General Electric LOGIQ E R6 BASIC SERVICE MANUAL_SM_5461614-100_6 Technical Publication LOGIQ e Basic Service Manual Direction Number: 5461614-100 English Rev. 6

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Technical Publication

LOGIQ e

Basic Service Manual Direction Number: 5461614-100 English

Rev. 6

Product Information

This Manual covers the software version of R8.x.x for LOGIQ e ultrasound system.

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

REV

Rev.1 2013/06/07 Initial Release

Rev.2 2013/10/10 Add service information

Rev.3 2014/03/07 Update spare part list

Rev.4 2014/05/12 Add E-Isolation Cart spare parts

(YYYY/MM/DD) REASON FOR CHANGE

Rev.5 2014/09/26 1. Add barcode scanner setting up information

Rev.6 2015/02/11 Add Advanced Isolation Cart spare part information

2. Add system date and time check information

3. Add external monitor connection methods from Docking Cart

4. Update spare part list

List of Effected Pages (LOEP)

Pages Revision Pages Revision

Front Rev. 6 Chapter 7 Rev. 6

Front matter Rev. 6 Chapter 8 Rev. 6

TOC Rev. 6 Chapter 9 Rev. 6

Chapter 1 Rev. 6 Chapter 10 Rev. 6

Chapter 2 Rev. 6 Chapter 11 Rev. 6

Chapter 3 Rev. 6 Chapter 12 Rev. 6

Chapter 4 Rev. 6 Index Rev. 6

Chapter 5 Rev. 6 Rear Cover Rev. 6

Chapter 6 Rev. 6

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 Changjiang 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

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

Proprietary to GE

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.

Permission to use this Advanced Service Software and related documentation (herein called the material) by persons other than GE employees is provided only under an Advanced Service Package License relating specifically to this Proprietary Material. This is a different agreement from the one under which operating and basic service software is licensed. A license to use operating or basic service software does not extend to or cover this software or related documentation.

If you are a GE employee or a customer who has entered into such a license agreement with GE to use this proprietary software, you are authorized to use this Material according to the conditions stated in your license agreement.

However, you do not have the permission of GE to alter, decompose or reverse-assemble the software, and unless you are a GE employee, you may not copy the Material. The Material is protected by Copyright and Trade Secret laws; the violation of which can result in civil damages and criminal prosecution.

If you are not party to such a license agreement or a GE Employee, you must exit this Material now.

Trademarks

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

Copyrights

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Translation policy - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-2 Damage in transportation - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-11 Certified electrical contractor statement - For USA Only - - - - - - - - - - - - i-11 Omission and errors - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-12 Service Safety Considerations - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-13 Legal notes - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-14 Proprietary to GE - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-14 Trademarks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-14 Copyrights - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-14

Table of Contents Chapter 1 — Introduction

Overview

Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-2

Manual Overview

Contents in This Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-3 Contents in this service manual - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-3 Typical users of the Basic Service Manual - - - - - - - - - - - - - - - - - - - - - 1-4 LOGIQ e models covered by this manual - - - - - - - - - - - - - - - - - - - - - - 1-5 General Caution - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-6

Important conventions

Conventions used in book - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-7 Standard hazard icons - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-9

Product icons

Label Icon Description - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-11

Safety considerations

Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-19 Contents in this Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-19 Human Safety - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-19 Mechanical safety - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-22 Electrical safety - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-24 Battery Safety- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-26

Dangerous procedure warnings Lockout/Tagout (LOTO) requirements Returning probes and repair parts EMC, EMI and ESD

Contents in this Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-31 What is EMC? - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-31 CE Compliance - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-31 Electrostatic discharge (ESD) prevention - - - - - - - - - - - - - - - - - - - - - 1-32

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Customer assistance

Contact information - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-33 Phone numbers for Customer Assistance - - - - - - - - - - - - - - - - - - - - - 1-34 System manufacturer - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-34 Factory Site - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-35

Chapter 2 — Site Preparations

Overview

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

General 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

Facility needs

Purchaser responsibilities - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-12 Required facility needs - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-13 Desirable features- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-14 Suggested and Alternate Ultrasound Room Layout - - - - - - - - - - - - - - 2-15 Networking setup requirements - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-16

Environmental Dangers

Patient Environment IEC60601-1and ANSI AAMI ES60601-1 - - - - - - - 2-19

Chapter 3 — System Setup

Overview

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

Setup reminders

Contents in this Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-3 Average setup time - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-3 Setup warnings- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-3

Receiving and unpacking the equipment

Contents in this Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-6 Receiving the LOGIQ e - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-6 Unpacking the LOGIQ e - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-7 Packing the Equipment - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-10

Preparing for setup

Verify customer order - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-11 Physical inspection - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-11 EMI protection - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-11

Completing the setup

Contents in this Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-12 System specifications - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-12 Electrical specifications - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-13 Power On / Boot Up - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-14 Power Off/Shutdown - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-16 Connecting probes - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-17

System Configuration

Contents in this Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-19

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LOGIQ e configuration - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-20 Connecting Cables - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-22 Peripheral/Accessories Connector Panel - - - - - - - - - - - - - - - - - - - - - 3-23 Available probes - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-30 Software Options configuration - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-31 Connectivity setup - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-31

Paperwork after setup

User’s Manual(s) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-33 Product Locator Installation Card - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-33

Peripherals Installation

Contents in this Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-34 Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-35 Furnished materials - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-36 Peripherals Installation Instructions - - - - - - - - - - - - - - - - - - - - - - - - - 3-38

Chapter 4 — General Procedures and Functional Checks

Overview

Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-2 Special Equipment required - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-2

General procedures

Contents in this Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-3 Caution and Warning - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-4 Power ON/Boot Up - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-5 Power shut down - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-11 Removable media - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-13 Archiving and loading presets - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-13 Where are the User Manuals and the Service Manual? - - - - - - - - - - - 4-14 How to display or print the PDF files from the Manual CD-ROM? - - - - 4-15 Lockout/Tagout (LOTO) requirements- - - - - - - - - - - - - - - - - - - - - - - - 4-16

Functional checks

Contents in this Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-17 Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-18 Operator Panel - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-18 Soft Menu Key Tour - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-19 Monitor Display- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-20 Performance Tests - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-21 Software Configuration Checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-52 Peripheral Checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-52

Chapter 5 — Components and Functions (Theory)

Overview

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

Block Diagram and Theory

Contents in this Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-3 Block Diagram - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-3 General Information - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-4 Top Console- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-4

Power Diagram

Contents in this Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-5

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Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-5 AC Power - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-5 Battery Charging- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-6 Air Flow Distribution - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-6

Common Service Platform

Contents in this Chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-7 Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-7 The usage for security cable - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-8 Global Service User Interface (GSUI) - - - - - - - - - - - - - - - - - - - - - - - - - 5-9 Service Login - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-9 Access/Security - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-10 Customer Service Home Page - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-13

Chapter 6 — Service Adjustments

LCD Monitor adjustments

Purpose of this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-2 Monitor Adjustments - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-2

Chapter 7 — Diagnostics/Troubleshooting

Overview

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

Gathering Trouble Data

Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-3 Contents in this Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-3 Collect Vital System Information - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-3 Collect a Trouble Image with Logs - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-5

USB Quick Save

Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-7 Check and Record the P3 Key Function - - - - - - - - - - - - - - - - - - - - - - - 7-7 Setting the P3 Key to USB Quick Save - - - - - - - - - - - - - - - - - - - - - - - - 7-8

Screen Capture

Contents in this Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-9 Check and Record the P1 Key Function - - - - - - - - - - - - - - - - - - - - - - 7-10 Setting the P1 Key to Screen Capture- - - - - - - - - - - - - - - - - - - - - - - - 7-10 Capturing a Screen - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-11 Reset the P1 Key to Customer’s Functionality - - - - - - - - - - - - - - - - - - 7-12

Global Service User Interface (GSUI)

Contents in This Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-13 Common Diagnostics - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-13

Network Configuration

Contents in This Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-17 Network Configuration - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-17 Software Download - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-20

Chapter 8 — Replacement Procedures

Overview

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

Warnings and important information

Warnings - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-3 Returning/shipping probes and repair parts - - - - - - - - - - - - - - - - - - - - - 8-4

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Disassembly/Re-assembly

Warning and Caution - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-5 Handle Assy (Part No. 5483188) - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-6

Loading the software

Contents in This Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-13 Purpose of this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-13 Customer provided prerequisite - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-13 Data Management - moving all images - - - - - - - - - - - - - - - - - - - - - - - 8-14 Backing up the Patient Archive and System Configurations - - - - - - - - 8-14 Recording important settings and parameters - - - - - - - - - - - - - - - - - - 8-15 Loading the System Software - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-16

Chapter 9 — Renewal Parts

Overview

Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-2 List of Abbreviations - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-2

Renewal Parts Lists

Contents in This Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-3 Power Cable - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-4 Operator Console Assy - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-5 LCD Assy- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-6 Keyboard Assy - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-7 Bottom Assy- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-9 E-Isolation Cart and Advanced Isolation Cart- - - - - - - - - - - - - - - - - - - 9-13 Accessories and Kits - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-17 Probe - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-19 Manuals- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-21

Chapter 10 — Care and Maintenance

Overview

Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-2

Protecting Health Information

Hide Patient Data - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-3 Protecting Health Information- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-4 Users- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-5 Logon - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-7

Warnings Why do maintenance

Periodic maintenance inspections - - - - - - - - - - - - - - - - - - - - - - - - - - 10-9 Keeping records - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-9 Quality assurance - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-10

Maintenance task schedule

How often should maintenance tasks be performed? - - - - - - - - - - - - 10-11

Tools required

Standard GE tool kit - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-13 GE-2 tool kit - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-15 Special tools, supplies and equipment used for maintenance - - - - - - 10-16

System maintenance

Contents in This Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-17

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Preliminary checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-17 Functional checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-19 Physical inspection - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-21 Optional Diagnostic Checks- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-22 Probe maintenance - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-23 Battery Performance Maintenance - - - - - - - - - - - - - - - - - - - - - - - - - 10-25

Electrical safety tests

Contents in This Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-26 Safety test overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-26 Leakage current limits - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-29 Outlet test - wiring arrangement - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-31 Grounding continuity - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-32 Chassis leakage current test - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-33 Probe leakage current test- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-35

When there's too much leakage current …

AC/DC Fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-38 Chassis Fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-38 Probe Fails- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-39 Peripheral Fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-39 Still Fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-39 New Unit - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-39 ECG Fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-39

Inspection Paperwork

Ultrasound Inspection Forms - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-40

Electrical Safety Tests Log

Chapter 11 — Docking Cart Setup

Overview

Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-2

Set Up Docking Cart

Contents in This Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-4 Setup Reminders - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-5 Receiving and Unpacking the Equipment - - - - - - - - - - - - - - - - - - - - - 11-8 Preparing for Installation - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-12 Peripheral Installation - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-14 Options Installation - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-24 Paperwork - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-38

Cart Using

Contents in This Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-39 Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-39 Height Adjustment - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-39 Locking the Wheels- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-40 Mounting the System to Cart - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-40 Release the System from Docking Cart- - - - - - - - - - - - - - - - - - - - - - 11-41 Switch the Three Probes - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-42 System Operation - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-42

Docking Cart Functions (Theory)

Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-43

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Block Diagram - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-43 Information- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-44 Supported External Interface/Port- - - - - - - - - - - - - - - - - - - - - - - - - - 11-44 Configuration on External Display Through DVI Connection - - - - - - - 11-45

Diagnostics/Troubleshooting

Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-51 Troubleshooting - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-51 Gathering Trouble Data - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-51 Troubleshooting Trees - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 11-52

Chapter 12 — Docking Cart Servicing

Overview

Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-2 List of Abbreviations - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-2

Replacement Procedure

Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-3 Contents in this Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-3 Disassembly/Re-assembly- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-3

Renewal Parts

Contents in This Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-12 Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-12 Power Cable - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-13 Operator Console Assy - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-14 Docking Station - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-15 Probe Holder - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-17 Shelf Service - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-19 Bottom and Wheels- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-20 Panel and Cabinet - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-21 Gas Spring and Gas Spring Lever - - - - - - - - - - - - - - - - - - - - - - - - - 12-21 Power Box and Extended Life Battery- - - - - - - - - - - - - - - - - - - - - - - 12-21

Care & Maintenance

Contents in This Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-23 Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-23 Why do Maintenance - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-25 Maintenance Task Schedule - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-26 Tools Required - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-28 Cleaning Dusk Screen- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-29 Safety Test- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-30 Safety Test (continued) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-33 When There’s Too Much Leakage Current... - - - - - - - - - - - - - - - - - - 12-34 Inspection Paper Work - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 12-35

Index

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Chapter 1

Introduction

This chapter describes important issues related to safely servicing the Ultrasound system and Docking Cart. The service provider must read and understand all the information presented here before installing or servicing the units.

LOGIQ e – Basic Service Manual 1-1 5461614-100 English Rev. 6

Introduction

Contents in this chapter

• ‘Overview’ on page 1-2

• ‘Manual Overview’ on page 1-3

• ‘Important conventions’ on page 1-7

• ‘Product icons’ on page 1-11

• ‘Safety considerations’ on page 1-19

• ‘Dangerous procedure warnings’ on page 1-28

• ‘Lockout/Tagout (LOTO) requirements’ on page 1-29

• ‘Returning probes and repair parts’ on page 1-30

• ‘EMC, EMI and ESD’ on page 1-31

• ‘Customer assistance’ on page 1-33

Overview

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This manual provides installation and service information for the LOGIQ e Ultrasound system and docking cart. It is divided in twelve chapters as shown below.

Contents in This Section

• ‘Contents in this service manual’ on page 1-3

• ‘Typical users of the Basic Service Manual’ on page 1-4

• ‘LOGIQ e models covered by this manual’ on page 1-5

• ‘General Caution’ on page 1-6

Contents in this service manual

Manual Overview

Chapter number

The manual is divided into twelve 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).

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 e and Docking Cart.

‘System Setup’ Contains setup procedure with procedure

checklist for the system.

‘General Procedures and Functional Checks’

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

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Introduction

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

Chapter number

10.

11.

12.

Chapter title Description

‘Components and Functions (Theory)’

‘Service Adjustments’

‘Diagnostics/ Troubleshooting’

‘Replacement Procedures’

Contains block diagrams and functional explanations of the electronics for the system.

Contains instructions on how to make any available adjustments to the LOGIQ e system.

Provides procedures for running diagnostic or related routines for the LOGIQ e system.

Provides disassembly procedures and reassembly procedures for all changeable FRU on the system.

‘Renewal Parts’ Contains a complete list of replacement parts for

LOGIQ e system.

‘Care and Maintenance’

Provides periodic maintenance procedures for LOGIQ e system.

‘Docking Cart Setup’ Provides setup information for Docking Cart,

including use, test and trouble shooting of Docking Cart.

Provides service information for Docking Cart,

‘Docking Cart Servicing’

including replacement, spare parts and Maintenance.

N/A Index A quick way to the topic you’re looking for.

Typical users of the Basic Service Manual

• Service personnel (installation, maintenance, etc.)

• Hospital’s service personnel

• Contractors (some parts of Chapter 2 - Pre-Installation)

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LOGIQ e models covered by this manual

Table 1-2: LOGIQ e Model Designations

Model Number Description

5483518 LOGIQ e Console for USA

5483522 LOGIQ e Console

5498957 LOGIQ e Console for CKD

5499582 LOGIQ e Console for Canada

5483520 LOGIQ e Console for Korea

5483521 LOGIQ e Console for China

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

applies to all LOGIQ e models.

Purpose of the operator manual(s)

Manual Overview

The operator manuals should be fully read and understood before operating the LOGIQ e and also kept near the unit for quick reference.

The online versions of the operator manuals are available via the Help function on LOGIQ e’s operator panel.

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Introduction

General Caution

CAUTION

Standard maintenance must be performed by authorized service personnel for the lifetime of the product (7 years).

Proceed cautiously when crossing door or elevator thresholds with the Docking Cart or Isolation Cart. Use the handle to push/ pull the system, e.g., do not use the Docking Cart external LCD. Failure to do so may cause serious injury or system damage.

Capacity load of the Docking Cart: The maximum capacity load of the Storage rack (1) is 2kg, DVD-RW Shelf (2) is 2kg, B/W Printer Shelf (3) is 4kg, Color Printer Shelf (4) is 7kg, refer to the following figure.

Figure 1-1. Capacity load of the Docking Cart

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Conventions used in book

Important conventions, used in this document, are described next.

Model designations

This manual covers the LOGIQ e Ultrasound systems listed in:

‘LOGIQ e 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.

Important conventions

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Introduction

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

WARNING

CAUTION

NOTE: Notes are used to provide important information about an item

NOTE: Be sure to read the notes; the information contained in a note

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.

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.

or a procedure.

can often save you time or effort.

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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.

Important conventions

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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Introduction

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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The following table describes the purpose and location of safety

ＲＥＦ

ＳＮ

labels and other important information provided on the equipment.

Label Icon Description

The following table describes the purpose and location of safety labels and other important information provided on the equipment.

Label/Icon Purpose/Meaning Location

Product icons

Table 1-5: Product Icons

Identification and Rating Plate • Manufacture’s name and

address

• Date of manufacture

• Model and serial numbers

• Electrical ratings (Volts, Amps, phase, and frequency)

Date of manufacture: The date could be a year, year and month, or year, month and day, as appropriate. See ISO 8601 for date formats.

Catalog or model number Bottom

ＲＥＦ

Serial number Bottom

ＳＮ

Direct Current: For products to be powered from a DC supply

Rating plate

Bottom

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Introduction

Table 1-5: Product Icons (Continued)

Label/Icon Purpose/Meaning Location

Input Bottom

For use with adapter GE part number 5460229-x

Description Bottom

Model Rear of Docking Cart

Only for use with LOGIQ e series (Software version R8.x.x)

Made in China Rear of Docking Cart

Type/Class Label Used to indicate the degree of

safety or protection.

IP Code (IPX8) IPX8: MKF 2-MED GP26

Indicates the degree of protection provided by the enclosure per IEC60 529. IPX8 can be used in an operating room environment.

Bottom

Rear of Docking Cart

Bottom of Footswitch

Authorized European Representative address.

United States only Prescription Requirement label.

Type BF Applied Part (man in the box) symbol is in accordance with IEC 878-02-03.

Bottom panel

Beside the probe connector

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Product icons

Table 1-5: Product Icons (Continued)

Label/Icon Purpose/Meaning Location

General Warning. Various

“CAUTION” - Dangerous voltage” (the lightning flash with arrowhead) is used to indicate electric shock hazards.

“ON” indicates the power on position of the power switch.

CAUTION: This Power Switch DOES NOT ISOLATE Mains

Supply.

“Protective Earth” indicates the protective earth (grounding) terminal.

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

Type CF Defib-Proof Applied Part (heart in the box with paddle) symbol is in accordance with IEC 60878-02-06.

Various

See the Console Overview section for location information.

Inside of AC adapter

Bottom

ECG Module

“Consult accompanying documents“ is intended to alert the user to refer to the operator manual or other instructions when complete information cannot be provided on the label.

Do not push the system. Rear of Docking Cart/

Various

Isolation Cart

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Introduction

Table 1-5: Product Icons (Continued)

Label/Icon Purpose/Meaning Location

This symbol indicates that waste electrical and electronic equipment must not be disposed of as unsorted municipal waste and must be collected separately. Please contact an authorized representative of the manufacturer for information concerning the decommissioning of your equipment.

The separate collection symbol is affixed to a battery, or its packaging, to advise you that the battery must be recycled or disposed of in accordance with local or country laws. The letters below the separate collection symbol indicate whether certain elements (Pb=Lead,Cd=Cadmium, Hg=Mercury) are contained in the battery. To minimize potential effects on the environment and human health, it is important that all marked batteries that you remove from the product are properly recycled or disposed. For information on how the battery may be safely removed from the device, please consult the service manual or equipment instructions. Information on the potential effects on the environment and human health of the substances used in batteries is available at this url: http://www.gehealthcare.com/ euen/weee-recycling/index.html

Bottom

Battery Pack if contains Pb/Cd/Hg

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Product icons

Table 1-5: Product Icons (Continued)

Label/Icon Purpose/Meaning Location

No hazardous substance, above the maximum concentration value, is present. Maximum concentration values for electronic information products, as set by the People’s Republic of China Electronic Industry Standard SJ/T11364-2006, include the hazardous substances of lead, mercury, hexavalent chromium, cadmium, polybrominated biphenyl (PBB), and polybrominated diphenyl ether (PBDE).

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

Probe and Rear Panel, China Rating Plate

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Introduction

Table 1-5: Product Icons (Continued)

Label/Icon Purpose/Meaning Location

Indicates the presence of hazardous substance(s) above the maximum concentration value. Maximum concentration values for electronic information products, as set by the People’s Republic of China Electronic Industry Standard SJ/ T11364-2006, include the hazardous substances of lead, mercury, hexavalent chromium, cadmium, polybrominated biphenyl (PBB), and polybrominated diphenyl ether (PBDE). “20” indicates the number of years during which the hazardous substance(s) will not leak or mutate so that the use of this product will not result in any severe environmental pollution, bodily injury, or damage to any assets.

When closing the LCD cover, use caution to avoid injuring hands or fingers as there is a closing mechanism which allows the LCD cover to automatically close.

Rating Plate

Bottom

Do not connect the DVD-RW to the system while scanning. The DVD-RW can be used when connecting to the Docking Cart.

GOST symbol: Russia Regulatory Country Clearance.

This product consists of devices that may contain mercury, which must be recycled or disposed of in accordance with local, state, or country laws. (Within this system, the backlight lamps in the monitor display, contain mercury.)

DVD-RW

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

Bottom

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Product icons

Table 1-5: Product Icons (Continued)

Label/Icon Purpose/Meaning Location

INMETRO Certification: TUV Rheinland Brazil

Disconnect the probe connector of Three-Probe Port before remove the system from Docking Cart Platform, otherwise the probe cable will be damaged.

Guidance on how to connect the system to the docking cart and how to release it. When put the system on docking cart top cover, avoid injuring the fingers and hands. Make sure the system’s handle is locked well after mounting the system to docking cart top cover. When connecting the probe connector to the system, press the probe connector locking lever up. When releasing the system from the docking cart, disconnect the probe connector of Three-Probe Port from the system before lifting up the system.

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

Docking Cart Top Cover

Do not disconnect the probe connector of Three-probe Port from the system when the system is in use.

Probe Connector of Three-Probe Port

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Introduction

Table 1-5: Product Icons (Continued)

Label/Icon Purpose/Meaning Location

Do not let the 3-Probe Port drop down when mounting it to the docking cart. The 3-Probe Port will be damaged if it drops on hard surface.

When pushing the Extended Life Battery in to the power box, use caution to avoid injuring fingers and hands.

3-Probe Port

Power Box

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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.

Contents in this Section

• ‘Human Safety’ on page 1-19

• ‘Mechanical safety’ on page 1-22

• ‘Electrical safety’ on page 1-24

• ‘Battery Safety’ on page 1-26

Safety considerations

Human Safety

DANGER

WARNING

• Operating personnel must not remove the system covers.

• Servicing should be performed by authorized personnel only.

Only personnel who have participated in a LOGIQ e 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 e, 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

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.

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)

Safety considerations

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.

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Introduction

Mechanical safety

WARNING

CAUTION

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.

LOGIQ e system weighs 5.2 kg or more, depending on installed peripherals, when ready for use. Care must be used when moving it or replacing its parts.

ALWAYS:

• 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)

Safety considerations

CAUTION

WARNING

CAUTION

The Docking Cart weighs 53 kg (117 lb.) or more, depending on installed peripherals, when ready for use. Care must be used when moving it or replacing its parts.

Failure to follow the precautions listed below could result in injury, uncontrolled motion and costly damage.

ALWAYS:

• be sure the pathway is clear

• use slow, careful motions

• Limit movement to a slow careful walk.

• use two people when moving on inclines or lifting more than 16 kg (35 lbs)

When the docking cart is raised for a repair or moved along any incline, use external caution since it may become unstable and tip over.

Make sure the console be fixed well to avoid the console falling down when moving Docking Cart.

CAUTION

Do not move Docking Cart with big incline angle.

The Docking Cart is not water proof. Do not expose the Docking Cart to water or any kind of liquid.

Never set liquids on the Docking Cart to ensure that liquid does not drip into the unit

CAUTION

Put peripherals in correct position to avoid Docking Cart overload.

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Introduction

Mechanical safety (continued)

NOTE: Special care should be taken when transporting the Docking

Cart in a vehicle.

• Secure the unit in an upright position.

• Lock the wheels (brake)

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

1-24 LOGIQ e – Basic Service Manual

Connecting a LOGIQ e 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

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 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 e, please make sure the battery is removed.

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Battery Safety (continued)

Safety considerations

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.

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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

WARNING

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 e, 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.

WARNING

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

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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.

WARNING

All potentially hazardous stored or residual energy is relieved.

Energy Control and Power Lockout for LOGIQ e.

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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Contents in this Section

• ‘What is EMC?’ on page 1-31

• ‘CE Compliance’ on page 1-31

• ‘Electrostatic discharge (ESD) prevention’ on page 1-32

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.

EMC, EMI and ESD

CE Compliance

LOGIQ e 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’s 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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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.

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

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, 4D multi-volume loop.

NOTE: Restart the application before resuming clinical scanning.

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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 & Primary Care Diagnostics, LLC 9900 Innovation Drive Wauwatosa, WI 53226

Canada 1-800-668-0732

Latin America Service

Europe GE Ultraschall Deutschland Gmbh & Co. KG Beethovenstrasse 239 Postfach 11 05 60, D-42655 Solingen Germany

Asia (Singapore) GE Ultrasound Asia Service Department - Ultrasound 298 Tiong Bahru Road #15-01/06 Central Placa Singapore 168730

Japan Support Center 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

Phone: +33 (0) 130-831-300

Fax: +49 (0) 2122-8024-31

Tel: +65 6291-8528

Fax: +65-6291-7006

Fax:

1-262-524-5300 1-262-524-5698

(General Imaging and Cardiac) +49 (0) 212-2802-652

81-426-48-2940 81-426-48-2905

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

+86 510 85225888 +86 510 85226688

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Factory Site

MANUFACTURER PHONE NUMBER FAX NUMBER

Customer assistance

Table 1-8: System manufacturer

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

+86 510 85225888 +86 510 85226688

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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 and Docking Cart. Included are descriptions of the facility and electrical needs to be met by the purchaser of the units.

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Site Preparations

Contents in this chapter

• ‘Overview’ on page 2-2

• ‘General requirements’ on page 2-3

• ‘Facility needs’ on page 2-12

• ‘Environmental Dangers’ on page 2-19

Overview

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General requirements

Contents in this Section

• ‘Ultrasound system environmental requirements’ on

page 2-3

• ‘Electrical requirements’ on page 2-6

• ‘Electrical requirements for Docking Cart’ on page 2-8

• ‘EMI limitations’ on page 2-9

• ‘EMI prevention/abatement’ on page 2-10

• ‘Probes environmental requirements’ on page 2-11

Ultrasound system environmental requirements

General 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

Degree C 50 45 40 35 30 25 20 15 10 5 0 -5

Degree F 122113104958677685950413223

hours 420000000246

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

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Site Preparations

Environmental specifications

The system and Docking Cart 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

(with probe)

Temperature 10 - 40°C

50 - 104°F

Humidity 30 - 75%

non-condensing

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

Storage

LOGIQ e

-5 - 50°C 23 - 122°F

10 - 90% non-condensing

Trans port

LOGIQ e

-5 - 50°C 23 - 122°F

10 - 90% non-condensing

Table 2-3: Environmental Requirements for Docking Cart

Operation Storage Transpo rt

Temperature 10 - 40°C

50 - 104°F

Humidity 30 - 75%

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

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General requirements

Environmental specifications (continued)

Table 2-4: Environmental Requirements for an Ultrasound Room for Docking Cart

Item Val ues

Power Source Refer to Table 2-6 on page 2-8.

Power Rating 500VA (100V-120V); 500VA (220-240V)

Radiation Shielding NONE REQUIRED for ULTRASOUND ENERGY

Floor Landing

Floor Condition Gradient: WITHIN 5 degrees

Weight 53 kg without Accessories

Approximately 680 - 800 kg/m

NOTE: Temperature in degrees Celsius (ºC) conversion to

degrees F (ºF): (ºF) = (ºC * 9/5) + 32

without Accessories

CAUTION

Lighting

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

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

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 Adapter

Table 2-5: Electrical Specifications for Adapter

Adapter Model

Input Voltage

Input Current

Output Power

AHM150PS19-XA1048

100-240VAC

1.5A at 115VAC

0.75A at 230VAC

150W

Output Voltage

Output Current

Frequency

19.0VDC

7.89A

50/60Hz

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Site circuit breaker

General requirements

CAUTION

Site power outlets

Power outage may occur. The LOGIQ e 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 e 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.

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.

Power stability requirements

Voltage drop-out:

Max 10 ms.

Power transients:

Less than 25% of nominal peak voltage for less than 1 millisecond for any type of transient, including line frequency, synchronous, asynchronous, or aperiodic transients.

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Site Preparations

Electrical requirements for Docking Cart

Table 2-6: Electrical requirements for Docking Cart

PARAMETER AREA LIMITS

Voltage Range 100-240V~ 350VA

Power All applications More than or equal to 750 VA

Line Frequency All applications 50/60Hz (±2Hz)

Power Transients All applications Less than 25% of nominal peak voltage for less

than 1 millisecond for any type of transient, including line frequency, synchronous, asynchronous, or aperiodic transients.

Decaying Oscillation All applications Less than 15% of peak voltage for less than 1

millisecond.

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EMI limitations

General 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 2-7: 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 requirements

Probes environmental requirements

Operation and storage temperatures for probes

Table 2-8: Operation and storage temperatures for probes

Conditions Temp eratu re

Operation: 10 to 40 ºC (50 to 104 ºF)

Storage: -5 to 50 ºC (23 to 122 ºF)

Temperature in degrees Celsius (ºC) conversion to degrees F (ºF):

(ºF) = (ºC * 9/5) + 32

NOTE: SYSTEMS AND ELECTRONIC PROBES ARE DESIGNED

FOR STORAGE TEMPERATURES OF -5 TO + 50 degrees C. WHEN EXPOSED TO LARGE TEMPERATURE VARIATIONS, THE PRODUCT SHOULD BE KEPT IN ROOM TEMPERATURE FOR 10 HOURS BEFORE USE.

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Site Preparations

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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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.

Facility needs

Sites with a mains power system with defined Neutral and Live

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

Sites with a mains power system without a defined Neutral

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

NOTE: Please note that image artifacts can occur, if at any time within

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

• 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 0.2m (0.67 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 and gel warmer

• Power outlets for test equipment and modem within 1 m (3.2 ft.) of unit

• Clean and protected space to store transducers (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.

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Site Preparations

Desirable features

• Door is at least 92 cm (3 ft.) wide

• Circuit breaker for dedicated power outlet is easily accessible

• Sink with hot and cold water

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

• Emergency oxygen supply

• Storage for linens and equipment

• Nearby waiting room, lavatory, and dressing room

• Dual level lighting (bright and dim)

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

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Suggested and Alternate Ultrasound Room Layout

Recommended standard floor plan and a minimal floor plan for ultrasound equipment:

Facility needs

F IL M VIE WE R

F IL M SUPPLIES

FILM

F ILE

C AB INE T

SE CR E TA R YS OR DO C TO R 'S D ES K

SIN K

DEDIC ATE D

POWER

R OOM ,

PR O C ESSIN G

F IL M VIE W ER

C OUN T E R TO P

RECEP TACLE

C OUN T E R

TO P

SIN K

SU C T IO N LINE

EMERGECY OX Y G EN

O VE RH E AD LI G HT S D IMME R

DOOR

42 IN .

(107 C M)

C ONS O LE

F OOT

A 14 by 17 foot R ecommended Floor P lan

S cale : E ach square equals one square foot

LINEN SUPPLY

PR OB ES /SUPPLIES

S TOO L

(193 C M)

18 IN .

(46 CM)

76 IN .

LINEN SUPPLY

E XAM IN AT ION

TAB LE

24 IN .

(61 CM)

PAT IEN T

TO ILE T

F AC ILI T Y

EXT ERNAL

DOOR 30 IN .

(76 CM)

24 IN . (61 CM)

FOOT

STOOL

E XAM IN AR IO N

TAB LE

PE R IP HE R ALS

LOGIQ Book XP

CONSOLE

76 IN . (193 C M)

DEDIC ATED POWER OUTLET S

G E C AB INE T FOT S OFTWARE A ND MANU ALS

A n 8 by 10 foot Minimal Floor P lan

Figure 2-1. Suggested Ultrasound Room Layout

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Site Preparations

Networking setup requirements

Stand alone Ultrasound system (without network connection)

None.

Scanner connected to hospital’s network

Supported networks:

Wireless LAN

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.

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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 in ”Figure 2-2 on page 2-18. Ensure that there are no spaces in any field of the form.

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.

Facility needs

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Site Preparations

DICOM option setup requirements (continued)

Figure 2-2. Worksheet for DICOM Network Information

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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 UL60601-1 and IEC60601-1 / IEC60601-1-1 standards for electrical leakage.

Patient Environment IEC60601-1and 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 2-3. Patient environment

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Site Preparations

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Chapter 3

System Setup

This chapter contains information needed to install LOGIQ e 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 3-11

• ‘Completing the setup’ on page 3-12

• ‘System Configuration’ on page 3-19

• ‘Connectivity setup’ on page 3-31

• ‘Paperwork after setup’ on page 3-33

• ‘Peripherals Installation Instructions’ on page 3-38

Overview

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Contents in this Section

• ‘Average setup time’ on page 3-3

• ‘Setup warnings’ on page 3-3

Average setup time

• Unpacking the LOGIQ e: 20 minutes

• Set up LOGIQ e wo/options: 30 minutes

• DICOM Network Configuration: 30 minutes

The LOGIQ e installation and functional checkout will take approximately one hour. LOGIQ e consoles with optional equipment may take slightly longer.

Setup reminders

Setup warnings

DANGER

CAUTION

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.

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System Setup

Setup warnings (continued)

CAUTION

NOTE: For information regarding packing labels, refer to LABELS

DANGER

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.

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.

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 10×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.

CAUTION

3-4 LOGIQ e – Basic Service Manual

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.

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Setup warnings (continued)

Setup reminders

DANGER

CAUTION

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 UNIT!

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 operate this unit unless all board covers are securely in place.

Operator Manual(s)

The User Manual(s) should be fully read and understood before operating the LOGIQ e and kept near the Ultrasound system for quick reference.

Acoustic Output Hazard

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

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System Setup

Receiving and unpacking the

Contents in this Section

• ‘Receiving the LOGIQ e’ on page 3-6

• ‘Unpacking the LOGIQ e’ on page 3-7

• ‘Moving into Position’ on page 3-10

Receiving the LOGIQ e

Overview

equipment

Examine all packages

Improper handling during transportation may harm the equipment inside the package even if the package itself is undamaged.

Examine package closely at time of delivery, as described in the procedure below.

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Unpacking the LOGIQ e

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

1. Cut the four PLASTIC BANDs

2. Cut the adhesive tape and open top covers of paper carton.

Receiving and unpacking the equipment

Adhesive tape

Plastic Bands

Figure 3-1. Open Top Covers of Paper Carton

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System Setup

Unpacking the LOGIQ e (continued)

3. Take out the Paper pad.

4. Take out console together with 2 interleavers from console package.

5. Take out the interleavers beside Accessories Package

6. Take out Accessories Package.

Paper Pad

Console and interleavers

Console Package

CAUTION

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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Receiving and unpacking the equipment

Unpacking the LOGIQ e (continued)

7. Remove 2 interleavers.

8. Remove plastic bag.

Interleaver

Console

Figure 3-3. Removing interleavers and plastic bag

Interleaver

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System Setup

Unpacking the LOGIQ e (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

CAUTION

Please carefully unpack the system, and do not dispose the package of LOGIQ e, so that it can be reused for service.

Moving into Position

CAUTION

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 e. 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 e in the reverse order of unpacking.

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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

System Voltage Settings

Verify that the system arrived intact (visual inspection).

If the system has been damaged, please refer to ‘Damage in

transportation’ on page i-11 in the beginning of this manual.

Preparing for setup

WARNING

EMI protection

• Verify that the scanner is set to the correct voltage. The Voltage settings for the LOGIQ e Scanner is found on a label located on the AC adapter.

• 220-240VAC(China); 100-120VAC(USA/Japan); 220-240VAC(Europe, Latin America).

Connecting a LOGIQ e system to the wrong voltage level will most likely destroy the scanner.

The LOGIQ e 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

Completing the setup

Contents in this Section

• ‘System specifications’ on page 3-12

• ‘Electrical specifications’ on page 3-13

• ‘Power On / Boot Up’ on page 3-14

• ‘Power Off/Shutdown’ on page 3-16

• ‘Connecting probes’ on page 3-17

System specifications

System requirements verification

Physical dimensions

Console Weight

• 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.

The physical dimensions vary from product to product. You may copy and use the table below in your local manuals or local core content.

• Height: 70 mm (2.75 in) console only; 100 mm (3.94 in) with handle

• Length: 346 mm (13.62 in) console only; 375 mm (14.76 in) with handle

• Width: 295 mm (11.61 in) console only; 343 mm (13.50 in) with handle

• Weight (with battery): approx. 5.2 kg (11.5 lbs)

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Electrical specifications

Completing the setup

WARNING

Connecting a LOGIQ e 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 e is available on-site.

Electrical specifications for LOGIQ e

Figure 3-5. AC Adapter label

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System Setup

ＵＰ

Power On / Boot Up

NOTE: After turning off a system, wait at least ten seconds before

System Power On

turning it on again. The system may not be able to boot if power is recycled too quickly.

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

ＵＰ

Figure 3-6. Connect AC adapter

When power is applied to the system, power is distributed to the Cooling Unit, Control Panel, LCD, Peripherals and the Back-end Processor.

CAUTION

The system should rest on the handle to allow an air gap to prevent overheating.

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Power on the system

Completing the setup

Press the Power On/Off switch at the front of the system once.

Figure 3-7. Power On/Off Switch

When the Power On/Off switch on the Control Panel is pressed once, the Back-end Processor starts and the software code is distributed to initiate the scanner.

No status messages are displayed during this process.

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System Setup

Power Off/Shutdown

NOTE: After turning off a system, wait at least ten seconds before

turning it on again. The system may not be able to boot if power is recycled too quickly.

Back-end Processor Power off

To power off the system:

1. Press the Power On/Off switch at the front of the system once.

2. The system-Exit window is displayed.

Figure 3-8. System Exit Window

3. Using the Trackball or Select key, select Shutdown.

4. The shutdown process takes a few seconds and is complete when the power status LED is turned off.

5. Disconnect the probes.Clean or disinfect all probes as necessary. Store them in their shipping cases to avoid damage.

6. Close LCD cover.

System Shutdown

Disconnect the Mains Power Cable if necessary. For example: Relocating the system.

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Connecting probes

Connect a probe

NOTE: It is not necessary to turn OFF power to connect or disconnect a

Completing the setup

probe.

CAUTION

NOTE: Please ensure that the probe latch is in an unlocked position

Do not allow the probe head to hang freely. Excessive impact to the probe will result in irreparable damage.

To prevent probe connector pins damage, or PCB board damage, do not use excessive force when connecting the probes.

Keep the probe cables away from the wheels.

Do not bend the probe cables.

Do not cross cables between probes.

Follow these steps to connect a probe:

Probes can be connected at any time, whether the unit is On or Off.

Carefully open the system LCD display, plug the probe connector into the probe port, then lock the probe latch upward.

before you connect the probe to the system.

1. Before connecting the probe:

a. Do a visual check of the probe pins and system sockets.

b. Remove any dust or foam rests from the probe pins.

c. Verify the probe and the probe cable for any visual

damage.

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System Setup

Connect a probe (continued)

2. Position the probe cable so that it is not resting on the floor.

Probe Latch

Figure 3-9. Probe connectors

Disconnect a probe

Follow these steps to disconnect a probe:

1. Remove the connector from the port.

2. Ensure that the probe head is clean before placing the probe in its storage case.

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Contents in this Section

• ‘LOGIQ e configuration’ on page 3-20

• ‘Electrical requirements for Adapter’ on page 3-21

• ‘Approved peripherals’ on page 3-21

• ‘Connecting Cables’ on page 3-22

• ‘Peripheral/Accessories Connector Panel’ on page 3-23

• ‘Pin Assignment’ on page 3-24

• ‘Available probes’ on page 3-30

• ‘Software Options configuration’ on page 3-31

System Configuration

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System Setup

LOGIQ e configuration

System Specification

The physical dimensions of the LOGIQ e console with old LCD are summarized as below:

Table 3-1: Physical Dimensions of LOGIQ e

Height Width Depth Unit

Console

Only

70 100 295 343 346 375 mm

2.75 3.94 11.61 13.50 13.62 14.76 inches

with

Handle

Console

Only

Console

with

Handle

Console

Only

Console

with

Handle Unit

Figure 3-10. Overall Dimensions and Weight

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General Electric LOGIQ E R6 BASIC SERVICE MANUAL_SM_5461614-100_6 Technical Publication LOGIQ e Basic Service Manual Direction Number: 5461614-100 English Rev. 6

Specifications and Main Features

Frequently Asked Questions

User Manual

LOGIQ e

Table of Contents

Introduction

Overview

Manual Overview

Important conventions

Product icons

Safety considerations

Dangerous procedure warnings

Lockout/Tagout (LOTO) requirements

Returning probes and repair parts

EMC, EMI and ESD

Customer assistance

Site Preparations

Overview

General requirements

Facility needs

Environmental Dangers

System Setup

Overview

Setup reminders

Preparing for setup

Completing the setup

System Configuration