” in
the User Manual/User Guide.
Recording important settings and parameters
Overview

It is considered to be best practice to always keep a record on
paper of the settings for the LOGIQ V2/LOGIQ V1. Verify if it is
current before you start to load software!
Always keep a record of the settings for the LOGIQ V2/LOGIQ

V1 on paper. Verify if it is current before starting a software
loading! If needed, record the settings.
This subsection includes descriptions for recording data from
the following screens:

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Loading the System Software
WARNING While the software install procedure is designed to

preserved data, you should save any patient data,
images, system setups and customer presets to CD,
DVD, USB Flash Drive, or USB Hard Disk before doing a
software upgrade.
NOTE: Before loading the system software, please ensure that the
power can be continuously supplied and there is no risk of
power cut off during loading procedure.
There are two methods to load the system software:
• Load the system software with USB memory stick.
• Load the system software with SD Card.
NOTE: Before starting this procedure, remove all probes and
peripherals and remove them from the Docking Cart.
NOTE: While it is believed to be unnecessary, it would not hurt to
disconnect the system from the network and remove all
transducer.
NOTE: Please ensure AC adapter is connected during system upgrade!

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Loading the System Software with USB memory stick (For R1.0.x)
This section describes how to upgrade the software upgrade

between R1.0.x.
1. Insert the USB memory stick labeled “System & Application
Software” to the system.
2. Properly turn off the scanner by momentarily pressing the
Power On/Off Switch. In System-Exit window, select
Shutdown to shutdown the system.
NOTE: If the system will not shutdown normally, hold down the
Power On/Off Switch until the light turns off.
3. Power on the system. The system will detect the USB
memory stick automatically.
4. Select one of the options and then press Enter key to
continue. Select choice [1] to load the C disk only.
Figure 7-2. System Software load instruction

5610739-100 English Rev.10
(continued)
• To select [1], only the bootable C: partition is loaded.

This option is intended for recovery of a system that will
not boot up. It is not recommended for application
software upgrade because during upgrade process, the
data on the system would possibly be impacted.
• To select [2], wipe tool: This option is to wipe all the
patient data.
NOTE: All the patient data cannot be recovered after wipe
process.
• To select [3], Service tool. The complete disk will be
loaded. This option is recommended for application
software upgrade.
NOTE: This option is used by service engineer only. It needs
password to continue, the password is GEWuXiChina
and it is case sensitive.
NOTE: When to select [3] to load complete disk, please ensure
that any patient data on the disk has been backed up.
CAUTION If you select [3], ALL existing software and data will be erased.
If backup has not been performed, all data like Patient
Database, System Configuration and User Configurations
(Customer Presets) will be lost.
WARNING While the software install procedure is designed to

preserve data, you should select choice [1] to format disk
C only.

5610739-100 English Rev.10
(continued)
5. System USB memory stick will be loading. Wait for the

software installation to complete.
WARNING Do not interrupt the software loading at any time.
Figure 7-3. Loading Process

5610739-100 English Rev.10
(continued)
6. Select Finish when the upgrade process completes and the

system will shutdown automatically.
Figure 7-4. System upgrade complete
7. Remove the USB memory stick and then press Power On/
Off switch to power on the system.
NOTE: If you do not remove the USB memory stick, the software
system loading process repeats when the system boots up.

5610739-100 English Rev.10
(continued)
8. When the system is powered on, the following dialog

displays to indicate to input password. The password is the
same as that of service dongle.
Figure 7-5. Input password
For software R1.0.6 and above, the following dialog will

display.
There are two options for you to continue.
• If you will input a new serial number in step 9 on
page 7-21, input the password and select OK.
• If you will input the same serial number as the original in
the step 9 on page 7-21, you can select Ignore without
input of the password. Then the step 9 on page 7-21 in the
following procedure will be skipped.
Figure 7-6. Input Password

5610739-100 English Rev.10
(continued)
9. Then input the correct Serial number, select OK.

NOTE: The serial number is case sensitivity.
Figure 7-7. Input Serial Number
NOTE: The serial number can be found at the bottom of the system.
10. The serial number is reset, then the system is shut down
automatically.
Figure 7-8. Reboot the system
NOTE: Make sure the system is shut down after the serial number
is reset.

5610739-100 English Rev.10
(continued)
11. Power on the system, input the option keys if the dialog
displays.
Figure 7-9. Input Option Key

5610739-100 English Rev.10
This section describes how to upgrade the software of LOGIQ

V2/LOGIQ V1 from R1.0.x to R1.1.x and software upgrade
between R1.1.x.
NOTE: Load the disk completely to do this software upgrade from
R1.0.x to R1.1.x. When loading the complete disk, ensure that
any patient data on the disk has been backed up.
NOTE: Patient Archive, Report Archive, User Defined Configuration and
Service of R1.0.x are not compatible with R1.1.x. Do not restore
them between R1.0.x and R1.1.x.
BIOS Setting
NOTE: To upgrade the software from R1.0.x to R1.1.x, BIOS setting is
required before software upgrade procedure.
1. Power on the system. Press DEL or F2 immediately when
the BIOS information screen displays. Record the CPU
GPN number.
Figure 7-10. BIOS Revision Information
NOTE: The GPN number in the figure is for illustrational purpose

only. Refer to your actual output screen on your system for
the correct GPN number.

5610739-100 English Rev.10
Loading the System Software with USB memory stick (For R1.1.x) (continued)
2. Input the BIOS password gerural and login the BIOS.
Figure 7-11. BIOS Password
3. In the BIOS Main page, set the BIOS time to the current
time.
Figure 7-12. BIOS Time Information

5610739-100 English Rev.10
4. Check the CPU GPN number recorded on the step 1 on
page 7-23 and select AHCI for SATA Mode. There are two
setting processes to continue:
• If the GPN number is 5548771, select the AHCI via
Advanced -> SATA -> SATA Mode Selection. Press
F4 to save and exit BIOS.
Figure 7-13. SATA Mode Selection

5610739-100 English Rev.10
• If the GPN number is 5505176, select AHCI via the
Chipset -> PCH-IO Configuration -> SATA
Configuration -> SATA Mode Selection. Press F10 to
save and exit BIOS.
Figure 7-14. SATA Mode Selection
5. The system enter scanning screen automatically. Then

restart the system.

5610739-100 English Rev.10
Software Upgrade Procedure (For R1.1.x)

This section is to describe software upgrade procedure about
how to upgrade the software of LOGIQ V2/LOGIQ V1 from
R1.0.x to R1.1.x and software upgrade between R1.1.x.
NOTE: If you are going to upgrade software from R1.0.x to R1.1.x, be
sure you have completed BIOS setting before you start software
upgrade procedure.
1. Insert the Upgrade USB memory stick labeled “System &
Application Software” in the USB port of the system.
2. Properly turn off the system by momentarily pressing the
Power On/Off Switch. Then select Shutdown in the System
Exit Window.
NOTE: If the system does not shutdown normally, hold down the
Power On/Off Switch until the light turns off
3. Power on the system and it will detect the USB memory
stick automatically.
4. Select the option Load the complete disk or Load the
bootable C: partition only for software upgrade. Or select
Exit to exit the upgrade process.
Figure 7-15. Upgrade instruction

5610739-100 English Rev.10
Software Upgrade Procedure (For R1.1.x) (continued)

• Load the complete disk: the complete disk will be
loaded. This option is recommended for application
software upgrade.
WARNING If selecting Load the complete disk, all existing software and
data will be erased. If backup has not been performed, all data
like Patient Data, System Configuration and User
Configurations (Customer Presets) will be lost. Please make
sure the patient data and the configuration have been backed
up first, then upgrade the system.
NOTE: This option is used by service engineer only. It needs

password to continue. The password is GEWuXiChina
and it is case sensitive.
• Wipe tool: this option is to wipe all the patient data and
the software from the system. It is not for software
upgrade. All the patient data cannot be recovered after
wipe process.
NOTE: All the patient data cannot be recovered after wipe
process.
• Load the bootable C: partition only: this option is
intended for recovery of a system that will not boot up.
All patient data is preserved. This option is not
applicable for software upgrade from R1.0.x to R1.1.x.
NOTE: While the software installation procedure is designed to
preserve data, select choice Load the bootable C:
partition only to format disk C only. Please do not use
this option for software upgrade from R1.0.x to R1.1.x.
NOTE: C disk upgrade is not allowed between the different
version. To keep the data, the customer needs to use
export/import.

5610739-100 English Rev.10

5. If the Load the complete disk is selected.
• For R1.0.x, read the information in the Confirmation
dialogue box carefully and check the boxes before
Preset, Patient data and BIOS to confirm that the
requirements have been executed. Then input the
Installation Password: GEWuXiChina. Select Execute
to continue.
Figure 7-16. Input Password between R1.0.x

5610739-100 English Rev.10

• For R1.1.x, input the Installation Password:
GEWuXiChina. Then select Execute to continue.
Figure 7-17. Input Password between R1.1.x
If Load the bootable C: partition only is selected, the

password is not required. Select Execute to continue. The
step in the step 6 on page 7-31 will be skipped

5610739-100 English Rev.10

6. The system detects whether the SSD Firmware needs
update and pop up a message dialog. Click OK.
• If needs, the system will automatically update the SSD
Firmware and shut down afterwards. Restart the system
by pressing Power On/Off key on the control panel and
reselect Load the complete disk.
• If no, the system will automatically continue running the
software upgrade process.
Figure 7-18. Refresh SSD
7. System USB memory stick will be loading. Wait for the

software installation to complete. Status bar on the screen
indicates the progress.
WARNING Do not interrupt the software loading any time.
Figure 7-19. Loading Process

5610739-100 English Rev.10

8. The system will display upgrading result and shutdown
automatically within 30 seconds.Or click the Shutdown in
the screen to shut down the system immediately.
Figure 7-20. System upgrade complete

5610739-100 English Rev.10

If the upgrade fails, select Exit to exit the upgrade process,
then remove the USB memory stick. Insert the USB memory
stick again and repeat the upgrade process from step 2 on
page 7-27.
Figure 7-21. System upgrade fail
9. Remove USB memory stick. Then press Power On/Off

switch to power on the system.
NOTE: Remove the USB memory stick before the system restarts.
If you do not remove the USB memory stick, the software
system upgrading process repeats when the system boots
up.
NOTE: Ensure the USB memory stick is properly and securely
connected. Once the USB memory stick is accidentally
disconnected from the system during the upgrading
process, the error message will pop up: “The volume for a
file has been externally altered so that the opened file is no
longer vaild.” Insert the USB memory stick again and restart
the system to run the upgrading process from step 3 on
page 7-27.
Rewrite the System ID
If selected to load the complete disk during the software loading

process, when powering the system, the system will indicate to
rewrite the system ID. About how to rewrite the system ID,
please contact GE service for support.

5610739-100 English Rev.10
Windows License Label
After upgrading from R1.0.x to R1.1.x, Windows License Label

needs to be attached to the bottom of the system to replace the
original one.
NOTE: The Windows License Label to replace the original one is only
required for upgrade from R1.0.x to R1.1.x.
1. Take out the windows license label, pell off the yellow part of
the paster.
Figure 7-22. Windows license label
2. Make sure the backcover is clean and dry. Then align the
paster and attach it in the location illustrated by the figure.
Figure 7-23. Windows license label location
• 1: Windows License Label

5610739-100 English Rev.10
Wipe Tool
Wipe tool is intended to erase all the patient data with the
software to wipe the partitions on the system before the system
will be shipped for service.
NOTE: Wipe tool will be performed with the software USB flash drive.
Be sure your software USB flash drive is well kept.
CAUTION The system can not be boot up after wipe process.
WARNING The wipe procedure will erase all the patient data and all
existing software on the system. While the wipe procedure is
designed to preserved data, you should save any patient data,
images, system setups and customer presets to CD, DVD,
USB Flash Drive, or USB Hard Disk before doing the wipe
process.
NOTE: Before starting the wipe tool, please ensure that the power can
be continuously supplied and there is no risk of power cut off
during loading procedure.
1. Insert USB flash drive labeled “System & Application
Software” to the system.
2. Properly turn off the system by momentarily pressing the
Power/On/Off Switch. In System-Exit window, select
Shutdown to shutdown the system.
NOTE: If the system will not shut down normally, hold down the
Power On/Off Switch until the light turns off.
3. Power on the system. The system will detect the USB flash
drive automatically.

5610739-100 English Rev.10
Wipe Tool (continued)
4. For R1.0.x software, select 2. Wipe Tool and then select

Next to continue.
For R1.1.x software, select Wipe tool.
NOTE: All patient data cannot be recovered after this operation.
Contact GE service for support.
NOTE: All patient data (if any) will be destroyed! Please backup
patient data before executing erasing patient data!
Figure 7-24. Upgrade USB message (For R1.0.x)
Figure 7-25. Upgrade USB message (For R1.1.x)

5610739-100 English Rev.10
5. The system indicates all data will be erased, select Yes to

continue.
Figure 7-26. Confirmation Dialog (For R1.0.x)
Figure 7-27. Confirmation Dialog (For R1.1.x)
NOTE: All the patient data cannot be recovered after wipe process.
This wipe tool is not BAM approved as secure wipe tool.

5610739-100 English Rev.10
6. The process may take twenty minutes or more

NOTE: Do not interrupt the wipe tool process at any time until all the
partitions wiping is completed.
Figure 7-28. Wiping progress (For R1.0.x)
Figure 7-29. Wiping Process (For R1.1.x)

5610739-100 English Rev.10
7. For R1.0.x software, select OK when the process is

complete, and the system will shutdown automatically.
For R1.1.x, the system will shutdown automatically when the
wiping progress completes.
Figure 7-30. Process Complete
NOTE: As the SSD is empty after wipe process, the system cannot
boot up. The software should be loaded first after the wipe
process.
8. The wipe tool procedure has erased all patient data and all
existing software.
NOTE: After the system is returned from service, restore the patient
data, images, system setups and customer presets on your
system. Contact GE service for support.

5610739-100 English Rev.10
Software Version check out
Functional Check-out
1. Power on LOGIQ V2/LOGIQ V1 system and wait until
system booting to main screen.
2. Press Utility on the control panel.
3. Select the About button on the right.
Figure 7-31. About
4. Check whether “Software Version” is the right version for

use.
Figure 7-32. Software version

5610739-100 English Rev.10
Reload the Correct Preset Region
NOTE: After the system software loading completion, please reload the
correct preset region.
1. Reboot the system.
2. Select Utility -> General.
3. In the Location portion, select the right region in the field of
Preset Region.
Figure 7-33. Preset Region

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Option Strings Check
NOTE: After the system software loading completion, please check the
option strings to ensure that the options are activated and
working.
2. Select Utility -> Admin -> System Admin.
3. Ensure that all the installed option keys are displayed and
the status of Options are valid.
• The status “Valid” means the option keys are activated
and working.
• The status “disabled” means the option keys are not
activated and not working. Check if the option is
installed and if the serial number and option key are
correct.
Figure 7-34. Option strings

5610739-100 English Rev.10
Probe Recognition Check
NOTE: After the system software loading completion, please check to

ensure that the system can recognize the probes.
Plug in the probe. In scanning mode, the probe information is
displayed on the right top location of the screen. About the
probe specification for intended use on LOGIQ V2/LOGIQ V1.
Plug in at least one of each type of the probes and check if each
of the probes is recognized and the probe information is
displayed correctly.
Figure 7-35. Probe identification
Peripheral Device Check
Check to ensure that all the peripheral devices work properly.

For instruction of peripheral device check, See ‘Peripheral
checks’ on page 4-39 for more information.

5610739-100 English Rev.10
Reinstall DICOM Devices
Reinstall any DICOM devices used by the customers and check

to ensure these DICOM devices work properly.
The instruction about installing DICOM devices is not
incorporated in this manual. To access the instruction about
installing DICOM devices please refer to another manual Basic
User Manual. Please use the latest revision of this document.

5610739-100 English Rev.10
Chapter 8
Diagnostics/Troubleshooting
This chapter describes LOGIQ V2/LOGIQ V1how to

setup and run the tools and software that help maintain
image quality and system operation. Very basic host,
system and board levels are run whenever power is
applied. Some Service Tools may be run at the
application level.

5610739-100 English Rev.10
Overview

• ‘Gathering Trouble Data’ on page 8-3
• ‘Screen Capture’ on page 8-5
• ‘Network Configuration’ on page 8-26

5610739-100 English Rev.10
Overview
There may be a time when it would be advantageous to capture
trouble images and system data (logs) for acquisition to be sent
back to the manufacturer for analysis. There are different
options to acquire this data that would give different results
Collect Vital System Information

The following information is necessary in order to properly
analyze data or images being reported as a malfunction or being
returned to the manufacturer:
Product Name = LOGIQ V2/LOGIQ V1
From the Utility > System > About screen:
Applications Software
• Software Version
• Software Part Number
System Image Software
• Image Date
• Image Part Number

5610739-100 English Rev.10
Collect a Trouble Image with Logs

If the system should malfunction, press the Alt+D keys
simultaneously. This will collect a screen capture of the image
monitor, system presets and several log files in a date and time
stamped “.zip” file.
NOTE: This function may also be used to make a Print Screen.
This Alt+D function is available at all times.
When Alt+D is pressed, a menu box appears that allows for:
• a place to enter a description od the issue
• a checkbox to indicate a System lockup
• a choice to Export a pre-formated CD-R/DVD-R or save to
the Export directory D: drive (for remote viewing through
InSite)
Figure 8-1. Alt+D Dialog Box

5610739-100 English Rev.10
Screen Capture
Screen Capture
Button screen
There may be times when the customer or field engineer will
want to capture a presentation on the screen. This is
accomplished by first saving the image(s) to the clipboard using
a Print Key.
Check the function of the Print Key in the event that the
customer may have made some custom settings.
1. Press Utility on the Control Panel.
2. Select Connectivity from the Utilities Menu.
3. Select the Button tab on the Connectivity screen.
4. In the Button field, select Print, Store, or Print3.
If Print key is not set to Whole Screen, proceed to step 5 to
record the customer’s customized settings.
Figure 8-2. Connectivity/Button screen (For R1.0.x)

5610739-100 English Rev.10
Button screen (continued)
Figure 8-3. Connectivity/Button screen (For R1.1.x)
5. In the Destinations section, record the service that is

displayed.
6. In the Physical Print Buttons section, record the
parameters related to the service.
Setting the Store Key to Screen Capture

If the Print Key is not set to screen capture:
1. While on the Connectivity screen, with the Button tab
displayed, go to the Destinations list.
2. From the list select Copy To Dataflow. Press [>>] to add
the selection to the Printflow View section.
3. Ensure that the Physical Print Buttons section for Capture
Area is set to Whole Screen, secondary Capture and No
Image Compression.
4. The Print Key should now be set up for whole screen
capture, sending the screens to the image buffer
(clipboard).

5610739-100 English Rev.10
Screen Capture
Capturing a Screen
The following is a generic process to capture any screen from
the scanner:
1. Navigate to and display the image/screen to be captured.
2. Press Store. This will place a snapshot of the screen on the
“clipboard” displayed at the bottom of the scan image
display.
Figure 8-4. Select Image to Capture

5610739-100 English Rev.10
Capturing a Screen (continued)

3. Select and highlight the snapshot to be stored.
4. Select Save As Icon on the right side of the image screen.
Figure 8-5. Save As Icon
5. A Save dialog box will be opened. Choose the archive

location to save image on the USB Drive or CD/DVD.
Figure 8-6. Save Dialog Box
NOTE: It is better to save the image in Jpeg format. Image of this

format can be easily reviewed in the computer.

5610739-100 English Rev.10
Screen Capture
Reset the Store Key to Customer’s Functionality

If the customer had programmed the Store Key to a function
other than screen capture, restore that functionality recorded in
section ‘Setting the Store Key to Screen Capture’ on page 8-6.
Refer to Figure 8-2 on page 8-5.
1. Press Utility on the control panel.
2. Select Connectivity in the Utility menu.
3. In the Button field, select Store.
4. In the Destinations list, select the service(s) recorded in step
5, See ‘Setting the Store Key to Screen Capture’ on
page 8-6.
5. In the Physical Print Buttons section, select the parameters
related to the service recorded in step 6, see ‘Setting the
Store Key to Screen Capture’ on page 8-6.

5610739-100 English Rev.10
Common Diagnostics
Utilities
Provides two selections:
• Disruptive Mode
Allows you to enable or disable disruptive mode
troubleshooting.
• System Shutdown
Allows for system shutdown from the diagnostic menu.
Select to Restart System or Shutdown System. Also, select
to retain Disruptive Mode or Not.
After submitting to restart or shutdown a confirmation screen
gives one last chance to confirm or cancel the request.
Remote access
Remote access is a feature designed to enable OLE’s access to

customer’s desktop remotely, service engineers don’t have to be
on site to connect the physical dongle to exit to desktop, it’s
doable remotely by using this feature.
1. In the server side, select the system which the OLE would
remotely connect to, and select Connect to device.
Figure 8-7. Connect to device

5610739-100 English Rev.10
Common Diagnostics
Utilities (continued)
2. Select the CSD to Connect. Then the OLE is remotely

connected to the system.
Figure 8-8. Remotely Connect

5610739-100 English Rev.10
3. Enter Utility-> Common Utilities-> Disruptive Mode,

select Yes.
Figure 8-9. Enable Disruptive Mode
Figure 8-10. Diagnostic Application Area

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Common Diagnostics
4. If we want to see the Scan screen or have control of the unit,

we have to go to Virtual Console Observation and Start it.
Then connect using VNC.
Figure 8-11. Virtual Console Observation

5610739-100 English Rev.10
5. Select the VNC to Connect. Then the OLE is remotely

connected to the system.
Figure 8-12. Virtual Console Observation Connect

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Common Diagnostics
Service Diagnostics
MST
• GFW Swept Demodulator Test: performs a signal path test

of the swept demodulator FPGA on the GFW.
• GFW Front-End Interface Test: tests that the GFW can
access Front-End boards.
• GFW Analog Test.
• GFS Memory Access Test: tests that GFW can access to
the internal, external, external cache memory spaces.
• Front End Interface FPGA Test: reads the version of the
GFE FPGA.
• GFW Fixed Demo Test: GFW Fixed Demodulator signal
path test.
• DSP Master Clock Test: tests DSP Master Clock.

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Service Diagnostics (continued)
System
• MST Temperature Test.

• CPS Temperature Test.
• CPU Temperature Test.
• MST Voltage Test.
• CPS Voltage Test.
• FPGA Version Test.
• HV_STOP Test: tests HV-STOP mechanism and checks
each board is able to assert HV_STOP using its HV_STOP
source.
Memory
• Callisto Memory Test.

NOTE: The Callisto Memory test may fail if it is performed with other
tests at the same time.
AnalogReceive
• Noise Floor Test.

• BF Analog Rx Gain (High)
• BF Analog Rx Gain (Med)
• BF Analog Rx Gain (Low)
AnalogCW
• aCW IQ Symmetry Test

• aCW beamforming test
• aCW IQ Symmetry test
Digital Receive
• AFE IF Test
• Complex Mixer Test
• CE Decoder Test

5610739-100 English Rev.10
Common Diagnostics
Doppler Tests
• Doppler Audio Test runs the tests for Doppler.

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Service Diagnostics (continued)
PC
• Essential Test tests: PCI, PCI Express, CPU, Memory, HD

Disk and Video, CMOS, Network.
• Hard Drive Long: tests functionality of the hard drive.
• Hard Drive Short: tests functionality of the hard drive.
• Memory: tests the memory on the mother board.
• Network Adapter: Network cable must be connected.
• System board: tests the real time clock and CMOS.
• Video: tests functionality of video adapters.
PC Interactive
• AVI playback tests playing back an AVI file.

• Click “Play” to run the test. If the test is successful, you
will see a brief video clip with audio. For more
information about the test, click “More Information”.
• Click “Pass” if the test successfully reproduces the
video clip.
• Click “Fail” if the test is unable to successfully reproduce
the video clip.
• Click “Cancel” button to quit the test without recording a
test result.
• Keyboard
• Press each key on the keyboard and it will be added to
the History. Hold down a key to test the repeat of that
key. To cancel, click Cancel or press Alt-X.
• Special purpose keys like volume control or Internet
access keys may not be detected. To test the Fn key of
a notebook computer, hold down the Fn key while
pressing another key.
• Note: This diagnostic is intended to verify keyboard
keys are in good working order. It is not intended to
verify that keyboards produce desired characters.

5610739-100 English Rev.10
Common Diagnostics
PC Interactive (continued)
• Monitor
• This test is composed of various elements that verify a
monitor functions correctly. To test a monitor feature,
click the appropriate button. You can return to this dialog
by clicking the mouse button or pressing any key.
• The Combination Test helps you verify your monitor is
properly aligned, and set at the correct color depth and
resolution. Use the crosshair pattern in each corner of
the screen to visually determine if the monitor aligns
correctly. If the crosshairs appear distorted or out of
focus, a problem may exist with the monitor alignment.
Use the color spectrum array for visually verifying the
monitor color depth capacity. If the colors in the color
spectrum do no blend smoothly together, a problem
may exist with the monitor color depth. Use the
graduated horizontal and vertical alignment bars to
determine the monitor resolution capabilities. The better
you can discern individual lines as they move closer
together, the higher the resolution capabilities of the
monitor.
• The Solid Color Test helps point out malfunctioning or
dysfunctional pixels using five basic colors: red, green,
blue, black, and white. Fill the screen with an
appropriate color by clicking the associated button. If a
pixedl is malfunctioning, the pixel color will contrast with
the color of all other pixels.
• The VESA Test Patterns allow you to test the monitor for
proper luminance, geometry and focus. Click the
appropriate button to fill the screen with the associated
test pattern. You can return to this dialog by clicking the
mouse button or pressing any key.

5610739-100 English Rev.10
PC Interactive (continued)
• Trackball
• The Mouse Status Test verifies the cursor position and
mouse button state. When a mouse button is pressed,
the corresponding button on the picture will change
color. If the mouse is a wheel or scroll mouse, an arrow
will indicate the direction the wheel is being rotated.
Clicking the wheel will flash the picture of the mouse in
the Mouse Status Test area.
• The Drag and Drop Test verifies a mouse can
successfully perform drag and drop operations. Left
click the picture of the CD and drag is onto the picture of
the drive. If successful, the picture will change.
• The Double Click Test verifies a mouse can successfully
perform double-click operations. Double-click on the
picture of the monitor. If successful, the picture will
change.
• Sound generates sounds for testing the speakers.
• USB Ports lists USB Devices.

5610739-100 English Rev.10
Common Diagnostics
Assessment Utility
Probe Assessment
1. Place the probe’s carrying case on a stable surface and
open the case.
2. Carefully remove the probe and unwrap the probe cord.
3. Put the probe in the probe holder.
CAUTION DO NOT allow the probe head to hang free. Impact to the
probe head could result in irreparable damage.
4. Align the connector with the probe port and carefully push
into place.
5. Lock the probe latch upward.
6. Carefully position the probe cord so it is free to move and is
not resting on the floor.
7. Enter global service user interface as GE service.

5610739-100 English Rev.10
Assessment Utility (continued)
8. In the Diagnostic-> Service Diagnostics-> Assessment

Utility-> Probe Assessment to check the probe.
If there is no broken element and the probe is acceptable for
diagnostic, the following result window displays.
Figure 8-13. Probe Assessment Pass

5610739-100 English Rev.10
Common Diagnostics
Assessment Utility (continued)
If there are broken elements and the probe is not acceptable

for diagnostic. The assessment is fail and the failed
elements are shown in the graphic.
Figure 8-14. Probe Assessment Fail
9.
CAUTION Reboot the system after the probe assessment.

5610739-100 English Rev.10
Probe Pass/Fail Criteria

Pass
• No dead element
• Dead elements on the edge (#0, #1 or #end-1, #end)
Fail
• Max 2 weak elements on the scan line:
-3dB<elements<-2dB
• Any one of the elements in one scan line: element<-3dB

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Common Diagnostics
OP Panel Interface
Figure 8-15. OP Panel Test
Restart the system after diagnostics

Always shutdown the system and reboot after a
diagnostics session.

5610739-100 English Rev.10
Wire-LAN Network
1. Connect system with network.
2. Enter Utility-> Connectivity-> TCP/IP, in IP settings
window, check Enable DHCP, and select the proper
network speed in Network Speed.
Figure 8-16. Enable DHCP

5610739-100 English Rev.10
Wire-LAN Network (continued)

NOTE: If the user wants to set up static IP address, uncheck
Enable DHCP option, input static address in IP-address,
Subnet Mask and Default Gateway box. In Network
Speed box, choose the proper speed available.
Figure 8-17. Input Static IP
3. Select Save, and a popup window displays. Select OK to

restart the system and activate the changes.
Figure 8-18. System Restart inquiry dialog
4. The network icon at the bottom of the the screen displays as

connected.
Figure 8-19. Network Icon

5610739-100 English Rev.10
Wireless-LAN Network
NOTE: To configure the Wireless-LAN network, the operator must login

as administrator.
1. Connect the wireless adapter in the USB port.
2. Enter Utility-> Connectivity-> TCP/IP. In the section of
Wireless Network, select Configuration.
Figure 8-20. Wireless Network Settings

5610739-100 English Rev.10
Chapter 9
Renewal Parts
This chapter lists the renewal parts available for the

LOGIQ V2/LOGIQ V1.

5610739-100 English Rev.10
Renewal Parts
Overview

• List of Abbreviations
• Renewal Parts Lists

5610739-100 English Rev.10
Table 9-1: List of Abbreviations
ABBREVIATION DESCRIPTION
3D THREE DIMENSIONAL
Assy ASSEMBLY
FRU 1 Replacement part available in part hub
FRU 2 Replacement part available from the manufacturer (lead

time involved)
KBD Keyboard
LCD Liquid Crystal Display
BnV Brightness and Volume
TMST Master Board

5610739-100 English Rev.10
Renewal Parts
Renewal Parts Lists
AC Power Cord
Table 9-2: AC Power Cord
Part
Item Number Part Name Quantity FRU
001 5177123-2 AC Power Cord Europe 1 1
002 5176304-2 AC Power Cord China 1 1
003 5176773-2 AC Power Cord India 1 1
004 5177195-2 AC Power Cord Argentina 1 1
005 5176907-2 AC Power Cord UK 1 1
006 5177153-2 AC Power Cord Denmark 1 1
007 5177154-2 AC Power Cord Switzerland 1 1
008 5177187-3 AC Power Cord Australia 1 1
009 5177146-2 AC Power Cord USA 1 1
010 5400868-2 AC Power Cord Brazil 1 1
011 5176753-2 AC Power Cord Israel 1 1
012 5177126-2 AC Power Cord Japan 1 1

5610739-100 English Rev.10
Renewal Parts Lists
Operator Console Assy
Figure 9-1. Operator Console Assy
V Cart
Figure 9-2. V Cart

5610739-100 English Rev.10
Renewal Parts
V Cart
Table 9-3: V Cart
Part
Item Number Part Name Corresponding graphic Qty FRU
1400 5732311-S V Cart SVC Parts 1 1
5720204 V Cart Front Handle
5720225 V Cart Handle Clip
5720207 V Cart Cable Hook
5720221 V Cart Probe Holder

Large
5641895 V Cart Small Probe

Holder

5610739-100 English Rev.10
Renewal Parts Lists
Table 9-3: V Cart
Part
1401 5727505 V Cart Paper Tray Kit 1 1
1402 5727506 V Cart Printer Shelf 1 1
1403 5727508 V Cart Probe Holder For 1 1

2PP and Cart
1404 5725649-S V Cart Caster Kits 2 1
5725649-2S V Cart Castor Kits 2 1
1405 5730407-S V Cart Bigger 2 1
1406 5729876-S V Cart Wrench for 1 1

service

5610739-100 English Rev.10
Renewal Parts
Table 9-3: V Cart
Part
1407 5730407-2S Bigger Castor kit 1 1

including Wrench

5610739-100 English Rev.10
Renewal Parts Lists
Probe and Accessories

Table 9-4: Probes for LOGIQ V2/LOGIQ V1
Part
Item Part Name Number Center Image Frequency (MHz) Qty FRU
700 4C-RS 5451471 3.10 1 1
701 L6-12-RS 5454332 7.75 1 1
702 3Sc-RS 5433833 2.75 1 1
703 8C-RS 5434203 6.50 1 1
704 E8C-RS 5499516 6.50 1 1
705 LK760-RS 5548914 7.15 1 1

5610739-100 English Rev.10
Renewal Parts
Peripheral
Table 9-5: Peripherals for LOGIQ V2/LOGIQ V1
Item Part Number Description Qty
Footswitch
808 5338419 Footswitch FSU-1000 1
808 5338419 Footswitch MKF 2-MED USB GP26 1
USB Stick
809 5168040-4 Sandisk USB Stick 4G 1
810 5434317-3 1TB USB mobile HDD 1
Printer
811 5133106-2 Sony UPD25 Color Printer Chinese kit 1
812 5133017-2 Sony UPD25 Color Printer USA kit 1
813 5133108-2 Sony UPD25 Color Printer European kit 1
814 5133109-2 Sony UPD25 Color Printer Japanese kit 1
815 5151262 UP-D897MD B/W Printer Chinese kit 1
816 5151259 UP-D897MD B/W Printer USA kit 1
817 5151261 UP-D897MD B/W Printer European kit 1
818 5151263 UP-D897MD B/W Printer Japanese kit 1
819 5426594 HP100 Printer Chinese kit 1
820 5426595 HP100 Printer European kit 1
821 5426596 HP100 Printer Japanese kit 1
822 5426597 HP100 Printer USA kit 1
823 5151259-2 UP-D898MD B/W Printer USA kit 1
824 5151261-2 UP-D898MD B/W Printer Europe kit 1
825 5151262-2 UP-D898MD B/W Printer China kit 1
826 5151263-2 UP-D898MD B/W Printer Japan kit 1
827 5495509-2 UP-D898MD B/W Printer Brazil kit 1
System and Application USB
828 5692048-5S LOGIQ V2/LOGIQ V1 R1.0.4 System and Application 1

Software USB

Software USB

5610739-100 English Rev.10
Renewal Parts Lists
Table 9-5: Peripherals for LOGIQ V2/LOGIQ V1
Item Part Number Description Qty

Software USB

Software USB

Software USB
833 5765267-S LOGIQ V2/LOGIQ V1 R1.1.0 System and Application 1

Software USB

Software USB
ECG
835 H48952AB ECG cable kits EU 1
836 H41852LL ECG (IEC) Lead 1
837 H41852LK ECG (AHA) Lead 1
838 5146056 ECG Detachable cable AHA Type USA 1
839 5146739 ECG detachable cable IEC type EURO and ASIA 1
840 5146055 USB Cable for ECG 1
841 5129487 ECG module from Norav Isral,not applies to Muslim coutry 1
and China
842 5149641 ECG Module with Chinese label for Service part 1

5610739-100 English Rev.10
Renewal Parts
Power Cord
Table 9-6: Power Cord for LOGIQ V2/LOGIQ V1
Item Part Number Description Qty FRU
900 5177123-2 AC Power Cord Europe 1 1
901 5176304-2 AC Power Cord China 1 1
902 5176773-2 AC Power Cord India 1 1
903 5177195-2 AC Power Cord Argentina 1 1
904 5176907-2 AC Power Cord UK 1 1
905 5177153-2 AC Power Cord Denmark 1 1
906 5177154-2 AC Power Cord Switzerland 1 1
907 5177187-3 AC Power Cord Australia 1 1
908 5177146-2 AC Power Cord USA 1 1
909 5400868-2 AC Power Cord Brazil 1 1
910 5176753-2 AC Power Cord Israel 1 1
911 5177126-2 AC Power Cord Japan 1 1
V Cart With Package

Table 9-7: V Cart With Package for LOGIQ V2/LOGIQ V1
950 5720850 LOGIQ V2/LOGIQ V1 V Cart With Package 1 1

5610739-100 English Rev.10
Renewal Parts Lists
Manuals
Table 9-8: Manuals for LOGIQ V2/LOGIQ V1
1000 5610741-200 LOGIQ V2/LOGIQ V1 Manual CD 1 N
1001 5610738-100 LOGIQ V2/LOGIQ V1 Advanced Reference Manual 1 N
1002 5610739-100 LOGIQ V2/LOGIQ V1 Basic Service Manual 1 N
1003 5610735-100 LOGIQ V2/LOGIQ V1 Basic User Manual English 1 N

version
1004 5610736-100 LOGIQ V2/LOGIQ V1 User Guide English version 1 N
1005 5610736-101 LOGIQ V2/LOGIQ V1 User Guide French version 1 N
1006 5610736-106 LOGIQ V2/LOGIQ V1 User Guide Spanish version 1 N
1007 5610736-108 LOGIQ V2/LOGIQ V1 User Guide German version 1 N
1008 5610736-111 LOGIQ V2/LOGIQ V1 User Guide Italian version 1 N
1009 5610736-121 LOGIQ V2/LOGIQ V1 User Guide Dutch version 1 N
1010 5610736-127 LOGIQ V2/LOGIQ V1 User Guide Brazilian Portuguese 1 N

version
1011 5610736-129 LOGIQ V2/LOGIQ V1 User Guide Estonian version 1 N
1012 5610736-131 LOGIQ V2/LOGIQ V1 User Guide Slovenian version 1 N
1013 5610736-140 LOGIQ V2/LOGIQ V1 User Guide Japanese version 1 N
1014 5610736-141 LOGIQ V2/LOGIQ V1 User Guide Simplified Chinese 1 N

version
1015 5610736-142 LOGIQ V2/LOGIQ V1 User Guide Swedish version 1 N
1016 5610736-144 LOGIQ V2/LOGIQ V1 User Guide Korean version 1 N
1017 5610736-145 LOGIQ V2/LOGIQ V1 User Guide Russian version 1 N
1018 5610736-150 LOGIQ V2/LOGIQ V1 User Guide Polish version 1 N
1019 5610736-151 LOGIQ V2/LOGIQ V1 User Guide Greek version 1 N
1020 5610736-153 LOGIQ V2/LOGIQ V1 User Guide Hungarian version 1 N
1021 5610736-154 LOGIQ V2/LOGIQ V1 User Guide Slovakian version 1 N
1022 5610736-155 LOGIQ V2/LOGIQ V1 User Guide Czech version 1 N
1023 5610736-159 LOGIQ V2/LOGIQ V1 User Guide Turkish version 1 N
1024 5610736-160 LOGIQ V2/LOGIQ V1 User Guide Danish version 1 N
1025 5610736-161 LOGIQ V2/LOGIQ V1 User Guide Norwegian version 1 N
1026 5610736-162 LOGIQ V2/LOGIQ V1 User Guide Finnish version 1 N

5610739-100 English Rev.10
Renewal Parts
Table 9-8: Manuals for LOGIQ V2/LOGIQ V1
1027 5610736-165 LOGIQ V2/LOGIQ V1 User Guide Bulgarian version 1 N
1028 5610736-167 LOGIQ V2/LOGIQ V1 User Guide Romanian version 1 N
1029 5610736-168 LOGIQ V2/LOGIQ V1 User Guide Croatian version 1 N
1030 5610736-174 LOGIQ V2/LOGIQ V1 User Guide Lithuanian version 1 N
1031 5610736-175 LOGIQ V2/LOGIQ V1 User Guide Latvian version 1 N
1032 5610736-176 LOGIQ V2/LOGIQ V1 User Guide Serbian version 1 N
1033 5610736-177 LOGIQ V2/LOGIQ V1 User Guide European 1 N

Portuguese version
1034 5610736-181 LOGIQ V2/LOGIQ V1 User Guide Indonesian version 1 N
1035 5610736-184 LOGIQ V2/LOGIQ V1 User Guide Kazakh version 1 N

5610739-100 English Rev.10
Chapter 10
Care and Maintenance
This chapter describes Care and Maintenance on the

Ultrasound system and peripherals. These procedures
are intended to maintain the quality of the Ultrasound
system’s performance. Read this chapter completely
and familiarize yourself with the procedures before
performing a task.

5610739-100 English Rev.10
Overview

• ‘Warnings’ on page 10-3
• ‘Why do maintenance’ on page 10-4
• ‘Maintenance task schedule’ on page 10-6
• ‘Tools required’ on page 10-8
• ‘System maintenance’ on page 10-12
• ‘Electrical safety tests’ on page 10-20
• ‘When there's too much leakage current …’ on page 10-31
• ‘Inspection Paperwork’ on page 10-33
• ‘Electrical Safety Tests Log’ on page 10-35

5610739-100 English Rev.10
Warnings
Warnings
DANGER BE SURE TO DISCONNECT THE ULTRASOUND SYSTEM

POWER PLUG AND OPEN THE MAIN CIRCUIT BREAKER
BEFORE YOU REMOVE ANY PARTS. BE CAUTIOUS
WHENEVER POWER IS STILL ON AND COVERS ARE
REMOVED.
CAUTION Practice good ESD prevention. Wear an anti–static strap when

handling electronic parts and even when disconnecting/
connecting cables.
CAUTION Do not pull out or insert circuit boards while power is on.
CAUTION Do not operate this Ultrasound system unless all board covers
and frame panels are securely in place. System performance
and cooling require this.

5610739-100 English Rev.10
Why do maintenance
Periodic maintenance inspections

It has been determined by engineering that your LOGIQ V2/
LOGIQ V1 does not have any high wear components that fail
with use, therefore no Periodic Maintenance inspections are
mandatory.
However, some customers’ Quality Assurance Programs may
require additional tasks and or inspections at a different
frequency than listed in this manual.
Keeping records
It is good business practice that ultrasound facilities maintain
records of periodic and corrective maintenance. The Ultrasound
Periodic Maintenance Inspection Certificate provides the
customer with documentation that the Ultrasound system is
maintained on a periodic basis.
A copy of the Ultrasound Periodic Maintenance Inspection
Certificate should be kept in the same room or near the
Ultrasound system.

5610739-100 English Rev.10
Why do maintenance
Quality assurance
In order to gain accreditation from organizations such as the
American College of Radiology (USA), it is the customer’s
responsibility to have a quality assurance program in place for
each Ultrasound system. The program must be directed by a
medical physicists, the supervising radiologist/physician or
appropriate designee.
Routine quality control testing must occur regularly. The same
tests are performed during each period so that changes can be
monitored over time and effective corrective action can be
taken.
Testing results, corrective action and the effects of corrective
action must be documented and maintained on the site.
Your GE service representative can help you with establishing,
performing and maintaining records for a quality assurance
program. Contact GE for coverage and/or price for service.

5610739-100 English Rev.10
How often should maintenance tasks be performed?

The Care and Maintenance task schedule (provided in
Table 10-1 on page 10-6) specifies how often your LOGIQ V2/
LOGIQ V1 should be serviced and outlines items requiring
special attention.
NOTE: It is the customer’s responsibility to ensure the LOGIQ V2/
LOGIQ V1 care and maintenance is performed as scheduled in
order to retain its high level of safety, dependability and
performance.
Your GE Service Representative has an in-depth knowledge of
your LOGIQ V2/LOGIQ V1 and can best provide competent,
efficient service. Contact GE for coverage information and/or
price for service.
The service procedures and recommended intervals shown in
the Care and Maintenance Task Schedule assumes that you
use your LOGIQ V2/LOGIQ V1 for an average patient load
(10-12 per day) and not use it as a primary mobile Ultrasound
system which is transported between diagnostic facilities.
NOTE: If conditions exist which exceed typical usage and patient load,
then it is recommended to increase the periodic maintenance
frequencies.
Table 10-1: Customer Care Schedule
Per
Facilities
Service at Indicated QA
Time Daily Weekly Monthly Program Notes
Clean Probes •* * or before each use
Inspect AC Mains Cable • Mobile Ultrasound

system: Check
Weekly
Inspect Cables and •

Connectors
Clean Console •

5610739-100 English Rev.10
Table 10-1: Customer Care Schedule (Continued)
Per
Facilities
Service at Indicated QA
Time Daily Weekly Monthly Program Notes
Clean LCD •
Console Leakage Current See Notes Twice Annually

Checks
Peripheral Leakage See Notes Twice Annually

Current Checks
Surface Probe Leakage See Notes Twice Annually

Current Checks
Endocavity Probe Leakage See Notes Quarterly Annually

Current Checks
Surgical Probe Leakage See Notes Quarterly Annually

Current Checks
Measurement See Notes Twice Annually

Accuracy Checks
Functional Checks See Notes also after corrective
maintenance
NOTE: The maintenance may require specialized equipment to

complete.
NOTE: The periodic maintenances are not mandatory. The table above
is for reference only.

5610739-100 English Rev.10
Tools required
NOTE: For a list of required tools for servicing the LOGIQ V2/LOGIQ
V1, refer to chapter 8.
Standard GE tool kit

The following is a description of the “Standard” GE tool kit in the
USA. Not all tools are required.
Table 10-2: Overview of GE-1 tool kit contents
Tool ID Description Tool ID Description
9-45358 Pliers Retaining Ring 9-XL9971MM Xcelite-hex Blade 1.27mm
9-4078 Scribe 9-XL9972MM Xcelite-hex Blade 1.5mm
9-44572 Wrench Open End 3/8 - 7/16 9-XL9973MM Xcelite-hex Blade 2 mm
9-44579 Wrench Open End 1/2 - 9/16 9-XL9974MM Xcelite-hex Blade 2.5mm
9-44579 Wrench Open End 1/2 - 9/16 9-XL9975MM Xcelite-hex Blade 3mm
9-45385 Pliers, Arc Joint 7 inch 9-XL9976MM Xcelite-hex Blade 4mm
9-45378 Pliers, Slip Joint 9-XL9977MM Xcelite-hex Blade 5mm
9-4518 Pliers, Long Nose, Miniature 9-XL991CM Handle
9-4518 Pliers, Long Nose, Miniature C2356E Screw starter - Kedman

Quick Wedge
9-44776 Ignition Wrench Set, 10 pc. BLBO Box - 18 Compartment
9-44601 Wrench, Adj., 4 inch DWL4283T Box - 5 Compartment
9-4151 Screwdriver, Blade, Stubby 9-41322 Pickup Tool, Claw type
9-41421 Screwdriver, Blade, Pocket 9-6757 6 pc Needle File Set

clip
9-41594 Screwdriver, Blade 1/8 in. × 4 9-9487 Utility Knife

in.
9-41581 Screwdriver, Blade 3/16 in. × 4 9-45341 Pliers Vice Grip 10 inch
in.
9-39451 20' Steel Tape, locking Spring 9-3001 Xacto Pen Knife
load

5610739-100 English Rev.10
Tools required
Table 10-2: Overview of GE-1 tool kit contents (Continued)
9-GH807 Ratchet, Offset, Slotted 9-HT62002 Solder Aid, Fork and Hook
68-412 Ratchet, Offset, Phillips 9-4099 Mirror, Round, Telescoping
9-GH130 Tapered Reamer 9-GH3001 Steel Rule Decimal 6 inch
9-41584 Screwdriver, slotted 1/4 in. × 6 9-GH300ME Steel Rule Metric 6 inch
in.
9-4118 Screwdriver, Phillips #2, 9-XL9920 Xcelite-hex Blade.050 inch

Stubby
9-41293 Screwdriver, Phillips #0 9-XL9921 Xcelite-hex Blade 1/16 inch
9-46677 Hex Keys, 20 pc., Metric 9-XL9924 Xcelite-hex Blade 1/8 inch
9-34701 1/4 in. Standard Socket set (19 9-XL9925 Xcelite-hex Blade 5/32 inch
pc)
9-43499 1/2 inch Socket 1/4 inch drive 9-XL9926 Xcelite-hex Blade 3/16 inch
9-4355 Flex Spinner 9-XL99764 Xcelite-hex Blade 7/64
9-43523 Breaker 9-XL99964 Xcelite-hex Blade 9/64
9-43531 6 inch Ext. 9-XLM60 Mini-screwdriver kit
9-65283 Case 8.5 in. × 4.5 in. × 2 in. 9-45072 Pliers 6 inch Diagonal
Deep
9-46696 Hex Keys 9-XL100X Wire Stripper/Cutter 5 inch -

100X
9-39829 Torpedo Level, Magnetic 9-XL87CG Pliers - very fine needle

nose-87CG
9-38461 Hammer, Ball Peen, 4 oz. 9-WEWDT-07 Weller-Soldering-Replacem

ent Tip(1)
9-4280 Universal Joint 1/4 inch 9-WS175-E Wiss - Surgical Scissors
9-WEW60P3 Weller - Soldering Iron, 3 wire KH174 Hemostat 5 inch Straight
9-WECT5B6 Weller - Soldering Iron Tip KH175 Hemostat 5 inch curved
9-WEWDP12 Weller - Desoldering Pump 9-Z9480121 Alignment tool (red)
93383 Flashlight Mini-Mag Lite (AAA

Bat.)
9-GH408 Tweezers
21576 Brush - Bristle

5610739-100 English Rev.10
Table 10-2: Overview of GE-1 tool kit contents (Continued)
9-4516 Pliers 4 1/4 inch Diagonal
GE-2 tool kit

Table 10-3: Overview of GE-2 tool kit contents
GE-2 Sears Kit (#99034)
9-45381 Pliers, Arc Joint 9 1/2 inch 9-44067 Socket 1 1/16 in. for 1/2 in.
drive
9-45092 Pliers, Linesman 8 1/2 inch 9-42679 Socket 10MM Hex for 1/2 in.
drive (2273333)
9-42882 Punch, Pin 3/32 inch 9-44262 Extension 10 inch for 1/2 in.
drive (2273405)
9-42884 Punch, Pin 5/32 inch 9-4258 3/8 inch to 1/2 inch Adapter
9-42886 Punch, Pin 1/4 inch 9-34374 3/8 inch Metric Socket Set -
12 PT
9-42973 Cold Chisel 1/2 inch 9-44311 16mm Socket 12 pt.
9-GH77 Center Punch Automatic 9-33485 Metal Socket Tray
9-GH890 File Handle, Adj. 9-33484 Metal Socket Tray
9-31276 File, Round, Bastard 8 inch 9-33484 Metal Socket Tray
9-31277 File, Half Round, Bastard 8 9-52068 Tap and Drill Set
inch
9-31263 File, Flat Mill 8 inch 9-52722 #6 Tap
21045C Close Quarter Saw 9-52723 #8 Tap
9-44604 Wrench, Adj. 10 inch High Speed Drill Set
9-41587 Screwdriver 5/16 inch × 8 inch #36 Drill
9-41586 Screwdriver, Stubby 5/16 inch #29 Drill
9-GH19512 Countersink 1/2 inch 9-44046 3/8 inch Socket Set
9-44741 12 PC Combination Wrench

Set

5610739-100 English Rev.10
Tools required
Special tools, supplies and equipment used for maintenance

Table 10-4: Overview of tool requirements for periodic maintenance
Tool / kit Comments
Digital Volt Meter (DVM)
Anti Static Kit Kit includes anti–static mat, wrist strap and cables
for 200 to 240V system
3M #2204 Large adjustable wrist strap
3M #2214 Small adjustable wrist strap
3M #3051 conductive ground cord
Anti Static Vacuum Cleaner 120V

230V
Safety Analyzer The safety Analyzer tool should be calibrated and

compliant with AAMI/ESI 1993 or IEC 60601 or
AS/NZS 3551.
QIQ Phantom RMI Grayscale Target Model 403GS

NOTE! The use of a Phantom is not required
during Preventive Maintenance. Customer may
use it as part of their Quality Assurance
Program tests.
B/W Printer Cleaning Sheet See printer user manual for requirements
Color Printer Cleaning Sheet See printer user manual for requirements
Disposable Gloves

5610739-100 English Rev.10
System maintenance
Preliminary checks
The preliminary checks take about 15 minutes to perform. Refer
to the Ultrasound system user documentation whenever
necessary.
Table 10-5: System preliminary checks
Step Item Description
1. Ask and Listen Ask the customer if they have any problems or questions about the
equipment.
2. Paperwork Fill in the top of Ultrasound Inspection Certificate (see Figure 10-6 on
page 10-33). Record all probes and Ultrasound system options.
3. Power up • Turn the Ultrasound system power on and verify that all fans and
peripherals turn on.
• Watch the displays during power up to verify that no warning or error
messages are displayed.
• Where applicable, confirm that the battery is charged. If no AC Input
present, use the internal battery.
4. Probes Verify that the Ultrasound system properly recognizes all probes.
5. Displays Verify proper display on the monitor.
6. InSite Where applicable, for Warranty and Contract Customers only:

• Verify that InSite is functioning properly.
• Ensure two-way remote communications.
7. Review Error Logs Where applicable, Error Logs can be reviewed via system diagnostics.
8. Diagnostics Optional.
9. Presets Backup all Customer Presets to an appropriate media.
10. Image Archive Back up the Image Archive onto appropriate media.

5610739-100 English Rev.10
System maintenance
Functional checks
NOTE: See also Chapter 4
The functional checks take about 60 minutes to perform. Refer
to the Ultrasound system user documentation whenever
necessary.
System checks
Table 10-6: System functional checks
1. B-Mode Verify basic B-Mode operation. Check the basic Ultrasound system
controls that affect this mode of operation.
2. CF-Mode Verify basic CF-Mode (Color Flow Mode) operation. Check the basic
Ultrasound system controls that affect this mode of operation.
3. Doppler Modes Verify basic Doppler operation (PW and CW if available). Check the basic
Ultrasound system controls that affect this mode of operation.
4. M-Mode Verify basic M-Mode operation. Check the basic Ultrasound system
controls that affect this mode of operation.
5. Probe Elements Perform an Element Test on each probe to verify that all the probe
elements and system channels are functional.
6. Applicable Verify the basic operation of all optional modes such as Contrast. Check
Software Options the basic Ultrasound system controls that affect each options operation.
7. Xmit/Recv Use the Visual Channel Utility on the loop connect to verify that all system
Elements xmit/recv channels are functional.
8. Operator Panel Perform the Operator Panel Test Procedure.

test
9. Keyboard Do the interactive keyboard test.
10. LCD Verify basic LCD display functions. Refer to Chapter 3 of the User Manual.
11. Software Menu Verify Software Menu display functions. Refer to Chapter 3 of the User
check Manual.
12. Peripherals See: ‘Peripheral checks’ on page 4-39.
13. Measurements In measurement mode, make distance measurement, get result in result
window. Verify the distance by graduate rule. Distance Accuracy should
be within ±5%. (Name result from result window Result A, result from
graduate rule Result B; Distance Accuracy = (Result B-Result A)/Result A)

5610739-100 English Rev.10
Peripheral/option checks
If any peripherals or options are not part of the system

configuration, the check can be omitted.
Refer to the User Manual for a list of approved peripherals/
options.
Table 10-7: GE approved peripheral/hardware option functional checks
1. Media Verify media drive(s) read/write property. Clean if necessary.
2. B/W Printer Verify hardcopy output of the B/W video page printer. Clean heads and
covers if necessary.
3. Color Printer Verify hardcopy output of the Color video page printer. Clean heads and
covers if necessary.
4. DICOM Verify that DICOM is functioning properly. Send an image to a DICOM

device.
5. ECG Verify basic operation with customer
6. Footswitch Verify that the footswitch is functioning as programed. Clean as necessary.
7. DVD Verify that the DVD is functioning properly. Clean heads and covers if
necessary.
Mains cable inspection
Table 10-8: Mains Cable Inspection, As Appropriate
1. Unplug Cord Disconnect the mains cable from the wall and Ultrasound system.
2. Inspect Inspect it and its connectors for damage of any kinds.
3. Verify Verify that the LINE, NEUTRAL and GROUND wires are properly attached
to the terminals, and that no strands may cause a short circuit.

5610739-100 English Rev.10
System maintenance
Cleaning
Table 10-9: General Cleaning
1. Console Remove the battery. Use a fluid detergent in warm water on a soft, damp
cloth to carefully wipe the entire system. Be careful not to get the cloth too
wet so that moisture does not enter the console.
2. Probe Holder Clean probe holders. (they may need to be soaked to remove excess gel).
3. LCD Use a soft, non-abrasive folder cloth. Gently wipe the LCD face. DO NOT
use a glass cleaner that has a hydrocarbon base (such as Benzene,
Methy Alcohol or Methy Ethyl Ketone) on LCD with the filter (anti-glare
shield).
Physical inspection
NOTE: These features may not be present on all Ultrasound systems.
Table 10-10: Physical checks
1. Labeling Verify that all Ultrasound system labeling is present and in readable
condition.
2. Scratches & Dents Inspect the exterior for dents, scratches or cracks.
3. Input Power Refer to: ‘Mains cable inspection’ on page 10-14.
4. Cables & Check all internal cable harnesses and connectors for wear and secure
Connectors connector seating. Pay special attention to footswitch assembly and probe
strain or bend reliefs.
5. Shielding & Check to ensure that all EMI shielding, internal covers, air flow panels and
Covers screws are in place. Missing covers and hardware could cause EMI/RFI
problems while scanning.
6. Control Panel Inspect keyboard and control panel. Note any damaged or missing items.
7. Control Panel Check for proper operation of all operator panel and Freeze Key light.
Lighting
8. LCD Inspect the LCD Display for scratches and bad pixels.
Verify proper operation of Contrast and Brightness controls.
Where applicable, confirm that the LCD arm allows:
• swivelling the screen to the left and to the right
• folding the screen to the locked position
• release and adjustment backwards and forwards
• can be adjusted in the up/down positions.
Note: LCD Arm movement may vary and is not applicable to all Ultrasound
systems.
9. External I/O Check all connectors for damage.

5610739-100 English Rev.10
Table 10-10: Physical checks (Continued)
10. Power and Check for proper operation of all Power and System Status Indicators.
System Status
Indicators
11. Battery Where applicable, check that the battery is not damaged, does not leak,
does not emit an odor, and is not deformed or discolored. Observe all
warnings and cautions for battery handling, recharging, storing, and/or
disposal,
Optional Diagnostic Checks

Optionally you can access the diagnostic software as described
in Chapter 5 or 7. View the error logs and run desired
diagnostics.
View the Log
1. Review the system error log for any problems.

2. Check the temperature log to see if there are any trends that
could cause problems in the future.
3. Check the Configuration Log; update if needed.

5610739-100 English Rev.10
System maintenance
Probe maintenance
Probe related checks
Table 10-11: System preliminary checks
1. Probe Holder Clean probe holders. (they may need to be soaked to remove excess gel).
2. Probes Thoroughly check the Ultrasound system probe connectors and remove
dust from inside the connector sockets if necessary. Visually check for
bent, damaged or missing pins.
3. Probes Verify that the Ultrasound system properly recognizes all probes.
Basic probe care
The Ultrasound system user manuals and various probe

handling cards provide a complete description of probe care,
maintenance, cleaning and disinfection. Ensure that you are
completely familiar with the proper care of GE probes.
Ultrasound probes can be easily damaged by improper
handling. See the User Manual and probe care cards for more
details. Failure to follow these precautions can result in serious
injury and equipment damage. Failure to properly handle or
maintain a probe may also void its warranty.
Any evidence of wear indicates the probe cannot be used.
Do a visual check of the probe pins and Ultrasound system
sockets before plugging in a probe.
The Interoperative probes often have special considerations and
individual probe user manuals. For Interoperative probes also
refer to their separate user manuals.

5610739-100 English Rev.10
Basic probe cleaning
Refer to the User’s Manual for details on probe cleaning.
WARNING To help protect yourself from blood borne diseases, wear

approved disposable gloves. These are made of nitrile derived
from vegetable starch to prevent allergic latex reactions.
CAUTION Failure to follow the prescribed cleaning or disinfection

procedures will void the probe’s warranty.
DO NOT soak or wipe the lens with any product not listed in the
User Manual. Doing so could result in irreparable damage to
the probe.
Follow care instructions that came with the probe.
CAUTION Disinfect a defective probe before you return it. Be sure to tag
the probe as being disinfected.

5610739-100 English Rev.10
System maintenance
Battery Performance Maintenance

Battery replacement every three years is recommended.
It is recommended to do battery performance maintenance one
time per year.
Please follow the flow chart below to carry out battery
performance maintenance.
Battery discharge
No
>45 minutes?
Yes
Battery charge > 3 hour Battery charge > 3 hour
No No
Battery power > 90%? Battery power > 90%?
Yes Yes
Replace battery Battery is Ok Discharge Replace battery
No
>45 minutes?
Yes
Battery is Ok Replace battery
Figure 10-1. Flow chart of Battery Performance Maintenance
NOTE: Disconnect all probes when discharge battery.

NOTE: Discharge the battery to let the system automatically shut down.

5610739-100 English Rev.10
Safety test overview

The electrical safety tests in this section are based on and
conform to IEC 60601-1 Medical Equipment Safety Standards.
They are intended for the electrical safety evaluation of
cord-connected, electrically operated, patient care equipment. If
additional information is needed, refer to the IEC 60601-1
documents
WARNING THE USER MUST ENSURE THAT THE SAFETY

INSPECTIONS ARE PERFORMED AT LEAST EVERY
12 MONTHS ACCORDING TO THE HISTORICAL
DATA. ONLY TRAINED PERSONS ARE ALLOWED TO
PERFORM THE SAFETY INSPECTIONS MENTIONED
ABOVE.
DANGER TO MINIMIZE RISK OF ELECTRICAL SHOCK, ONLY

TRAINED PERSONS ARE ALLOWED TO PERFORM THE
ELECTRICAL SAFETY INSPECTIONS AND TESTS.
DANGER TO AVOID ELECTRICAL SHOCK, THE ULTRASOUND

SYSTEM UNDER TEST MUST NOT BE CONNECTED TO
OTHER ELECTRICAL EQUIPMENT. REMOVE ALL
INTERCONNECTING CABLES AND WIRES. THE
ULTRASOUND SYSTEM UNDER TEST MUST NOT BE
CONTACTED BY USERS OR PATIENTS WHILE
PERFORMING THESE TESTS.
CAUTION Possible risk of infection. Do not handle soiled or contaminated

probes and other components that have been in patient
contact. Follow appropriate cleaning and disinfecting
procedures before handling the equipment.

5610739-100 English Rev.10
Safety test overview (continued)

Prior to initiating any electrical test, the Ultrasound system must
be visually inspected. Perform the following visual checks:
• Check for missing or loose enclosure covers that could
allow access to internal live parts.
• Examine the mains cord, mains plug and appliance inlet for
damaged insulation and adequacy of strain relief and cable
clamps.
• Locate and examine all associated transducers. Inspect the
cables and strain relief at each end. Inspect the transducer
enclosure and lens for cracks, holes and similar defects.
Test the system, peripherals and probes for leakage current.
Excessive leakage current can cause injury or death in sensitive
patients. High leakage current can also indicate degradation of
insulation and a potential for electrical failure. Do not use probes
or equipment having excessive leakage current.
To minimize the risk that a probe may shock someone the
customer should:
• Not use a probe that is cracked or damaged in any way.
• Check probe leakage current:
• Based on your facilities QA program for surface probes.
• Based on your facilities QA program for endocavitary
probes.
• whenever probe damage is suspected.

5610739-100 English Rev.10
Leakage current limits
CAUTION Compare all safety-test results with safety-test results of

previously performed safety tests (e.g. last year etc). In case of
unexplainable abrupt changes of safety-test results consult
experienced authorized service personnel or GE for further
analysis.
The following limits are summarized for IEC 60601-1 Medical

Equipment Safety Standards. These limits are GEMS standards
and in some cases are lower than the above standards listed.
Table 10-12: Chassis Leakage Current Limits - Accessible Metal Surface
Normal Reverse
Country Condition Open Ground Polarity Open Neutral
All (Except USA & 0.1 mA 0.5 mA 0.5 mA 0.5 mA

Canada)
USA & Canada 0.1 mA 0.3 mA 0.3 mA 0.3 mA
Table 10-13: Type BF Applied Part Leakage Current Limits - Probes Surface
Normal Open Reverse Open *Mains

Country Condition Ground Polarity Neutral Applied
All 0.1 mA 0.5 mA 0.5 mA 0.5 mA 5.0 mA

5610739-100 English Rev.10
Leakage current limits (continued)

Table 10-14: Type CF Applied Part Leakage Current Limits - ECG Connections
Normal Open Reverse Open *Mains

Country Condition Ground Polarity Neutral Applied
All 0.1 mA 0.5 mA 0.5 mA 0.5 mA 5.0 mA
NOTE: *Mains Applied refers to the sink leakage test where mains
(supply) voltage is applied to the part to determine the amount of
current that will pass (or sink) to ground if a patient contacted
mains voltage.
The following tests are performed at the factory and should be
performed at the site. These tests are: chassis leakage current,
and probe leakage current. All measurements are made with an
electrical safety analyzer which should be calibrated and
compliant with AAMI/ESI 1993 or IEC 60601 or AS/NZS 3551.
Table 10-15: Equipment Type and Test Definitions
Applied Parts or accessories that contact the patient to

Parts perform their function. For ultrasound equipment,
(AP) this includes transducers and ECG leads.
Type BF Body Floating or

non-conductive ultrasound
probes which are marked
with the 'man in box' BF
symbol. this includes all
transducers.
Type CF Cardiac Floating or

non-conductive
intraoperative probes for
direct cardiac contact and
isolated ECG connections
so marked with the 'heart in
box' CF symbol.
Sink The current resulting from the application of mains

Leakage voltage to the applied part. This test is required
test for Type CF applied parts.

5610739-100 English Rev.10
Outlet test - wiring arrangement

Test all outlets in the area for proper grounding and wiring
arrangement by plugging in the neon outlet tester and noting the
combination of lights that are illuminated. Any problems found
should be reported to the hospital immediately and the
receptacle should not be used.
CORRECT WIRING OPEN GROUND WIRE
REVERSED POLARITY OPEN NEUTRAL WIRE
HOT AND GROUND OPEN HOT WIRE

REVERSED
Figure 10-2. Typical alternate outlet tester
NOTE: No outlet tester can detect the condition where the Neutral
(grounded supply) conductor and the Grounding (protective
earth) conductor are reversed. If later tests indicate high leakage
currents, this should be suspected as a possible cause and the
outlet wiring should be visually inspected.

5610739-100 English Rev.10
Grounding continuity
DANGER ELECTRIC SHOCK HAZARD. THE PATIENT MUST NOT BE

CONTACTED TO THE EQUIPMENT DURING THIS TEST.
Measure the resistance from the third pin of the attachment plug
to the exposed metal parts of the case. The ground wire
resistance should be less than 0.2 ohms. Reference the
procedure in the IEC60601-1.
1. GROUND PIN
2. OHMMETER
3. LOGIQ V2/LOGIQ V1
4. ACCESSIBLE METAL PART:
• MONITOR HOUSING
• PEAR PANEL CONNECTOR
• ANY CASTER/WHEEL SUPPORT
Figure 10-3. Ground continuity test

5610739-100 English Rev.10
Chassis leakage current test
DANGER ELECTRIC SHOCK HAZARD. WHEN THE METER'S

GROUND SWITCH IS OPEN, DON'T TOUCH THE
ULTRASOUND SYSTEM!.
CAUTION Equipment damage possibility. Never switch the Polarity and

the status of Neutral when the Ultrasound system is powered
ON. Be sure to turn the Ultrasound system power OFF before
switching them using the POLARITY switch and/or the
NEUTRAL switch. Otherwise, the Ultrasound system may be
damaged.
Generic procedure
The test verifies the isolation of the power line from the chassis.
The testing meter is connected from accessible metal parts of
the case to ground. Measurements should be made with the unit
ON and OFF, with the power line polarity Normal and Reversed.
Record the highest reading of current.
Figure 10-4. Set Up for Chassis Source Leakage Current, IEC 601-1 Clause 19 -
Continuos Leakage Currents and Patient, Auxiliary Currents
When using the Microguard or a similar test instrument, its

power plug may be inserted into the wall outlet and the
equipment under test is plugged into the receptacle on the panel
of the meter. This places the meter in the grounding conductor
and the current flowing from the case to ground will be indicated
in any of the current ranges. The maximum allowable limit for
chassis source leakage is shown in Table 10-12 on page 10-22.

5610739-100 English Rev.10
Data Sheet for enclosure Source Leakage Current
The test passes when all readings measure less than the value
shown in Table 10-12 on page 10-22. Record all data on the PM
Inspection Certificate.
Table 10-16: Typical Data Sheet for enclosure Source Leakage Current
Tester
Neutral
Tester or Test 1 Test 2 Real
Unit Polarity Ground Speaker Panel Metal Optional Optional
Power Switch Switch Cover Parts Test 3 Test 4
Enter Name of tested peripheral here:
ON NORM OPEN
ON NORM CLOSED
ON REV OPEN
ON REV CLOSED
OFF NORM OPEN
OFF NORM CLOSED
OFF REV OPEN
OFF REV CLOSED

5610739-100 English Rev.10
Probe leakage current test
DANGER DO NOT USE THE PROBE IF THE INSULATING MATERIAL

HAS BEEN PUNCTURED OR OTHERWISE COMPROMISED.
INTEGRITY OF THE INSULATION MATERIAL AND PATIENT
SAFETY CAN BE VERIFIED BY SAFETY TESTING
ACCORDING TO IEC60601-1.
CAUTION Equipment damage possibility. Never switch the Polarity and

the status of Neutral when the Ultrasound system is powered
ON. Be sure to turn the Ultrasound system power OFF before
switching them using the POLARITY switch and/or the
NEUTRAL switch. Otherwise, the Ultrasound system may be
damaged.
Definition
This test measures the current that would flow to ground from
any of the probes through a patient who is being scanned and
becomes grounded by touching some other grounded surface.
NOTE: Some leakage current is expected on each probe, depending on
its design. Small variations in probe leakage currents are normal
from probe to probe. Other variations will result from differences
in line voltage and test lead placement. It is abnormal if no
leakage current is measured. If no leakage current is detected,
check the configuration of the test equipment.
Tools
For needed tools, see: ‘Tools required’ on page 10-8.

5610739-100 English Rev.10
Generic procedure on probe leakage current
Measurements should be made with the ground open and

closed, with power line polarity normal and reversed, and with
the unit Off and On. For each combination, the probe must be
active to find the worst case condition.
POLARITY REVERSING SWITCH

H (BLACK) PROBE
CONSOLE
POWER N (WHITE)
OUTLET
G (GREEN)
MOMENTARY
SWITCH LEAKAGE TEST
METER
Figure 10-5. Set up for probe leakage current
NOTE: Each probe will have some amount of leakage current,

dependent on its design. Small variations in probe leakage
currents are normal from probe to probe. Other variations will
result from differences in line voltage and test lead placement.
DANGER TO AVOID PROBE DAMAGE AND POSSIBLE ELECTRIC

SHOCK, DO NOT IMMERSE PROBES INTO ANY LIQUID
BEYOND THE LEVEL INDICATED IN THE PROBE USERS
MANUAL. DO NOT TOUCH THE PROBE, CONDUCTIVE
LIQUID OR ANY PART OF THE UNIT UNDER TEST WHILE
DOING THE TEST.
Meter Procedure Using Probe Adapter
Follow the Safety Analyzer tool instruction to test each

transducer for leakage current.
The electrical Safety Analyzer tool should be calibrated and
No Meter Procedure Using Probe Adapter
Follow the Safety Analyzer tool instruction to test each

transducer for leakage current.
The electrical Safety Analyzer tool should be calibrated and

5610739-100 English Rev.10
Data Sheet for Transducer Source Leakage Current
The test passes when all readings measure less than the values
shown in Table 10-13 on page 10-22. Record all data on the PM
Inspection Certificate.
Table 10-17: Typical Data Sheet For Transducer Source Leakage Current
Transducer Tested:
Tester Power Polarity Tester GROUND or

Unit Power Switch NUETRAL Switch Measurement
ON NORM OPEN
ON NORM CLOSED
ON REV OPEN
ON REV CLOSED
OFF NORM OPEN
OFF NORM CLOSED
OFF REV OPEN
OFF REV CLOSED

5610739-100 English Rev.10
When there's too much leakage current …
When there's too much leakage

current …
AC/DC Fails
Where applicable, check the AC/DC adapter and its cable.
Replace a new one if any portion is defective.
Chassis Fails
Check the ground on the power cord and plug for continuity.
Ensure the ground is not broken, frayed, or intermittent. Replace
any defective part.
Where applicable, tighten all grounds. Ensure star washers are
under all ground studs.
Inspect wiring for bad crimps, poor connections, or damage.
Test the wall outlet; verify it is grounded and is free of other
wiring abnormalities. Notify the user or owner to correct any
deviations. As a work around, check the other outlets to see if
they could be used instead.
NOTE: No outlet tester can detect the condition where the white neutral
wire and the green grounding wire are reversed. If later tests
indicate high leakage currents, this should be suspected as a
possible cause and the outlet wiring should be visually
inspected.

5610739-100 English Rev.10
Probe Fails
Test the probe in another connector to isolate if the fault lies with
the probe or the Ultrasound system. Or Change another probe
to confirm if the fail is caused by console.
NOTE: Each probe will have some amount of leakage, dependent on its
design. Small variations in probe leakage currents are normal
from probe to probe. Other variations will result from differences
in line voltage and test lead placement. The maximum allowable
leakage current for body surface contact probe differs from
inter-cavity probe. Be sure to enter the correct probe type in the
appropriate space on the check list.
If excessive leakage current is slot dependent, inspect the
system connector for bent pins, poor connections, and ground
continuity.
If the problem remains with the probe, replace the probe.
Peripheral Fails
Tighten all grounds. Ensure star washers are under all ground
studs.
Inspect wiring for bad crimps, poor connections, or damage.
Still Fails
If all else fails, begin isolation by removing the probes, external
peripherals, then the on board ones, one at a time while
monitoring the leakage current measurement.
New Unit
If the leakage current measurement tests fail on a new
Ultrasound system and if situation can not be corrected, submit
a Safety Failure Report to document the Ultrasound system
problem. Remove Ultrasound system from operation.
ECG Fails
Inspect cables for damage or poor connections.

5610739-100 English Rev.10
Ultrasound Inspection Forms
ULTRASOUND INSPECTION CERTIFICATE

C us tome r N a me : S y s te m I D : D is pa tc h N umbe r / Date Performed: Warranty/C ontract/HBS
System Type M ode l N umbe r: S e ria l N umbe r: M a nufa c ture D a te :
P robe 1 : F r e q u e nc y : S c a n F orma t*: M ode l N umbe r: S e ria l N umbe r:
* Scan Format: Phased Array, Linear Array, Curved Array, Mechanical Array or Other
Figure 10-6. Ultrasound Inspection Certificate
* Scan Format: Phased Array, Linear Array, Curved Array,

Mechanical Array or Other

5610739-100 English Rev.10
Ultrasound Inspection Forms (continued)
FUNCTIONAL CHECKS PHYSICAL INSPECTION AND CLEANING

OK? or Physical Inspection and Cleaning
Functional Check (if applicable) N/A (if applicable) Inspect Clean
B -Mode F unc tion C ons ole
D opple r Mode s F unc tion LC D
C F -Mode F unc tion E x te rna l I /O
M-Mode F unc tion C a ble s a nd C onne c tors
Applicable Software Opti ons G E A pprove d P e riphe ra ls (DVD-RW, Printer)
A pplic a ble H a rdwa re O ptions L a be ling (see User Manual for Labeling)
Control Panel
LCD
Measurement Accuracy
GE Approved Peripherals
COMMENTS:
_________________________ ____________________________ _________________________
_________________________ ____________________________ _________________________
_________________________ ____________________________ _________________________
_________________________ ____________________________ _________________________
Figure 10-7. Functional Checks
ELECTRICAL SAFETY
Max Value Value
Electrical Test Performed Allowed Measured OK? Comments
Outlet (correct ground &wiring config.)
Type BF Applied Part Leakage Current

Limits- Probe
enclosure Source Leakage Current -

Chassis Leakage Current Limits
Peripheral 1 Leakage Current
Peripheral 2 Leakage Current
PROBES
Probe Number Max Value Max Value

(from previous page) Allowed Measured OK? Comments
Probe 1:
Probe 2:
Probe 3:
Final Check. All system covers are in place. System scans with all probes as expected.
Accepted by: ______________________________________________________________________
Figure 10-8. Electrical Safety

5610739-100 English Rev.10
Table 10-18: Electrical safety tests log
Electrical test Max Value OK? Comments

performed value measured
allowed
Outlet (correct ground

and wiring config.)
System ground
continuity
Chassis source
leakage current -
probe
Chassis source
leakage current -
wheel
Chassis source
leakage current -
monitor
Patient lead source

leakage (lead to
ground)
Patient lead source

leakage (lead to lead)
Patient lead source

leakage (isolation)
Peripheral 1 leakage
current
Peripheral 1 ground
continuity
current

5610739-100 English Rev.10
Table 10-18: Electrical safety tests log (Continued)
Electrical test Max Value OK? Comments

performed value measured
allowed
Peripheral 2 ground
continuity
current
Peripheral 3 ground
continuity
Table 10-19: Electrical safety tests (probes) log
Max Max value OK? Comments

value measured
Probe allowed

5610739-100 English Rev.10
Index
A D
abbrevations, 9-3 damage
acclimate time, 2-3 in transportation, 3-7
authorized representative in EU, 1-29 damage in transport, i-14
average setup time, 3-3 dangerous procedure warnings, 1-22
data network setup requirements, 2-19
B desirable features, 2-15
DICOM network function, 2-19
before installation (site preparations), 2-1 DICOM setup requirements, 2-20
Boot Up, 3-17 display PDF files
from manual CD-ROM
C print PDF files
from manual CD-ROM, 4-21
cable inspection
mains cable inspection, 10-14 E
care and maintenance, 10-1
warnings, 10-3 electrical requirements, 2-6
CE compliance, 1-25 EMI limitations
change history, i-1 EMI limitations, 2-9
chapter 1 general requirements, 2-6
introduction, 1-1 site circuit breaker
chassis leakage current test, 10-26 site circuit breaker, 2-7
cold or hot site power outlets
if the unit is very cold or hot, 2-3 site power outlets, 2-7
compatibility specific requirements for the unit, 2-6
hardware/software, 9-4 unit power plug
completing the setup, 3-14 unit power plug, 2-7
compliance, 1-25 electrical safety, 1-18
configuration, 3-18 electrical safety tests, 10-20
connect electrical specification, 3-15
probe, 3-17 electromagnetic interference
connections abatement, 2-10
on the rear panel, 3-16 prevention, 2-10
console environmental requirements, 2-3 electrostatic discharge prevention, 1-26
console requirements, 2-3 EMC, 1-25
contact information, 1-27 compliance, 1-25
contents in this manual, 1-3 what is EMC?, 1-25
conventions used in book, 1-6 EMI, 1-25
cooling, 2-5 abatement, 2-10
copyrights, i-17 prevention, 2-10
customer assistance, 1-27 protection, 3-13
phone numbers, 1-28 environmental dangers, 2-22
customer order environmental specifications for the unit, 2-4
verification, 3-13 errors, i-15
customer provided prerequisite, 7-13 ESD, 1-25
ESD prevention, 1-26
examine packages, 3-6
LOGIQ V2/LOGIQ V1 – Basic Service Manual Index-1

5610739-100 English Rev.10
external I/O list of abbrevations, 9-3
connections, 3-16 loading software, 7-13
lockout/tagout (LOTO) requirements, 1-23
F LOTO
lockout/tagout requirements, 1-23
facility needs, 2-12
desirable features, 2-15 M
DICOM network function, 2-19
DICOM setup requirements, 2-20 mains cable inspection, 10-14
InSite requirements, 2-19 maintenance
network setup requirements, 2-19 physical inspection, 10-15
purchaser responsibilities, 2-13 preliminary checks, 10-12
recommended floor plan suggestion, 2-17 system maintenance, 10-12
required facility needs, 2-14 maintenance task schedule, 10-6
suggested floor plan manufacturer, 1-28
scanner and EchoPAC in same room, 2-18 mass
floor plan suggestion with monitor and peripherals, 3-14
recommended, 2-17 mechanical safety, 1-16
scanner and EchoPAC in same room, 2-18 model designations, 1-6
functional checks, 10-13 models covered by this manual, 1-5
mains cable inspection, 10-14
system checks, 10-13 N
G network setup requirements, 2-19
GE Healthcare leakage current limits, 10-22 O

general console requirements, 2-3
generic procedure on probe leakage current, 10-29 omission and errors, i-15
grounding continuity, 10-25 operational and storage temperature for probes, 2-11
H P
hardware/software compatibility, 9-4 packing materials
hardware-software recycling information, 3-12
compatibility, 5-3 paperwork
hot or cold after setup, 3-42
if the unit is very cold or hot, 2-3 PDF files
how often should maintenance tasks be performed?, display and print, 4-21
10-6 periodic maintenance inspection (PM), PM (periodic
human safety, 1-13 maintenance inspection), 10-4
phone numbers
I customer assistance, 1-28
physical dimensions, 3-14
icons, 1-6 physical inspection
icons indicating a special procedure to be used, 1-9 at arrivel, 3-13
if the unit is very cold or hot, 2-3 Power On, 3-17
important precautions, i-2 precautions
InSite certified electrical contractor statement, i-14
network requirements, 2-19 damage in transport, i-14
installation important precautions, i-2
see "system setup", 3-1 service safety considerations, i-16
installation warnings translation policy, i-2
see "setup warnings", 3-3 prepeare for setup, 3-13
introduction (chapter 1), 1-1 prerequisite
provided by customer, 7-13
L probe
connect, 3-17
legal notes, i-17 probe cleaning, 10-18
lighting, 2-5 probe leakage current test, 10-28
Index-2 LOGIQ V2/LOGIQ V1 – Basic Service Manual

5610739-100 English Rev.10
probe maintenance, 10-17 physical inspection, 10-15
basic probe care, 10-17 preliminary checks, 10-12
basic probe cleaning, 10-18 system manufacturer, 1-28
probe related checks, 10-17 system requirements verification, 3-14
probe related checks, 10-17 system setup, 3-1
probes environmental requirements, 2-11
operational and storage temperature for probes, T
2-11
product icons, 1-10 time and manpower requirements
product locator installation card, 3-42 site preparations, 2-11
products covered by this manual, 1-5 tools required, 10-8
Purchaser responsibilities, 2-13 special tools, supplies and equipment, 10-11
standard GE tool kit, 10-8
R trademarks, i-17
translation policy, i-2
rear panel transport
connections, 3-16 damage, i-14
receiving and unpacking, 3-6 typical users of the service manual, 1-4
receiving the product, 3-6
recycling information U
packing materials, 3-12
required facility needs, 2-14 unpacking, 3-6
requirements, 2-3 unpacking instructions, 3-8
requirements verification, 3-14
returning/shipping probes and repair parts, 1-24 V
revision history, i-1
verification
S system requirements, 3-14
verify customer order, 3-13
safety voltage settings, 3-15
human, 1-13
safety precaution messages, 1-7 W
safety test overview, 10-20
service safety considerations, i-16 warnings, 10-3
dangerous procedures, 1-22
setup
receiving and unpacking, 3-6
completion, 3-14
preparations, 3-13 what is EMC?, 1-25
when there’s too much leakage current, 10-31
reminders, 3-3
chassis fails, 10-31
setup time, 3-3
setup warnings, 3-3 new unit, 10-32
peripheral fails, 10-32
shipping/returning probes and repair parts, 1-24
probe fails, 10-32
site preparations, 2-1
time and manpower requirements, 2-11 still fails, 10-32
software loading, 7-13
software/hardware compatibility, 9-4
software-hardware
compatibility, 5-3
specifications, 3-14
electrical specifications, 3-15
physical dimensions, 3-14
standard GE tool kit, 10-8
standard hazard icons, 1-8
statement
certified electrical contractor statement, i-14
system
specifications, 3-14
system checks, 10-13
system maintenance, 10-12
LOGIQ V2/LOGIQ V1 – Basic Service Manual Index-3

5610739-100 English Rev.10
Index-4 LOGIQ V2/LOGIQ V1 – Basic Service Manual
5610739-100 English Rev.10
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All Material Copyright © 2015-2017 by General Electric Company Inc.

Copyright © 2015-2017, General Electric Company.

Rev.2 2015/11/13 New software version, general update

Rev.3 2015/11/23 Add software wipe information

Rev.4 2016/01/05 Update spare part list

Rev.5 2016/02/18 Update spare part list

Rev.6 2016/06/15 Update spare part list

Rev.7 2016/11/21 Change safety test frequency

Rev.8 2017/02/23 Update software loading procedure

Rev.9 2017/08/23 Update spare part list

Rev.10 2017/10/31 Add ECG Installation

List of Effected Pages (LOEP)

Chapter Revision Chapter Revision

Front Rev.10 Chapter 6 Rev.10

Front matter Rev.10 Chapter 7 Rev.10

TOC Rev.10 Chapter 8 Rev.10

Chapter 1 Rev.10 Chapter 9 Rev.10

Chapter 2 Rev.10 Chapter 10 Rev.10

Chapter 3 Rev.10 Index Rev.10

Chapter 4 Rev.10 Rear Cover Rev.10

LOGIQ V2/LOGIQ V1 – Basic Service Manual i-1

i-2 LOGIQ V2/LOGIQ V1 – Basic Service Manual

Certified electrical contractor statement - For USA Only

i-14 LOGIQ V2/LOGIQ V1 – Basic Service Manual

GE employees should use TrackWise to report service

LOGIQ V2/LOGIQ V1 – Basic Service Manual i-15

DANGER DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH,

WARNING Use all Personal Protection Equipment (PPE) such as gloves,

For a complete review of all safety requirements, refer to

i-16 LOGIQ V2/LOGIQ V1 – Basic Service Manual

LOGIQ V2/LOGIQ V1 – Basic Service Manual i-17

Translation policy - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-2

LOGIQ V2/LOGIQ V1 – Basic Service Manual i-19

i-20 LOGIQ V2/LOGIQ V1 – Basic Service Manual

LOGIQ V2/LOGIQ V1 – Basic Service Manual i-21

i-22 LOGIQ V2/LOGIQ V1 – Basic Service Manual

LOGIQ V2/LOGIQ V1 – Basic Service Manual i-23

i-24 LOGIQ V2/LOGIQ V1 – Basic Service Manual

LOGIQ V2/LOGIQ V1 – Basic Service Manual i-25

This chapter describes important issues related to

LOGIQ V2/LOGIQ V1 – Basic Service Manual 1-1

Contents in this chapter

1-2 LOGIQ V2/LOGIQ V1 – Basic Service Manual

This manual provides installation and service information for the

Contents in this manual

Table 1-1: Contents in this manual

Chapter Chapter title Description

LOGIQ V2/LOGIQ V1 – Basic Service Manual 1-3

Table 1-1: Contents in this manual (Continued)

Chapter Chapter title Description

Typical users of the Proprietary Service Manual

1-4 LOGIQ V2/LOGIQ V1 – Basic Service Manual

LOGIQ V2/LOGIQ V1 models covered by this manual

Table 1-2: LOGIQ V2/LOGIQ V1 Model Designations

Model Number Description System SW

5661244 LOGIQ V2 Generic version R1.x.x

5661242 LOGIQ V1 Generic version R1.x.x

NOTE: When not otherwise specified, the contents of this manual