GE LOGIQ V1_V2 Basic Service Manual_SM_5610739-100_10 OZONE DISINFECTION SYSTEM OPERATION & MAINTENANCE MANUAL MODEL: 0077-0010

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: [phone]; FAX: [phone]
www.gehealthcare.com

Revision history

Revision History

Date

Revision

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.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

(YYYY/MM/DD)

List of Effected Pages (LOEP)

Reason for change

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.

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Important precautions

Translation policy

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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.

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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

information to:

GE Medical Systems (China) Co., Ltd.
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.

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Service Safety Considerations

WARNING

DANGER DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH,

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

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

For a complete review of all safety requirements, refer to
Chapter 1 in the Service Manual.

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Legal notes

Trademarks

Copyrights

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.

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

All Material Copyright © 2015-2017 by
General Electric Company Inc. All Rights Reserved.

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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

Table of Contents

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Authorized Representative- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-29

Chapter 2 — Site Preparations

Overview

Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-2

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

Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-2

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

Purpose of this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-18
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
Contents in 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

Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-2

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

Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-2

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

Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-2

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

Purpose of this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-13
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

Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-2

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

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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

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Inspection Paperwork

Ultrasound Inspection Forms - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-33

Electrical Safety Tests Log

Index

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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.

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Introduction

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

Overview

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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).

Manual Overview

Manual Overview

Chapter
number

1.

2.

3.

4.

5.

6.

An Index has been included after Chapter 10.

Table 1-1: Contents in this manual

Chapter title Description

Introduction Contains a content summary and warnings.

Site preparations Contains pre-setup requirements for the LOGIQ

V2/LOGIQ V1.

System Setup Contains setup procedure with procedure

checklist for the system.

General Procedures
and Functional
Checks

Components and
Functions (Theory)

Service Adjustments Contains instructions on how to make any

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

Contains block diagrams and functional
explanations of the electronics.

available adjustments to the LOGIQ V2/LOGIQ
V1.

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Introduction

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

Chapter

Chapter title Description

number

7.

8.

9.

Diagnostics/
Troubleshooting

Replacement
procedures

Provides procedures for running diagnostic or
related routines for the LOGIQ V2/LOGIQ V1.

Provides disassembly procedures and
reassembly procedures for all changeable FRU.

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

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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

Important conventions

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.

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Safety precaution messages

DANGER

WARNING

CAUTION

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

Warning is used to indicate the presence of a hazard that can
cause severe personal injury and property damage if
instructions are ignored.

Important conventions

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.

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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.

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Important conventions

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.

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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.

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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

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Introduction

Label/Icon Purpose/Meaning Location

Table 1-5: Label Icons

Every system has a unique
marking for identification, the
Unique Device Identification
(UDI) Label. The UDI label
consists of a series of
alpha-numeric characters and
barcode which uniquely identify
the 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

Rating plate

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Contents in this section

DANGER

WARNING

• ‘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.

Safety considerations

Safety considerations

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.

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

If the covers are removed from an operating LOGIQ V2/LOGIQ
V1, some metal surfaces may be warm enough to pose a
potential heat hazard if touched, even while in shutdown mode.

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Introduction

WARNING

WARNING

WARNING

WARNING

Human Safety (continued)

Explosion Warning

DO NOT operate the equipment in an explosive atmosphere.
Operation of any electrical equipment in such an environment
constitutes a definite safety hazard.

DO NOT substitute parts or modify equipment

Because of the danger of introducing additional hazards, ONLY
install GE approved parts. DO NOT perform any unauthorized
modification of the equipment.

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

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

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Human Safety (continued)

WARNING

WARNING

WARNING

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

Beware of possible sharp edges on all mechanical parts. If
sharp edges are encountered, the appropriate PPE should be
used to reduce the risk of injury.

Wear all PPE including gloves as indicated in the chemical
MSDS.

Safety considerations

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Introduction

WARNING

WARNING

WARNING

CAUTION

Mechanical safety

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.

Ultrasound probes are highly sensitive medical instruments
that can easily be damaged by improper handling. Use care
when handling and protect from damage when not in use. Do
NOT use a damaged or defective probe. Failure to follow these
precautions can result in serious injury and equipment
damage.

Never use a probe that has fallen to the floor. Even if it looks
OK, it may be damaged.

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.

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Mechanical safety (continued)

WARNING

CAUTION

CAUTION

CAUTION

CAUTION

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.

Use protective glasses during drilling, filing smooth surfaces,
and during all other work where eyes need protection.

Use safety shoes when doing work where there is any chance
of foot injury.

Safety considerations

Use protective gloves when working with sharp edges or when
directed to wear PPE during a removal/replacement procedure.

Be careful not to pinch any of the cables.

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Introduction

WARNING

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

Connecting a LOGIQ V2/LOGIQ V1 to the wrong voltage level
will most likely destroy it.

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Probes

Peripherals

Safety considerations

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.

Refer to the Patient Safety Environment section of the User’s
Manual for peripheral isolation information.

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Introduction

WARNING

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.

• 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.

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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

• 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°

• When charging for the first time after long-term

• When store packs for more than 6 months, charge at

Safety considerations

(23° F) and 50° C (122°F).

F) and 50° C (122°F).

storage. Recover such packs to original performance
through repeating several cycles of full charging and
discharging.

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.

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Introduction

DANGER

WARNING

WARNING

WARNING

WARNING

Dangerous procedure warnings

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

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

If the covers are removed from an operating LOGIQ V2/LOGIQ
V1, some metal surfaces may be warm enough to pose a
potential heat hazard if touched, even while in shutdown mode.

Explosion Warning

DO NOT operate the equipment in an explosive atmosphere.
Operation of any electrical equipment in such an environment
constitutes a definite safety hazard.

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.

SHUT DOWN FORCEDLY OR PLUG IN/OUT ACDC
INVALID MAY CAUSE THE DAMAGE OF SYSTEM
FILES.

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Lockout/Tagout (LOTO) requirements

WARNING

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.

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.

6. Remove/disconnect the battery, if present.

Ultrasound System components may be energized.

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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.

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What is EMC?

EMC, EMI and ESD

EMC, EMI and ESD

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.

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5610739-100 English Rev.10

Introduction

WARNING

WARNING

Electrostatic discharge (ESD) prevention

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.

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.

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Contact information

Customer assistance

Customer assistance

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.

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Introduction

Phone numbers for Customer Assistance

Table 1-6: Phone numbers for Customer Assistance

LOCATION PHONE NUMBER

USA
GE Healthcare - GE Medical Systems
Ultrasound Service Engineering
9900 Innovation Drive
Wauwatosa, WI 53226

Canada Phone: [phone]

Latin America Service

Europe (OLC-EMEA)
GE Ultraschall Deutschland Gmbh & Co. KG
Beethovenstraße 239
Postfach 11 05 60, D-42655 Solingen
Germany

Online Services Ultrasound Asia Phone:

Service: On-site 1-800-437-1171

Service Parts 1-800-558-2040

Application Support 1-800-682-5327 or

1-262-524-5698

Application Support

OLC - EMEA
Phone:

Fax: [phone]

• Australia

• China

• India

• Japan

• Korea

• Singapore

1-800-321-7937
1-262-524-5698

[phone] - 652
[phone]

+(61) 1-800-647-855
+(86) 800-810-8188
+(91) 1800-425-8025
+(81) 42-648-2940
+(82) 2620 13585
+(95) 6277-3444

System manufacturer

Table 1-7: System manufacturer

MANUFACTURER PHONE NUMBER FAX NUMBER

GE Medical Systems (China) Co., Ltd.
No.19 Changjiang Road
WuXi National Hi-Tech Development Zone
Jiangsu
P.R.China 214028

[phone] [phone]

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Authorized Representative

Table 1-8: Authorized Representative

AUTHORIZED REPRESENTATIVE

Customer assistance

TELEPHONE / FAX

NUMBER

The location of the CE marking is shown in the Safety chapter of the User
manual.

Authorized EU Representative/European registered place of business:
GE Medical Systems Information Technologies GmbH (GEMS IT GmbH)
Munzinger Strasse 5, D-79111 Freiburg, GERMANY

[phone] /
[phone]

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Introduction

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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.

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

Contents in this chapter

• ‘Overview’ on page 2-2

• ‘General Ultrasound system requirements’ on page 2-3

• ‘Facility needs’ on page 2-12

• ‘Environmental Dangers’ on page 2-22

Overview

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General Ultrasound system

CAUTION

Contents in this section

• ‘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

General Ultrasound system requirements

requirements

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.

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

000000246

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Site Preparations

CAUTION

CAUTION

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

50° - 104°F

Humidity 30 - 80%

non-condensing

Pressure 700 - 1060hPa 700 - 1060hPa 700 - 1060hPa

Ensure that the probe face temperature does not exceed the
normal operation temperature range.

The LOGIQ V2/LOGIQ V1 system and probe connector is not
waterproof. Do not expose the device to water or any kind of
liquid.

-5° - 50°C

23° - 122°F

10 - 90%
non-condensing

-5° - 50°C

23° - 122°F

10 - 90%
non-condensing

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Cooling

Lighting

General Ultrasound system requirements

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.

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.

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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

Vol tag e

To le r an c e Power Consumption Frequency

:

:

100-240 VAC ±10% Max. 200VA 50/ 60HZ

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Site circuit breaker

CAUTION

CAUTION

Site power outlets

General Ultrasound system requirements

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.

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.

Unit power plug

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.

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.

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Site Preparations

Power stability requirement

Table 2-4: Power stability requirement

IEC 61000-4-11

Voltage dips, short
interruptions and
voltage variations
on mains supply

< 5%T (> 95% dip) for

0.5 cycle;

40%T (60% dip) for 5
cycles;

70%T (30 dip) for 25
cycles;

< 5%T (>95% dip) for 5
sec

< 5%T (> 95% dip) for

0.5 cycle;

40%T (60% dip) for 5
cycles;

70%T (30 dip) for 25
cycles;

< 5%T (>95% dip) for 5
sec

Mains power
quality should be
that of a typical
commercial or
hospital
environment.

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EMI limitations

General Ultrasound system requirements

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.

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Site Preparations

EMI prevention/abatement

Table 2-5: EMI prevention/abatement

EMI RULE DETAILS

Be aware of Radio
Frequency sources

Ground the
Ultrasound system

Replace all screws,
Radio Frequency
gaskets, covers,
cores

Replace broken
Radio Frequency
gaskets

Do not place labels
where Radio
Frequency gaskets
touch metal

Use GE specified
harnesses and
peripherals

Take care with
cellular phones

Properly route
peripheral cables

• Keep the Ultrasound system at least 5 meters (15 feet) away from other EMI
sources.

• Special shielding may be required to eliminate interference problems caused by
high frequency, high powered radio or video broadcast signals.

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

• After you finish repairing or updating the Ultrasound system, replace all covers
and tighten all screws.

• Any cable with an external connection requires a magnet wrap at each end.

• Install all covers. Loose or missing covers or Radio Frequency gaskets allow
radio frequencies to interfere with the ultrasound signals.

If more than 20% or a pair of the fingers on an Radio Frequency gasket are
broken, replace the gasket. Do not turn on the Ultrasound system until any loose
metallic part is removed.

Where applicable, never place a label where Radio Frequency gaskets meet the
Ultrasound system. Otherwise, the gap created will permit Radio Frequency
leakage. Or, if a label has been found in such a position, move the label.

The interconnect cables are grounded and require ferrite beads and other
shielding. Also, cable length, material, and routing are all important; do not change
from what is specified.

Cellular phones may transmit a 5 V/m signal; that could cause image artifacts.

Where applicable, do not allow cables to lie across the top of the Card Rack or
hang out of the peripheral bays. Loop the excess length for peripheral cables
inside the peripheral bays. Attach the monitor cables to the frame.

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General Ultrasound system requirements

CAUTION

CAUTION

CAUTION

Probes environmental requirements

Operation, storage and transport temperatures for probes

Probes should be operated, stored, or transported within the
parameters outlined below.

Ensure that the probe face temperature does not exceed the
normal operation temperature range.

Table 2-6: Probe Environmental Requirements

Operational Storage Transport

Temperature 10° - 40° C

50° - 104° F

Humidity 30- 80%

non-condensing

Pressure 700 - 1060hPa 700 - 1060hPa 700 - 1060hPa

-5° - 50° C
23° - 122° F

10 - 90%
non-condensing

-5° - 50° C
23° - 122° F

10 - 90%
non-condensing

Check the room temperature before you use the probe.

Ensure that the probe face temperature does not exceed the
normal operation temperature range.

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.

LOGIQ V2/LOGIQ V1 – Basic Service Manual 2-11
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Site Preparations

Contents in this section

• ‘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

Facility needs

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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.

Facility needs

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.

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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.

:

:

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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)

Facility needs

Desirable features

For the amperage requirements, see: ‘Electrical requirements’
on page 2-6.

• Door is at least 92 cm (3 ft.) wide

• Circuit breaker for dedicated power outlet is easily
accessible

• Sink with hot and cold water

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

• Emergency oxygen supply

• Storage for linens and equipment

• Nearby waiting room, lavatory, and dressing room

• Dual level lighting (bright and dim)

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

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Site Preparations

4

1

3

11

6

13

8

10

5

7

9

12

14

2

Minimal floor plan suggestion

CSI 8x10

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

1. Door – at least 762 mm (30
inches)

2. Film Viewer

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

4. Linen Supply

5. Probes/Supplies

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

7. Footswitch

8. Stool

9. Ultrasound system

10. External Peripherals

11. Dedicated Power Outlet ­Circuit Breaker protected and
easily accessible

12. Network Interface

13. 457 mm (18 inches) distance
of Ultrasound system from
wall or objects

14. GE Cabinet for Software and
Manuals

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

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Recommended floor plan suggestion

CSI 14x17

Facility needs

10

11

12

15

9

2

3

4

5

13 14

16

8

7

1

17

6

18

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

1. Secretaries or Doctors Desk

2. File Cabinet

3. Film Viewer

4. Counter Top

5. Counter Top and Sink with
hot and cold water

6. Overhead Lights Dimmer ­Dual Level Lighting (bright
and dim)

7. Emergency Oxygen

8. Suction Line

9. Ultrasound system

10. Dedicated Power Outlet ­Circuit Breaker protected and
easily accessible

11. Network Interface

12. 457 mm (18 inches) distance
of Ultrasound system from
wall or objects

13. Stool

14. Footswitch

15. Storage for Linens and
Equipment

16. Examination Table – 1930 x
610 mm (76 x 24 inches)

17. Lavatory and Dressing Room

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

Figure 2-2. A 14 by 17 foot recommended floor plan

LOGIQ V2/LOGIQ V1 – Basic Service Manual 2-17
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Site Preparations

Suggested floor plan, Ultrasound system, and EchoPAC PC in same

room

1. EchoPAC PC workstation
parts

2. UPS

3. Ethernet network wall outlet

4. 3x mains power outlets

5. Hot and Cold water

6. Dedicated mains power out­let

7. Ethernet network wall outlet

Figure 2-3. Suggested Room with EchoPAC PC workstation and Ultrasound Scanner

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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

Facility needs

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.

LOGIQ V2/LOGIQ V1 – Basic Service Manual 2-19
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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.

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DICOM option setup requirements (continued)

Facility needs

Figure 2-4. Worksheet for DICOM Network Information

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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

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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.

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System Setup

Contents in this chapter

• ‘Overview’ on page 3-2

• ‘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

Overview

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Average setup time

DANGER

CAUTION

CAUTION

CAUTION

Setup warnings

Setup reminders

Setup reminders

• 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.

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!

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.

DO NOT wear the ESD wrist strap when you work on live
circuits and more than 30 V peak is present.

DO NOT operate this unit unless all board covers and frame
panels are securely in place. System performance and cooling
require this.

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System Setup

DANGER

CAUTION

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.

Equipment damage possibility. Turning the system on without
acclimation after arriving at site may cause the system to be
damaged.

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 420000000246

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Setup warnings (continued)

CAUTION

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.

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.

Setup reminders

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System Setup

CAUTION

Receiving and unpacking the

Purpose of this section

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

Contents in this section

• ‘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

equipment

Warnings for receiving and unpacking

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.

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Damage in transportation

Follow this procedure if damage is apparent:

1. Write “Damage In Shipment” on ALL copies of the freight or

2. Report the damage to the carrier.

Receiving and unpacking the equipment

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.

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System Setup

CAUTION

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

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

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Receiving and unpacking the equipment

CAUTION

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

Do not lift the unit by the rubber band. Equipment damage
may result.

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System Setup

Unpacking the LOGIQ V2/LOGIQ V1 (continued)

5. Remove 2 interleavers.

6. Remove plastic bag.

Figure 3-3. Removing interleavers and plastic bag

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Receiving and unpacking the equipment

CAUTION

CAUTION

Unpacking the LOGIQ V2/LOGIQ V1 (continued)

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

Do not lift the unit by the rubber band. Use handle to move
system.

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.

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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).

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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.

Preparing for setup

Preparing for setup

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.

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System Setup

Purpose of this section

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

Contents in this section

• ‘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

Completing the setup

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

4.72 15.59 14.49

Console Weight

• Weight: approx. 6 kg (13.23 lbs)

mm

Inches

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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

Completing the setup

Part

Number

5661244 LOGIQ V2 Generic

5661242 LOGIQ V1 Generic

Description Vol tag e Tol era nce s

version

version

Power

consumntion

100-240V ±10% Max.200VA 50/60 Hz

Frequency

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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

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Completing the setup

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.

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System Setup

System Configuration

Purpose of this section

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.

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Peripherals Installation

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

Peripherals Installation

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

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System Setup

Furnished materials

Item Description Quantity Note

1 Sony UP-D897 Printer 1

2 Sony UP-D898MD Printer 1

3 Paper Roll 1

4 USB cable 1

Table 3-6: Materials furnished with Color USB Printer

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

• Color USB Printer

Item Description Quantity Note

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

Item Description Quantity Note

1 HP Officejet 100 Printer 1

2 HP Officejet Pro 8100 Printer 1

3 Paper Roll 1

4 USB cable 1

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