GE LOGIQ V2, V1 ultrasound system Basic Service Manual
Below you will find brief information for LOGIQ V2, LOGIQ V1. The LOGIQ V2 and LOGIQ V1 ultrasound systems are designed to provide high-quality images for a variety of clinical applications. These systems offer a range of features that can help you make more accurate diagnoses and improve patient care.
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Technical Publication
LOGIQ V2/LOGIQ V1
Basic Service Manual
Direction Number: 5610739-100 English
Rev.3
GE
All Material Copyright © 2015 by General Electric Company Inc.
All Rights Reserved.
Product Information
This Manual covers the software version of R1.x.x for LOGIQ V2, LOGIQ V1 ultrasound system.
GE
Copyright © 2015, General Electric Company.
GE Medical Systems, a General Electric Company, going to market as GE
Manufacturer:
GE Medical Systems (China) Co., Ltd.
No. 19, Changjiang Road
WuXi National Hi-Tech Development Zone
Jiangsu, P.R. China 214028
TEL: +86 510 85225888; FAX: +86 510 85226688 www.gehealthcare.com
Revision history
Rev.1
Revision
Rev.2
Rev.3
Front
Front matter
TOC
Chapter 1
Chapter 2
Chapter 3
Chapter 4
Chapter 5
Pages
Revision History
Date
(YYYY/MM/DD)
2015/06/09
2015/11/13
2015/11/23
Reason for change
Initial Release
New software version, general update
Add software wipe information
List of Effected Pages (LOEP)
Revision
Rev.3
Rev.3
Rev.3
Rev.3
Rev.3
Rev.3
Rev.3
Rev.3
Chapter 6
Chapter 7
Chapter 8
Chapter 9
Chapter 10
Index
Rear Cover
Pages Revision
Rev.3
Rev.3
Rev.3
Rev.3
Rev.3
Rev.3
Rev.3
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
Mail the information to:
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.
GE Medical Systems (China) Co., Ltd.
No. 19 Changiang Road
Wuxi National Hi-Tech Dev. Zone
Jiangsu
P.R.China 214028
GE employees should use TrackWise to report service documentation issues.
These issues will then be in the internal problem reporting tool and communicated to the writer.
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Service Safety Considerations
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
Trademarks
Copyrights
The contents of this publication may not be copied or duplicated in any form, in whole or in part, without prior written permission of GE.
GE may revise this publication from time to time without written notice.
All products and their name brands are trademarks of their respective holders.
All Material Copyright © 2015 by General Electric Company Inc.
All Rights Reserved.
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Table of Contents
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
Trademarks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-14
Copyrights - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-14
Table of Contents
Chapter 1 — Introduction
Overview
Contents in this chapter- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-2
Manual Overview
Contents in this manual - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-3
Typical users of the Proprietary Service Manual - - - - - - - - - - - - - - - - - 1-4
LOGIQ V2/LOGIQ V1 models covered by this manual - - - - - - - - - - - - - 1-5
Important conventions
Conventions used in book - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-6
Standard hazard icons - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-8
Product icons
Labels locations
Safety considerations
Contents in this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-12
Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-12
Human Safety - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-12
Mechanical safety - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-15
Electrical safety - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-17
Battery Safety- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-19
Dangerous procedure warnings
Lockout/Tagout (LOTO) requirements
Returning probes and repair parts
EMC, EMI and ESD
What is EMC? - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-24
CE Compliance - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-24
Electrostatic discharge (ESD) prevention - - - - - - - - - - - - - - - - - - - - - 1-25
Customer assistance
Contact information- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-26
Phone numbers for Customer Assistance - - - - - - - - - - - - - - - - - - - - - 1-27
System manufacturer - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-27
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Authorized Representative- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-28
Chapter 2 — Site Preparations
Overview
Contents in this chapter- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-2
General Ultrasound system requirements
Contents in this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-3
Ultrasound system environmental requirements- - - - - - - - - - - - - - - - - - 2-3
Electrical requirements - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-6
EMI limitations - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-9
Probes environmental requirements - - - - - - - - - - - - - - - - - - - - - - - - - 2-11
Time and manpower requirements - - - - - - - - - - - - - - - - - - - - - - - - - - 2-11
Facility needs
Contents in this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-12
Purchaser responsibilities - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-13
Required facility needs - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-14
Desirable features- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-15
Minimal floor plan suggestion- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-16
Recommended floor plan suggestion - - - - - - - - - - - - - - - - - - - - - - - - 2-17
Suggested floor plan, Ultrasound system, and EchoPAC PC in same room - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-18
Networking setup requirements - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-19
Environmental Dangers
Patient Environment IEC60601-1 and ANSI AAMI ES60601-1 - - - - - - 2-22
Chapter 3 — System Setup
Overview
Contents in this chapter- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-2
Setup reminders
Average setup time - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-3
Setup warnings- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-3
Receiving and unpacking the equipment
Purpose of this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-6
Contents in this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-6
Warnings for receiving and unpacking - - - - - - - - - - - - - - - - - - - - - - - - 3-6
Receiving the LOGIQ V2/LOGIQ V1 - - - - - - - - - - - - - - - - - - - - - - - - - - 3-6
Unpacking the LOGIQ V2/LOGIQ V1 - - - - - - - - - - - - - - - - - - - - - - - - - 3-8
Packing the Equipment - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-11
Packing materials - recycling information
Preparing for setup
Verify customer order - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-13
Physical inspection - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-13
EMI protection - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-13
Completing the setup
Purpose of this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-14
Contents in this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-14
System specifications - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-14
Electrical specifications - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-15
Peripheral/Accessories Connector Panel - - - - - - - - - - - - - - - - - - - - - 3-16 i-16 LOGIQ V2/LOGIQ V1 – Basic Service Manual
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Connecting probes - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-17
Powering the system- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-17
System Configuration
Purpose of this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-18
LOGIQ V2/V1 configuration - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-18
Peripherals Installation
Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-19
Furnished materials - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-20
Peripherals Installation Instructions - - - - - - - - - - - - - - - - - - - - - - - - - 3-22
Connectivity setup
TCP/IP Screen - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-33
Network setup - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-34
Setup the LOGIQ V2/V1 for DICOM Communications - - - - - - - - - - - - 3-35
How to get the LOGIQ V2/V1 to recognize another Device on the Network - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-37
How to Setup and Use a DICOM Image Storage Service - - - - - - - - - - 3-38
Option Setup
Software Option Installation Procedure - - - - - - - - - - - - - - - - - - - - - - - 3-39
Paperwork after setup
Contents in this Section- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-41
User’s Manual(s) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-41
Product Locator Installation Card - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-41
Chapter 4 — General Procedures and Functional Checks
Overview
Purpose of this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-2
Contents in this chapter- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-2
Special Equipment required - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-2
General procedures
Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-4
Power ON/Boot Up - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-5
Power off - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-9
Logging on to LOGIQ V2/LOGIQ V1 as “ADM” - - - - - - - - - - - - - - - - - 4-11
Service Key (Dongle, HASP) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-12
Exit to Windows Desktop from the LOGIQ V2/LOGIQ V1 application software - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-13
Removable media - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-17
Archiving and loading presets - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-18
Data Management - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-20
Backup - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-20
Restore the factory defaults - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-20
Installation and Setup Procedure for Peripherals - - - - - - - - - - - - - - - - 4-20
Where are the User Manuals and the Service Manual? - - - - - - - - - - - 4-21
How to display or print the PDF files from the Manual CD? - - - - - - - - - 4-21
Cleaning the Trackball- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-22
Functional checks
Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-24
Contents in this Section- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-24
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Preparation - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-24
Basic Controls - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-25
Operator Panel - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-25
Performance Tests - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-26
B mode Checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-27
M Mode Checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-28
Color Mode Checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-29
Adjust the Color Mode controls - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-30
Select Color M Mode- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-31
PW Doppler Mode Checks- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-33
Adjust the PW Doppler Mode controls- - - - - - - - - - - - - - - - - - - - - - - - 4-34
Tissue Velocity Imaging (TVI) Checks- - - - - - - - - - - - - - - - - - - - - - - - 4-35
Adjust the TVI Controls - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-36
Basic Measurements- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-36
Probe/Connectors Check- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-37
Cineloop Check - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-38
Preparation - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-38
Adjust the Cineloop controls - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-38
Back End Processor checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-39
Operator Panel Test - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-39
Peripheral checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-39
Turn OFF Power to LOGIQ V2/LOGIQ V1- - - - - - - - - - - - - - - - - - - - - 4-39
Power supply test & adjustments
Power Supply Test Procedure - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-40
Power Supply Adjustment - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-40
Application Turnover Check List
Software Configuration Checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-41
Site Log
Chapter 5 — Components and Functions (Theory)
Overview
Contents in this chapter- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-2
Block Diagram and Theory
General Information - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-3
Top Console- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-3
Block Diagram - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-4
Power Diagram
Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-5
AC Power - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-5
Common Service Platform
Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-6
Chapter 6 — Service Adjustments
Overview
Contents in this chapter- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-2
LCD Monitor adjustments
Purpose of this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-3
Monitor Adjustments - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-3 i-18 LOGIQ V2/LOGIQ V1 – Basic Service Manual
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Chapter 7 — Diagnostics/Troubleshooting
Overview
Contents in this chapter- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-2
Gathering Trouble Data
Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-3
Collect Vital System Information- - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-3
Collect a Trouble Image with Logs - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-4
Screen Capture
Setting the Store Key to Screen Capture- - - - - - - - - - - - - - - - - - - - - - - 7-6
Capturing a Screen - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-7
Reset the Store Key to Customer’s Functionality - - - - - - - - - - - - - - - - - 7-9
Common Diagnostics
Utilities- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-10
Service Diagnostics - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-15
OP Panel Interface - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-25
Restart the system after diagnostics - - - - - - - - - - - - - - - - - - - - - - - - - 7-25
Network Configuration
Wire-LAN Network - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-26
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
Disassembly/Re-assembly
Warning and Caution - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-5
Tools needed for servicing LOGIQ V2/LOGIQ V1 - - - - - - - - - - - - - - - - 8-6
Trackball Roller Cleaning- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-7
Loading the software
Purpose of this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-8
Customer provided prerequisite - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-8
Data Management - moving all images - - - - - - - - - - - - - - - - - - - - - - - - 8-8
Backing up the Patient Archive and System Configurations - - - - - - - - - 8-9
Recording important settings and parameters - - - - - - - - - - - - - - - - - - - 8-9
Loading the System Software - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-10
Wipe Tool - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-14
Option strings - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-19
Chapter 9 — Renewal Parts
Overview
Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-2
List of Abbreviations
Renewal Parts Lists
AC Power Cord - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-4
Operator Console Assy - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-5
Probe and Accessories - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-6
Peripheral - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-7
Power Cord - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-8
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Manuals- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-9
Chapter 10 — Care and Maintenance
Overview
Contents in this chapter- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-2
Warnings
Why do maintenance
Periodic maintenance inspections - - - - - - - - - - - - - - - - - - - - - - - - - - 10-4
Keeping records - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-4
Quality assurance - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-5
Maintenance task schedule
How often should maintenance tasks be performed? - - - - - - - - - - - - - 10-6
Tools required
Standard GE tool kit - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-8
GE-2 tool kit - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-10
Special tools, supplies and equipment used for maintenance - - - - - - 10-11
System maintenance
Preliminary checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-12
Functional checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-13
Physical inspection - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-15
Optional Diagnostic Checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-16
Probe maintenance- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-17
Electrical safety tests
Safety test overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-19
Leakage current limits - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-21
Outlet test - wiring arrangement - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-23
Grounding continuity - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-24
Chassis leakage current test - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-25
Probe leakage current test- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-27
When there's too much leakage current …
AC/DC Fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-30
Chassis Fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-30
Probe Fails- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-31
Peripheral Fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-31
Still Fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-31
New Unit - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-31
Inspection Paperwork
Ultrasound Inspection Forms - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-32
Electrical Safety Tests Log
Index
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Chapter 1
Introduction
This chapter describes important issues related to safely servicing the Ultrasound system. The service provider must read and understand all the information presented here before installing or servicing the units.
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Introduction
Overview
Contents in this chapter
• ‘Manual Overview’ on page 1-3
• ‘Product icons’ on page 1-10
• ‘Dangerous procedure warnings’ on page 1-21
• ‘Lockout/Tagout (LOTO) requirements’ on page 1-22
• ‘Returning probes and repair parts’ on page 1-23
• ‘EMC, EMI and ESD’ on page 1-24
• ‘Customer assistance’ on page 1-26
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Manual Overview
Manual Overview
This manual provides installation and service information for the
LOGIQ V2/LOGIQ V1 Ultrasound system. It is divided in ten chapters as shown below.
Contents in this manual
The manual is divided into ten chapters.
In the beginning of the manual, before chapter 1, you will find the Revision overview, the Important precautions including
Translation policy, Damage in transportation, Certified electrical
contractor statement, Omission & errors, Service safety
considerations and Legal notes, and the Table of Contents
(TOC).
An Index has been included after Chapter 10.
Chapter number
1.
2.
3.
4.
5.
6.
Table 1-1: Contents in this manual
Chapter title Description
Introduction
Site preparations
System Setup
General Procedures and Functional
Checks
Contains a content summary and warnings.
Contains pre-setup requirements for the LOGIQ
V2/LOGIQ V1.
Contains setup procedure with procedure checklist for the system.
Contains functional checks that must be performed as part of the installation, or as required during servicing and periodic maintenance.
Components and
Functions (Theory)
Contains block diagrams and functional explanations of the electronics.
Service Adjustments Contains instructions on how to make any available adjustments to the LOGIQ V2/LOGIQ
V1.
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Introduction
Table 1-1: Contents in this manual (Continued)
Chapter title Description Chapter number
7.
8.
9.
10.
N/A
Diagnostics/
Troubleshooting
Replacement procedures
Renewal Parts
Provides procedures for running diagnostic or related routines for the LOGIQ V2/LOGIQ V1.
Provides disassembly procedures and reassembly procedures for all changeable FRU.
Contains a complete list of replacement parts for
LOGIQ V2/LOGIQ V1.
Care & Maintenance Provides periodic maintenance procedures for
LOGIQ V2/LOGIQ V1.
Index A quick way to the topic you’re looking for.
Typical users of the Proprietary Service Manual
• GEHC Service Personnel (setup, maintenance, etc.)
• GEHC Online Center Personnel
• Licensed Hospital’s Service Providers
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LOGIQ V2/LOGIQ V1 models covered by this manual
Manual Overview
Table 1-2: LOGIQ V2/LOGIQ V1 Model Designations
Model Number Description
5661244 LOGIQ V2 Generic version
5661242 LOGIQ V1 Generic version
System SW
R1.x.x
R1.x.x
NOTE: When not otherwise specified, the contents of this manual applies to all LOGIQ V2/LOGIQ V1 models.
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Introduction
Important conventions
Conventions used in book
Important conventions, used in this document, are described next.
Model designations
This manual covers the LOGIQ V2/LOGIQ V1 Ultrasound systems listed in:
‘LOGIQ V2/LOGIQ V1 models covered by this manual’ on
page 1-5.
Icons
Pictures, or icons, are used wherever they will reinforce the printed message. The icons, labels, and conventions used on the product and in the service information are described in this chapter.
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Important conventions
Safety precaution messages
Various levels of safety precaution messages may be found on the equipment and in the service information. The different levels of concern are identified by a flag word that precedes the precautionary message. Known or potential hazards to personnel are labeled in one of three ways:
• DANGER
• WARNING
• CAUTION
DANGER
Danger is used to indicate the presence of a hazard that will cause severe personal injury or death if the instructions are ignored.
WARNING
Warning is used to indicate the presence of a hazard that can cause severe personal injury and property damage if instructions are ignored.
CAUTION
Caution is used to indicate the presence of a hazard that will or can cause minor personal injury and property damage if instructions are ignored. Equipment damage possible.
NOTE: Notes are used to provide important information about an item or a procedure.
NOTE: Be sure to read the notes; the information contained in a note can often save you time or effort.
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Introduction
Standard hazard icons
Important information will always be preceded by either the exclamation point (!) contained within a triangle, or the symbols for “Danger”, “Warning” or “Caution”, as seen throughout this chapter. In addition to text, several different graphical icons
(symbols) may be used to make you aware of specific types of hazards that could possibly cause harm. Even if a symbol isn’t used in this manual, it may be included for your reference.
Table 1-3: Standard hazard icons
ELECTRICAL
MECHANICAL
RADIATION
LASER
HEAT
PINCH
NOTE: Even if a symbol isn’t used on the product or in this manual, it may be included for your reference.
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Important conventions
Standard Icons that indicate that a special procedure is to be used
Some others icons make you aware of specific procedures that should be followed.
Table 1-4: Standard Icons that indicates that a special procedure is to be used
Avoid Static Electricity Tag and Lock Out Wear Eye Protection
Hand Protection Foot Protection Wear Eye Protection
Be sure to read the notes; the information contained in a note can often save you time or effort.
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Introduction
Product icons
It is important to refer to the current revision of the Ultrasound system’s User Manual for a full list of product labels prior to servicing the system.
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Labels locations
Labels locations
It is important to refer to the current revision of the Ultrasound system’s User Manual for a full list of product labels prior to servicing the system.
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Introduction
Safety considerations
Contents in this section
Introduction
The following safety precautions must be observed during all phases of operation, service and repair of this equipment.
Failure to comply with these precautions or with specific warnings elsewhere in this manual, violates safety standards of design, manufacture and intended use of the equipment.
Human Safety
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 V2/LOGIQ V1
Training Seminar are authorized to service the equipment.
DANGEROUS VOLTAGES, CAPABLE OF CAUSING
DEATH, ARE PRESENT IN THIS EQUIPMENT. USE
EXTREME CAUTION WHEN HANDLING, TESTING
AND ADJUSTING.
If the covers are removed from an operating LOGIQ V2/LOGIQ
V1, some metal surfaces may be warm enough to pose a potential heat hazard if touched, even while in shutdown mode.
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Safety considerations
Human Safety (continued)
WARNING
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.
WARNING
WARNING
Ensure that the Ultrasound system is turned off and unplugged
Wait for at least 20 seconds for capacitors to discharge as there are no test points to verify isolation. The amber light on the OP panel ON/OFF button will turn off.
Ultrasound system components may be energized. Always refer to the Ultrasound system's Proprietary Service Manual for
LOTO warnings and cautions
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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Introduction
Human Safety (continued)
WARNING
Use all Personal Protection Equipment (PPE) such as gloves, safety shoes, safety glasses, and kneeling pad, to reduce the risk of injury.
WARNING
Beware of possible sharp edges on all mechanical parts. If sharp edges are encountered, the appropriate PPE should be used to reduce the risk of injury.
WARNING
Wear all PPE including gloves as indicated in the chemical
MSDS.
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Safety considerations
Mechanical safety
WARNING
WARNING
WARNING
While the software install procedure is designed to preserve data, you should save any patient data, images, system setups to removable media or hardcopy before doing a software upgrade.
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.
CAUTION
The LOGIQ V2/LOGIQ V1 system weights 6 kg or more, depending on installed peripherals, when ready for use. To avoid possible injury and equipment damage when transporting from one area of use to another:
• Use the handle to move the Ultrasound system.
• Do not let the Ultrasound system strike walls or door frame.
NOTE: Special care should be taken when transporting the Ultrasound system in a vehicle:
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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Introduction
Mechanical safety (continued)
WARNING
When the Ultrasound system is raised for a repair or moved along any incline, use extreme caution since it may become unstable and tip over.
CAUTION
Use protective glasses during drilling, filing smooth surfaces, and during all other work where eyes need protection.
CAUTION
Use safety shoes when doing work where there is any chance of foot injury.
CAUTION
Use protective gloves when working with sharp edges or when directed to wear PPE during a removal/replacement procedure.
CAUTION
Be careful not to pinch any of the cables.
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Safety considerations
Electrical safety
Safe practices
WARNING
Follow these guidelines to minimize shock hazards whenever you are using the Ultrasound system:
• To minimize shock hazard, the equipment chassis must be connected to an electrical ground.
• The Ultrasound system is equipped with a three-conductor
AC power cable. This must be plugged into an approved electrical outlet with safety ground.
• The power outlet used for this equipment should not be shared with other types of equipment.
• Both the system power cable and the power connector must meet international electrical standards
Connecting a LOGIQ V2/LOGIQ V1 to the wrong voltage level will most likely destroy it.
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Introduction
Probes
Peripherals
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
• 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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Safety considerations
Battery Safety
WARNING
To avoid the risk of injury, follow the warning and cautions to make sure that the battery does not burst, ignite, or generate heat of fumes.
• The battery has a safety device. Do not disassemble or alter the battery.
• Charge and discharge the batteries only when the ambient temperature is between 10
° and 40° C (50° F and 104° F).
• Do not short-circuit the battery by directly connecting the negative terminals with metal objects.
• Do not heat the battery or discard it in a fire.
• Do not expose the battery to temperature over 50 ° C
(122 ° F). Keep it away from fire and other heat sources.
• Do not charge the battery near a heat source, such as a fire or heater.
• Do not leave the battery in direct sunlight.
• Do not drop packs from height to prevent them from possible malfunction damage.
• Do not drop packs from height to prevent them from possible malfunction damage.
• Do not pierce the battery with a sharp object, hit it, or step on it.
• Do not use a damaged battery.
• Do not solder a battery.
• Do not connect the battery to an electrical power outlet.
• Do not contact PCM (Power Control and Monitor, it’s a small board in the battery) directly to prevent packs from
ESD damage.
• In case of longer non-use of the LOGIQ V2/LOGIQ V1, please make sure the battery is removed.
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Introduction
Battery Safety (continued)
CAUTION
To avoid the battery bursting, igniting, or fumes from the battery causing equipment damage, observe the following precautions:
• Do not immerse the battery in water or allow it to get wet.
• Do not put the battery into a microwave oven or pressurized container.
• If the battery leaks or emits an odor, remove it from all possible flammable sources.
• If the battery emits an odor or heat, is deformed or discolored, or in a way appears abnormal during use, recharging or storage, immediately remove it and stop using it. If you have any questions about the battery, consult GE or your local representative.
• Short term (less than one month) storage of battery pack:
• Store the battery in a temperature range between-5 ° C
(23 ° F) and 50° C (122°F).
• Use only GE recognized batteries.
• In case of the long term (3 months or more) storage:
• Store the battery in a temperature range of -5 ° C (23°
F) and 50 ° C (122°F).
• When charging for the first time after long-term storage. Recover such packs to original performance through repeating several cycles of full charging and discharging.
• When store packs for more than 6 months, charge at lease once charging require per 6 months to prevent leakage and deterioration in performance due to self-discharging.
• When the system isn't powered on continuously more than
6 months, in order to prevent leakage and deterioration in performance of CMOS battery, power on the system at least once per 6 months for more than 10 hours to have
CMOS battery fully charged. Time and date need to be re-setup.
NOTE: The battery shall be shipped in about 30% charged state. Those packs have to be fully charged and discharged up to 3 times to utilize Li-lon smart packs before use.
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Dangerous procedure warnings
Dangerous procedure warnings
DANGER
WARNING
Warnings, such as the example below, precede potentially dangerous procedures throughout this manual. Instructions contained in the warnings must be followed.
DANGEROUS VOLTAGES, CAPABLE OF CAUSING
DEATH, ARE PRESENT IN THIS EQUIPMENT. USE
EXTREME CAUTION WHEN HANDLING, TESTING
AND ADJUSTING.
If the covers are removed from an operating LOGIQ V2/LOGIQ
V1, some metal surfaces may be warm enough to pose a potential heat hazard if touched, even while in shutdown mode.
WARNING
WARNING
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.
SHUT DOWN FORCEDLY OR PLUG IN/OUT ACDC
INVALID MAY CAUSE THE DAMAGE OF SYSTEM
FILES.
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Introduction
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.
WARNING
4. Remove/disconnect the battery, if present.
6. Control all stored and residual energy.
All potentially hazardous stored or residual energy is relieved.
Energy Control and Power Lockout for LOGIQ V2/LOGIQ V1.
When servicing parts of the Ultrasound system where there is exposure to voltage greater than 30 volts:
1. Follow LOCK OUT/TAG OUT procedures.
2. Turn off the breaker.
3. Unplug the Ultrasound system.
4. Maintain control of the Ultrasound system power plug.
5. Wait for at least 30 seconds for capacitors to discharge as there are no test points to verify isolation.
Ultrasound System components may be energized.
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Returning probes and repair parts
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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Introduction
EMC, EMI and ESD
What is EMC?
Electromagnetic compatibility describes a level of performance of a device within its electromagnetic environment. This environment consists of the device itself and its surroundings including other equipment, power sources and persons with which the device must interface. Inadequate compatibility results when a susceptible device fails to perform as intended due interference from its environment or when the device produces unacceptable levels of emission to its environment. This interference is often referred to as radio–frequency or electromagnetic interference (RFI/EMI) and can be radiated through space or conducted over interconnecting power of signal cables. In addition to electromagnetic energy, EMC also includes possible effects from electrical fields, magnetic fields, electrostatic discharge and disturbances in the electrical power supply.
CE Compliance
LOGIQ V2/LOGIQ V1 conforms to all applicable conducted and radiated emission limits and to immunity from electrostatic discharge, radiated and conducted RF fields, magnetic fields and power line transient requirements.
For applicable standards, refer to the Safety Chapter of the
Ultrasound system User’s Manual.
NOTE: For CE Compliance, it is critical that all covers, screws, shielding, gaskets, mesh, clamps, are in good condition, installed tightly without skew or stress. Proper installation following all comments noted in this service manual is required in order to achieve full EMC performance.
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EMC, EMI and ESD
Electrostatic discharge (ESD) prevention
WARNING
DO NOT touch any boards with integrated circuits prior to taking the necessary ESD precautions.
Always connect yourself, via an arm-wrist strap, to the advised
ESD connection point located on the rear of the Ultrasound system (near the power connector).
Follow general guidelines for handling of electrostatic sensitive equipment.
WARNING
Risk of electrical shock, Ultrasound system must be turned off.
Avoid all contact with electrical contacts, conductors and components. Always use non-conductive handles designed for the removal and replacement of ESD sensitive parts. All parts that have the potential for storing energy must be discharged or isolated before making contact.
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Introduction
Customer assistance
Contact information
If this equipment does not work as indicated in this service manual or in the user manual, or if you require additional assistance, please contact the local distributor or appropriate support resource, as listed below.
Before you call, identify the following information, and acquire image (Alt+D) to send to the Customer Care team:
1. System ID serial number.
3. Date and time of occurrence.
4. Sequence of events leading to issue.
5. Is the issue repeatable?
6. Imaging mode, probe, preset/application.
7. Media brand, speed, capacity, type.
8. Save secondary image capture, cine loop.
NOTE: Restart the application before resuming clinical scanning.
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Customer assistance
Phone numbers for Customer Assistance
LOCATION
USA
GE Healthcare - GE Medical Systems
Ultrasound Service Engineering
9900 Innovation Drive
Wauwatosa, WI 53226
Canada
Latin America
Table 1-5: Phone numbers for Customer Assistance
Europe (OLC-EMEA)
GE Ultraschall Deutschland Gmbh & Co. KG
Beethovenstraße 239
Postfach 11 05 60, D-42655 Solingen
Germany
Online Services Ultrasound Asia
PHONE NUMBER
Service: On-site
Service Parts
1-800-437-1171
1-800-558-2040
Application Support 1-800-682-5327 or
1-262-524-5698
Phone: 1-800-668-0732
Service
Application Support
OLC - EMEA
Phone:
Fax:
1-800-321-7937
1-262-524-5698
+49 (0) 212 2802 - 652
+33 1 3083 1300
+49 (0) 2122-8024-31
Phone:
• Australia
• China
• India
• Japan
• Korea
• Singapore
+(61) 1-800-647-855
+(86) 800-810-8188
+(91) 1800-425-8025
+(81) 42-648-2940
+(82) 2620 13585
+(95) 6277-3444
System manufacturer
Table 1-6: System manufacturer
MANUFACTURER
GE Medical Systems (China) Co., Ltd.
No.19 Changjiang Road
WuXi National Hi-Tech Development Zone
Jiangsu
P.R.China 214028
PHONE NUMBER
+86 510 85225888
FAX NUMBER
+86 510 85226688
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Introduction
Authorized Representative
Table 1-7: Authorized Representative
AUTHORIZED REPRESENTATIVE
The location of the CE marking is shown in the Safety chapter of the User manual.
TELEPHONE / FAX
NUMBER
+49 761 45 43 -0 /
+49 761 45 43 -233
Authorized EU Representative/European registered place of business:
GE Medical Systems Information Technologies GmbH (GEMS IT GmbH)
Munzinger Strasse 5, D-79111 Freiburg, GERMANY
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Chapter 2
Site Preparations
This chapter provides the information required to plan and prepare for the setup of an Ultrasound system.
Included are descriptions of the facility and electrical needs to be met by the purchaser of the units.
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Site Preparations
Overview
Contents in this chapter
• ‘General Ultrasound system requirements’ on page 2-3
• ‘Facility needs’ on page 2-12
• ‘Environmental Dangers’ on page 2-22
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General Ultrasound system requirements
General Ultrasound system requirements
Contents in this section
page 2-3
• ‘Probes environmental requirements’ on page 2-11
• ‘Time and manpower requirements’ on page 2-11
Ultrasound system environmental requirements
If the Ultrasound system is very cold or hot
When unpacking the Ultrasound system, allow the temperature of the Ultrasound system to stabilize before powering up. The following table describes guidelines for reaching operational temperatures from storage or transport temperatures.
Degree C
Degree F hours
CAUTION
If the Ultrasound system is very cold or hot, do not turn on its power until it has had a chance to acclimate to its operating environment.
Table 2-1: System Acclimation Time Chart
50 45 40 35 30 25 20 15 10 5 0 -5
122 113 104 95 86 77 68 59 50 41 32 23
4
2
0
0 0 0 0 0 0 2 4 6
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Site Preparations
Environmental specifications for Ultrasound system
Temperature
Humidity
Pressure
The system should be operated, stored, or transported within the parameters outlined below. Either its operational environment must be constantly maintained or the unit must be turned off.
Table 2-2: System Environmental Requirements
Operational
10° - 40°C
50° - 104°F
30 - 80% non-condensing
700 - 1060hPa
Storage
-5° - 50°C
23° - 122°F
10 - 90% non-condensing
700 - 1060hPa
Transport (<16hrs.)
-5° - 50°C
23° - 122°F
10 - 90% non-condensing
700 - 1060hPa
CAUTION
Ensure that the probe face temperature does not exceed the normal operation temperature range.
CAUTION
The LOGIQ V2/LOGIQ V1 system and probe connector is not waterproof. Do not expose the device to water or any kind of liquid.
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General Ultrasound system requirements
Cooling
Lighting
The cooling requirement for a console Ultrasound system with monitor and on board peripherals, is up to 3800 BTU/h. This figure does not include cooling needed for lights, people, or other equipment in the room.
NOTE: Each person in the room places an additional 300 BTU/h demand on the cooling system.
Bright light is needed for Ultrasound system installation, updates and repairs. However, operator and patient comfort may be optimized if the room light is subdued and indirect. Therefore a combination lighting system (dim/bright) is recommended. Keep in mind that lighting controls and dimmers can be a source of
EMI which could degrade image quality. These controls should be selected to minimize possible interference.
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Site Preparations
Electrical requirements
General requirements
NOTE: GE requires a dedicated power and ground for the proper operation of its Ultrasound equipment. This dedicated power shall originate at the last distribution panel before the Ultrasound system.
Sites with a mains power system with defined Neutral and Live:
The dedicated line shall consist of one phase, a neutral (not shared with any other circuit), and a full size ground wire from
the distribution panel to the Ultrasound outlet.
Sites with a mains power system without a defined Neutral:
The dedicated line shall consist of one phase (two lines), not shared with any other circuit, and a full size ground wire from the
distribution panel to the Ultrasound outlet.
NOTE: Please note that image artifacts can occur, if at any time within the facility, the ground from the main facility's incoming power source to the Ultrasound system is only a conduit.
Electrical requirements for the Ultrasound system
In the table below, the electrical specifications for the Ultrasound system includes monitor and on board peripherals.
Table 2-3: Electrical Specifications for LOGIQ V2/LOGIQ V1 system
Voltage
100-240 VAC
Tolerance
±10%
Power Consumption
Max. 200VA
Frequency
50/ 60HZ
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General Ultrasound system requirements
Site circuit breaker
CAUTION
CAUTION
Site power outlets
Power outage may occur. The LOGIQ V2/LOGIQ V1 requires a dedicated single branch circuit. To avoid circuit overload and possible loss of critical care equipment, make sure you do not have any other equipment operating on the same circuit.
It is recommended that the branch circuit breaker for the
Ultrasound system be readily accessible.
POWER OUTAGE MAY OCCURE.
The LOGIQ V2/LOGIQ V1 requires a dedicated single branch circuit. To avoid circuit overload and possible loss of critical care equipment, make sure you DO NOT have any other equipment operating on the same circuit.
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.
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Site Preparations
Power stability requirement
IEC 61000-4-11
Voltage dips, short interruptions and voltage variations on mains supply
Table 2-4: Power stability requirement
< 5%T (> 95% dip) for
0.5 cycle;
40%T (60% dip) for 5 cycles;
70%T (30 dip) for 25 cycles;
< 5%T (>95% dip) for 5 sec
< 5%T (> 95% dip) for
0.5 cycle;
40%T (60% dip) for 5 cycles;
70%T (30 dip) for 25 cycles;
< 5%T (>95% dip) for 5 sec
Mains power quality should be that of a typical commercial or hospital environment.
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General Ultrasound system requirements
EMI limitations
Ultrasound systems are susceptible to Electromagnetic
Interference (EMI) from radio frequencies, magnetic fields, and transients in the air or wiring. They also generate EMI. The
Ultrasound system complies with limits as stated on the EMC label. However there is no guarantee that interference will not occur in a particular installation.
Possible EMI sources should be identified before the Ultrasound system is installed.
Electrical and electronic equipment may produce EMI unintentionally as the result of a defect. Some of these sources include:
• scanners
• computers
• monitors
• fans
• in-house wireless phones (DECT phones)
• wireless computer keyboard and mouse
• air conditioning system
• High Frequency (HF) surgery equipment
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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2-9
Site Preparations
EMI prevention/abatement
EMI RULE
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
Table 2-5: EMI prevention/abatement
DETAILS
• Keep the Ultrasound system at least 5 meters (15 feet) away from other EMI sources.
• Special shielding may be required to eliminate interference problems caused by high frequency, high powered radio or video broadcast signals.
Poor grounding is the most likely reason an Ultrasound system will have noisy images. Check grounding of the power cord and power outlet.
• After you finish repairing or updating the Ultrasound system, replace all covers and tighten all screws.
• Any cable with an external connection requires a magnet wrap at each end.
• Install all covers. Loose or missing covers or Radio Frequency gaskets allow radio frequencies to interfere with the ultrasound signals.
If more than 20% or a pair of the fingers on an Radio Frequency gasket are broken, replace the gasket. Do not turn on the Ultrasound system until any loose metallic part is removed.
Where applicable, never place a label where Radio Frequency gaskets meet the
Ultrasound system. Otherwise, the gap created will permit Radio Frequency leakage. Or, if a label has been found in such a position, move the label.
The interconnect cables are grounded and require ferrite beads and other shielding. Also, cable length, material, and routing are all important; do not change from what is specified.
Cellular phones may transmit a 5 V/m signal; that could cause image artifacts.
Where applicable, do not allow cables to lie across the top of the Card Rack or hang out of the peripheral bays. Loop the excess length for peripheral cables inside the peripheral bays. Attach the monitor cables to the frame.
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General Ultrasound system requirements
Probes environmental requirements
Operation, storage and transport temperatures for probes
Probes should be operated, stored, or transported within the parameters outlined below.
CAUTION
Ensure that the probe face temperature does not exceed the normal operation temperature range.
Temperature
Humidity
Pressure
CAUTION
Table 2-6: Probe Environmental Requirements
Operational
10
° - 40° C
50
° - 104° F
30- 80% non-condensing
700 - 1060hPa
Storage
-5
° - 50° C
23
° - 122° F
10 - 90% non-condensing
700 - 1060hPa
Transport
-5
° - 50° C
23
° - 122° F
10 - 90% non-condensing
700 - 1060hPa
Check the room temperature before you use the probe.
CAUTION
Ensure that the probe face temperature does not exceed the normal operation temperature range.
NOTE: Refer to Table 2-1 on page 2-3 to determine the needed settlement time.
Time and manpower requirements
Site preparation takes time. Begin site preparation checks as soon as possible, if possible, six weeks before delivery, to allow enough time to make any changes.
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Site Preparations
Facility needs
Contents in this section
• ‘Purchaser responsibilities’ on page 2-13
• ‘Required facility needs’ on page 2-14
• ‘Desirable features’ on page 2-15
• ‘Minimal floor plan suggestion’ on page 2-16
• ‘Recommended floor plan suggestion’ on page 2-17
• ‘Suggested floor plan, Ultrasound system, and EchoPAC PC in same room’ on page 2-18
• ‘Networking setup requirements’ on page 2-19
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Facility needs
Purchaser responsibilities
The work and materials needed to prepare the site is the responsibility of the purchaser. Delay, confusion, and waste of manpower can be avoided by completing pre-installation work before delivery. Purchaser responsibility includes:
• Procuring the materials required
• Completing the preparations before delivery of the
Ultrasound system
• Paying the costs for any alterations and modifications not specifically provided in the sales contract
NOTE: All electrical installations that are preliminary to the positioning of the equipment at the site prepared for the equipment must be performed by licensed electrical contractors. Other connections between pieces of electrical equipment, calibrations, and testing must also be performed by qualified personnel. The products involved (and the accompanying electrical installations) are highly sophisticated and special engineering competence is required. All electrical work on these products must comply with the requirements of applicable electrical codes. The purchaser of GE equipment must only utilize qualified personnel to perform electrical servicing on the equipment.
The desire to use a non–listed or customer provided product or to place an approved product further from the Ultrasound system than the interface kit allows, presents challenges to the installation team. To avoid delays during installation, such variances should be made known to the individuals or group performing the installation at the earliest possible date
(preferably prior to the purchase).
The ultrasound suite must be clean prior to delivery of the
Ultrasound system. Carpet is not recommended because it collects dust and creates static. Potential sources of EMI
(electromagnetic interference) should also be investigated before delivery. Dirt, static, and EMI can negatively impact
Ultrasound system reliability.
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Site Preparations
Required facility needs
NOTE: GE requires a dedicated power and ground for the proper operation of its Ultrasound equipment. This dedicated power shall originate at the last distribution panel before the Ultrasound system.
Sites with a mains power system with defined Neutral and Live:
The dedicated line shall consist of one phase, a neutral (not shared with any other circuit), and a full size ground wire from
the distribution panel to the Ultrasound outlet.
Sites with a mains power system without a defined Neutral:
The dedicated line shall consist of one phase (two lines), not shared with any other circuit, and a full size ground wire from the
distribution panel to the Ultrasound outlet.
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Facility needs
Required facility needs (continued)
NOTE: Please note that image artifacts can occur, if at any time within the facility, the ground from the main facility's incoming power source to the Ultrasound unit is only a conduit.
• Dedicated single branch power outlet of adequate amperage meeting all local and national codes which is located less than 2.5 m (8 ft.) from the unit’s proposed location
• Door opening is at least 76 cm (30 in) wide
• Proposed location for unit is at least 0.5m (1.5 ft.) from the wall for cooling
• Power outlet and place for any external peripheral are within
2 m (6.5 ft.) of each other with peripheral within 1 m of the unit to connect cables.
• Power outlets for other medical equipment.
• Power outlets for test equipment within 1 m (3.2 ft.) of
Ultrasound system.
• Clean and protected space to store probes (in their cases or on a rack)
• Material to safely clean probes (done with a plastic container, never metal)
For the amperage requirements, see: ‘Electrical requirements’ on page 2-6.
Desirable features
• Door is at least 92 cm (3 ft.) wide
• Circuit breaker for dedicated power outlet is easily accessible
• Sink with hot and cold water
• Receptacle for bio–hazardous waste, like used probe sheaths
• Storage for linens and equipment
• Nearby waiting room, lavatory, and dressing room
• Dual level lighting (bright and dim)
• Lockable cabinet ordered by GE for its software and proprietary manuals
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Site Preparations
Minimal floor plan suggestion
CSI 8x10
Scale:
Each square equals one square foot (app. 31 x 31 cm)
2
3
4 5
11
7
9
8
10
13
12
6
14
1
1. Door – at least 762 mm (30 inches)
3. Counter Top, Sink with hot and cold water and Supplies
Storage
5. Probes/Supplies
6. Examination Table – 1930 x
610 mm (76 x 24 inches)
7. Footswitch
8. Stool
10. External Peripherals
11. Dedicated Power Outlet -
Circuit Breaker protected and easily accessible
12. Network Interface
13. 457 mm (18 inches) distance of Ultrasound system from wall or objects
14. GE Cabinet for Software and
Manuals
Figure 2-1. Minimal floor plan, 2.5 m x 3 m (8 by 10 foot)
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Facility needs
Recommended floor plan suggestion
CSI 14x17
10
11
12
15
9
13 14
16
2
3
4
5
8
7
1
17
6
18
Scale: Each square equals one square foot (app. 31 x 31 cm)
1. Secretaries or Doctors Desk
5. Counter Top and Sink with hot and cold water
6. Overhead Lights Dimmer -
Dual Level Lighting (bright and dim)
10. Dedicated Power Outlet -
Circuit Breaker protected and easily accessible
11. Network Interface
12. 457 mm (18 inches) distance of Ultrasound system from wall or objects
13. Stool
14. Footswitch
15. Storage for Linens and
Equipment
16. Examination Table – 1930 x
610 mm (76 x 24 inches)
17. Lavatory and Dressing Room
18. Door – at least 762 mm (30 inches)
Figure 2-2. A 14 by 17 foot recommended floor plan
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Site Preparations
Suggested floor plan, Ultrasound system, and EchoPAC PC in same room
1. EchoPAC PC workstation parts
2. UPS
3. Ethernet network wall outlet
4. 3x mains power outlets
5. Hot and Cold water
6. Dedicated mains power outlet
7. Ethernet network wall outlet
Figure 2-3. Suggested Room with EchoPAC PC workstation and Ultrasound Scanner
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Networking setup requirements
Stand alone Ultrasound system (without network connection)
Facility needs
None.
Scanner connected to hospital’s network
InSite requirements
Supported networks:
100/1000 Mbit Ethernet/DICOM network
Wireless LAN
InSite requires an Ethernet connection via:
• 100/1000 Mbit Interface
Purpose of the DICOM network function
DICOM services provide the operator with clinically useful features for moving images and patient information over a hospital network.
Examples of DICOM services include the transfer of images to workstations for viewing or transferring images to remote printers.
As an added benefit, transferring images in this manner frees up the on-board monitor and peripherals, enabling viewing to be done while scanning continues.
With DICOM, images can be archived, stored, and retrieved faster, easier, and at a lower cost.
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Site Preparations
DICOM option setup requirements
To configure the Ultrasound system to work with other network connections, the site’s network administrator must provide information to complete the form “Worksheet for DICOM
Network Information”. Ensure that there are no spaces in any field of the form.
See:
Entries must include:
• A host name, local port number, AE Title, IP address and
Net Mask for the Ultrasound system.
• The IP addresses for the default gateway and other routers at the site for ROUTING INFORMATION.
• The host name, IP address, port and AE Title for each device the site wants connected to the Ultrasound system for DICOM APPLICATION INFORMATION. A field for the make (manufacturer) and the revision of the device, is also included. This information may be useful for error solving.
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DICOM option setup requirements (continued)
Facility needs
Figure 2-4. Worksheet for DICOM Network Information
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Site Preparations
Environmental Dangers
Commercial devices such as laser cameras, printers, VCRs and external monitors, usually exceed allowable leakage current limits and, when plugged into separate AC outlets, are in violation of patient safety standards. Suitable electrical isolation of such external AC outlets, or providing the device with extra protective earth, will be required in order to meet IEC60601-1 standards for electrical leakage.
Patient Environment IEC60601-1 and ANSI AAMI ES60601-1
Sub Clause 3.79 and figure A.9 (IEC60601-1:2005 and ANSI AAMI
ES60601-1:2005)
Such an area is an environment in which medical diagnosis, monitoring or treatment is carried out. It is very difficult to attach unique dimensions to the PATIENT
ENVIROMENT.
In practice a distance of 2,5 m (8.2 ft.) above the floor on which the medical personnel stand and a horizontal distance of 1,5 m (4.9 ft.) have justified themselves as indicative of the dimensions of the Patient Environment.
The patient environment/vicinity will be depicted as a dashed line in this procedure.
See example below.
2-22
Figure 2-5. Patient environment
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Chapter 3
System Setup
This chapter contains information needed to install
LOGIQ V2/LOGIQ V1 system.
Included is a procedure that describes how to receive and unpack the equipment and how to file a damage or loss claim.
How to prepare the facility and unit of the actual installation, and how to check and test the unit, probes, and external peripherals for electrical safety are also included in this procedure.
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3-1
System Setup
Overview
Contents in this chapter
• ‘Setup reminders’ on page 3-3
• ‘Receiving and unpacking the equipment’ on page 3-6
• ‘Preparing for setup’ on page 3-13
• ‘Completing the setup’ on page 3-14
• ‘System Configuration’ on page 3-18
• ‘Connectivity setup’ on page 3-33
• ‘Paperwork after setup’ on page 3-41
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Setup reminders
Setup reminders
Average setup time
• Unpacking the LOGIQ V2/LOGIQ V1: 20 minutes
• Set up LOGIQ V2/LOGIQ V1 options: 15 minutes
• DICOM Network Configuration: 30 minutes or more, depending on the configuration
• Install Insite: 0.5 hour
The LOGIQ V2/LOGIQ V1 installation and functional checkout will take approximately one hour. LOGIQ V2/V1 consoles with optional equipment may take slightly longer.
Setup warnings
DANGER
WHEN USING ANY TEST INSTRUMENT THAT IS CAPABLE
OF OPENING THE AC GROUND LINE (I.E., METER’S
GROUND SWITCH IS OPEN), DON’T TOUCH THE
ULTRASOUND SYSTEM!
CAUTION
To prevent electrical shock, connect the unit to a properly grounded power outlet. DO NOT use a three to two prong adapter. This defeats safety grounding.
CAUTION
DO NOT wear the ESD wrist strap when you work on live
circuits and more than 30 V peak is present.
CAUTION
DO NOT operate this unit unless all board covers and frame
panels are securely in place. System performance and cooling require this.
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3-3
System Setup
Setup warnings (continued)
NOTE:
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.
For information regarding packing labels, refer to LABELS
ON PACKAGE.
2. After being transported, the unit may be very cold or hot. If this is the case, allow the unit to acclimate before you turn it on. It requires one hour for each 2.5°C increment it's temperature is below 3°C or above 40°C.
DANGER
Equipment damage possibility. Turning the system on without acclimation after arriving at site may cause the system to be damaged.
CAUTION
If the Ultrasound system is very cold or hot, do not turn on its power until it has had a chance to acclimate to its operating environment.
Degree C
Degree F hours
The following table describes guidelines for reaching operational temperatures from storage or transport temperatures.
Table 3-1: System Acclimation Time Chart
50 45 40 35
122 113 104 95
4 2 0 0
30
86
0
25
77
0
20
68
0
15
59
0
10
50
0
5
41
2
0
23
4
-5
23
6
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Setup reminders
Setup warnings (continued)
CAUTION
CAUTION
Operator Manual(s)
The User Manual(s) should be fully read and understood before operating the LOGIQ V2/LOGIQ V1 and kept near the
Ultrasound system for quick reference.
Acoustic Output Hazard
Although the ultrasound energy transmitted from the LOGIQ
V2/LOGIQ V1 probe is within AIUM/NEMA standards, avoid unnecessary exposure. ultrasound energy can produce heat and mechanical damage.
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3-5
System Setup
Receiving and unpacking the equipment
Purpose of this section
This section describes how to receive and unpack the
LOGIQ V2/LOGIQ V1.
Contents in this section
• ‘Warnings for receiving and unpacking’ on page 3-6
• ‘Receiving the LOGIQ V2/LOGIQ V1’ on page 3-6
• ‘Unpacking the LOGIQ V2/LOGIQ V1’ on page 3-8
Warnings for receiving and unpacking
CAUTION
Remember to use relevant personal protecting equipment
(PPE) during packing and unpacking. Check with your local
EHS representative.
Receiving the LOGIQ V2/LOGIQ V1
Overview
Improper handling during transportation may harm the equipment inside the package even if the package itself is undamaged.
Examine all packages
Examine package closely at time of delivery, as described in the procedure below.
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Receiving and unpacking the equipment
Damage in transportation
Follow this procedure if damage is apparent:
1. Write “Damage In Shipment” on ALL copies of the freight or express bill BEFORE delivery is accepted or “signed for “by a GE representative or hospital receiving agent.
2. Report the damage to the carrier.
• Whether noted or concealed, damage MUST be reported to the carrier immediately upon discovery, or in any event, within 14 days after receipt, and the contents and containers held for inspection by the carrier.
damage if an inspection is not requested within this 14 day period.
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3-7
System Setup
Unpacking the LOGIQ V2/LOGIQ V1
When a new system arrives, check that any components are not damaged and are not in short supply. If shipping damage or shortage occurs, contact the address shown in Chapter 1
CAUTION
Please carefully unpack the system, and do not dispose the package of LOGIQ V2/V1, so that it can be reused for service.
NOTE: Please check the LOGIQ V2/V1 console is well assembly after unpacking the system.
1. Cut the adhesive tape and open top covers of paper carton.
Figure 3-1. Open Top Covers of Paper Carton
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Receiving and unpacking the equipment
Unpacking the LOGIQ V2/LOGIQ V1 (continued)
2. Take out console together with 2 interleavers from console package.
3. Take out the interleavers beside Accessories Package
4. Take out Accessories Package.
CAUTION
Figure 3-2. Unpacking the equipment
Do not lift the unit by the rubber band. Equipment damage may result.
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3-9
System Setup
Unpacking the LOGIQ V2/LOGIQ V1 (continued)
5. Remove 2 interleavers.
Figure 3-3. Removing interleavers and plastic bag
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Receiving and unpacking the equipment
Unpacking the LOGIQ V2/LOGIQ V1 (continued)
NOTE: Check the shipping container for special instructions. Verify that the container is intact. In some cases a secondary container may be used. If so, ask the carrier for unpacking instructions.
Moving into Position
Figure 3-4. Labels on Package
CAUTION
Do not lift the unit by the rubber band. Use handle to move system.
CAUTION
Equipment Damage Possibility. Lifting the console by holding covers may damage the covers. Do not lift the console by holding any covers.
In general, a single adult can move the LOGIQ V2/V1. Before moving, store all loose parts in original accessory box or in back pack. Return probes to original box.
Packing the Equipment
Please pack LOGIQ V2/V1 in the reverse order of unpacking.
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System Setup
Packing materials - recycling information
The packing materials for LOGIQ V2/LOGIQ V1 are recyclable:
• The Transportation Box is made of spruce or similar material. (“PHYTOSANITARY CERTIFICATE” included in all shipments to The People's Republic of China.)
• Lever lockings (hinges) are made of zinc plated steel.
• The inner reinforcements are made of Ethafoam
(Polyethylene foam).
• The plastic foil is made of LDPE (Low Density
Polyethylene).
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Preparing for setup
Preparing for setup
Verify customer order
Compare items received by the customer to that which is listed on the delivery order. Report any items that are missing, back ordered, or damaged.
Physical inspection
Verify that the system arrived intact (visual inspection).
If the system has been damaged, please refer to ‘Damage in transportation’ on page i-11 in the beginning of this manual.
EMI protection
The LOGIQ V2/LOGIQ V1 has been designed to minimize the effects of Electro-Magnetic Interference (EMI). Many of the covers, shields, and screws are provided primarily to protect the system from image artifacts caused by this interference. For this reason, it is imperative that all covers and hardware are installed and secured before the unit is put into operation.
See ‘EMI limitations’ on page 2-9 for more information about
EMI protection.
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System Setup
Completing the setup
Purpose of this section
This section describes how to complete the installation of
LOGIQ V2/LOGIQ V1.
Contents in this section
• ‘System specifications’ on page 3-14
• ‘Electrical specifications’ on page 3-15
• ‘Peripheral/Accessories Connector Panel’ on page 3-16
• ‘Powering the system’ on page 3-17
System specifications
System requirements verification
Physical dimensions
• 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.
Height
120
4.72
Table 3-2: Physical dimensions of LOGIQ V2/LOGIQ V1
Length
396
15.59
Width
368
14.49
Unit
mm
Inches
Console Weight
• Weight: approx. 6 kg (13.23 lbs)
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Completing the setup
Electrical specifications
WARNING
Connecting a LOGIQ V2/LOGIQ V1 to the wrong voltage level will most likely destroy it.
Verification of the system’s voltage setting
Verify that the mains voltage specified for the LOGIQ V2/LOGIQ
V1 is available on-site.
Refer to the latest revision of the User Manual for a full list of product labels prior to serving the system.
Electrical specifications for LOGIQ V2/LOGIQ V1
Part
Number
5661244
5661242
In the table below, the electrical specifications for LOGIQ V2/
LOGIQ V1 includes monitor and on board peripherals.
Table 3-3: Electrical specifications for LOGIQ V2/LOGIQ V1
Voltage Tolerances
Power consumntion Frequency Description
LOGIQ V2 Generic version
LOGIQ V1 Generic version
100-240V ±10% Max.200VA
50/60 Hz
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System Setup
Peripheral/Accessories Connector Panel
LOGIQ V2/V1 peripherals and accessories can be properly connected using the side connector panel.
3-16
Figure 3-5. Rear and left Side Connector Panel
2. Port for DC In (AC Adapter)
3. Composite Out Port
4. S-Video Out Port
NOTE:
7. Isolated USB Port for AC Printer ONLY
The AC printer can be connected to this isolated USB port only.
8. USB Ports for Footswitch, DVD-RW, Wirelss LAN Adapter,
USB Stick, USB HDD
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Completing the setup
Peripheral/Accessories Connector Panel (continued)
NOTE: Accessory equipment connected to the analog and digital interfaces must be certified according to the respective IEC standards (e.g. IEC60950 for data processing equipment and
IEC60601-1 for medical equipment). Furthermore, all complete configurations shall comply with the valid version of the system standard IEC60601-1. Everybody who connects additional equipment to the signal input part or signal output part of LOGIQ
V2/LOGIQ V1, configures a medical system, and is therefore responsible that the Ultrasound system complies with the requirements of the valid version of IEC60601-1. If in doubt, consult the technical service department or your local representative for GE.
Connecting probes
Please refer to User Manual on how to connect/disconnect a probe.
Powering the system
Please refer to User Manual on how to power the system.
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System Setup
System Configuration
Purpose of this section
This section describes how to configure the LOGIQ V2/V1.
LOGIQ V2/V1 configuration
For complete instructions, refer to the latest revision of the
LOGIQ V2/V1 Basic User Manual, Chapter 16.
Information includes Entering Location, Adjusting Date and
Time, Selecting User interface Language, Selecting Online
Manual Language, Selecting Unites of Measure.
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Peripherals Installation
Peripherals Installation
Overview
Description
B/W USB Printer
B/W USB Printer
B/W USB Printer
Color USB Printer
Officejet 100 Printer
Officejet Pro 8100 Printer
1-Pedal Footswitch
3-Pedal Footswitch
USB Stick
USB3.0 HDD
USB3.0 HDD
USB3.0 HDD
Wireless Adapter
Probe Adapter
This section describes how to install and configure the peripherals validated for the LOGIQ V2/V1.
About the operation check-out of peripherals, See ‘Peripheral checks’ on page 4-39 for more information.
Table 3-4: LOGIQ V2/V1 Peripherals
Control
USB port
USB port
USB port
USB port
USB port
USB port
USB port
USB port
USB port
USB port
USB port
USB port
USB port
Probe port
Model
Sony UP-D897 Printer
Sony UP-D898MD Printer
Sony UP-D711MD Printer
Sony UP-D25MD Printer
HP Officejet 100 Printer
HP Officejet Pro 8100 Printer
Footswitch FSU-1000
MKF 2-MED GP26
Keeber USB Flash Drive 8G
WD Elements 2.5 in USB3.0 HDD 1TB
Seagate Backup Plus 2.5 in USB3.0 HDD 1TB
Seagate Expansion 2.5 in USB3.0 HDD 1TB
Edimax wireless adapter AC1200
2 Probe Port Extension Adapter
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System Setup
Furnished materials
This section describes the materials furnished with the
Peripherals and with the system.
Retain the original carton and packing materials in case transport is needed in the future.
Item
3
4
1
2
Table 3-5: Materials furnished with B/W Printer
Description
Sony UP-D897 Printer
Sony UP-D898MD Printer
Paper Roll
USB cable
Quantity
1
1
1
1
Note
Item
1
2
3
4
• Color USB Printer
Table 3-6: Materials furnished with Color USB Printer
Description
Sony UP-D25MD Printer
Paper Roll
AC Power Cord (local purchase)
USB cable
Quantity
1
1
1
1
Note
Item
3
4
1
2
Table 3-7: Materials furnished with B/W Printer
Description
HP Officejet 100 Printer
HP Officejet Pro 8100 Printer
Paper Roll
USB cable
Quantity
1
1
1
1
Note
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Peripherals Installation
Furnished materials (continued)
Item
1
2
3
Table 3-8: Materials furnished with USB Stick
Description
Keeber USB Flash Drive 8G
Paper Roll
USB cable
Quantity
1
1
1
Note
Item
1
2
Table 3-9: Materials furnished with the USB HDD
Description
USB HDD
USB Cable
Quantity
1
1
Note
Item
1
2
• Footswitch
Table 3-10: Materials furnished with the Footswitch
Description
1 Pedal Footswitch
3 Pedal Footswitch
Quantity
1
1
Note
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System Setup
Peripherals Installation Instructions
Sony UP-D25MD Printer Installation
Tools
No special tools needed.
Manpower
One person 5 min.
Preparations
1. Unpack the Sony UP-D25MD Printer.
Installation Procedure
1. Place the device in a suitable place.
2. Connect the USB Cable and power cable on the Printer.
3. Connect the power cord in the wall outlet, then turn on the printer.
4. Connect USB cable to LOGIQ V2/V1 USB port.
3-22
Figure 3-6. Color printer Connection
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Sony UP-D25MD Printer Installation (continued)
Peripherals Installation
NOTE:
Figure 3-7. Connectivity->Service printer from the Printer pull-down Properties menu. Type the printer name in the Name Filed. This name is used on the
Button screen. After you select the printer from the Printer pull-down Properties menu again, it turns white. Press
Save.
After selecting the printer, the field turns white.
Figure 3-8. Select the Printer
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System Setup
Sony UP-D25MD Printer Installation (continued)
Print3) from the Physical Print Butoons selection. Select the printer from MyComputer column and press >> to move it to the Printflow View column. PressSave.
Figure 3-9. Select Button
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Peripherals Installation
HP Officejet 100 Printer Installation
Tools
No special tools needed.
Manpower
One person 5 min.
Preparations
1. Unpack the HP Officejet 100 Printer.
Installation Procedure
1. Place the device in a suitable place.
2. Connect the USB Cable on the Printer.
3. Connect the power cord with the AC output in the wall outlet, then turn on the printer.
4. Connect USB cable to LOGIQ V2/V1 USB port.
Figure 3-10. HP Officejet 100 connection
5. Refer to the Connectivity configure steps of ‘Sony
UP-D25MD Printer Installation’ on page 3-22.
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System Setup
HP Officejet Pro 8100 Printer Installation
Tools
No special tools needed.
Manpower
One person 5 min.
Preparations
1. Unpack the HP Officejet Pro 8100 Printer.
Installation Procedure
1. Place the device in a suitable place.
2. Connect the USB Cable on the Printer.
3. Connect the power cord with the AC output in the wall outlet, then turn on the printer.
4. Connect USB cable to LOGIQ V2/V1 USB port.
Figure 3-11. HP Officejet Pro 8100 connection
5. Refer to the Connectivity configure steps of ‘Sony
UP-D25MD Printer Installation’ on page 3-22.
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Peripherals Installation
UP-D897 Printer Installation
Tools
No special tools needed.
Manpower
One person 5 min.
Preparations
1. Unpack the UP-D897 Printer.
Installation Procedure
1. Place the device in a suitable place.
2. Connect the USB Cable on the Printer.
3. Connect the power cord with the AC output in the wall outlet, then turn on the printer.
4. Connect USB cable to LOGIQ V2/V1 USB port.
Figure 3-12. UP-D897 connection
5. Refer to the Connectivity configure steps of ‘Sony
UP-D25MD Printer Installation’ on page 3-22.
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System Setup
UP-D898MD Printer Installation
Tools
No special tools needed.
Manpower
One person 5 min.
Preparations
1. Unpack the UP-D898MD Printer.
Installation Procedure
1. Place the device in a suitable place.
2. Connect the USB Cable on the Printer.
3. Connect the power cord with the AC output in the wall outlet, then turn on the printer.
4. Connect USB cable to LOGIQ V2/V1 USB port.
3-28
Figure 3-13. UP-D898 connection
5. Refer to the Connectivity configure steps of ‘Sony
UP-D25MD Printer Installation’ on page 3-22.
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Peripherals Installation
Footswitch Installation
Tools
No special tools needed.
Manpower
One person 2 min.
Preparations
2. Ensure no physical damage.
Installation Procedure
1. Connect the Footswitch to the USB port on the LOGIQ V2/
V1 system.
Figure 3-14. Connect Footswitch to the system
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System Setup
Footswitch Installation (continued)
Configuring Footswitch
Footswitch supports these configurations: No Function, Freeze,
Next Heartcycle, Prev Heartcycle, Print1, Print2, Update, Next
Step (Scan Assistant), Previous Step (Scan Assistant), Scan
Assistant pause/Resume.
Enter Utility -> Application-> Settings to configure the
Footswitch functions.
Figure 3-15. Configuring Footswitch Functions
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Peripherals Installation
USB HDD Installation
Tools
No special tools needed.
Manpower
One person 1 min.
Preparations
1. Unpack the USB HDD.
2. Ensure no physical damage.
Installation Procedure
1. Connect the USB HDD to the USB port on the LOGIQ V2/V1 system.
Figure 3-16. Connect HDD to the system
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System Setup
Wireless LAN Adapter Installation
Tools
No special tools needed.
Manpower
One person 1 min.
Preparations
1. Unpack the Wireless LAN Adapter.
2. Ensure no physical damage.
Installation Procedure
1. Connect the Wireless LAN Adapter to the USB port on the
LOGIQ V2/V1 system.
Figure 3-17. Connect Wireless LAN Adapter to the system
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Connectivity setup
Connectivity setup
TCP/IP Screen
to ‘Logging on to LOGIQ V2/LOGIQ V1 as “ADM”’ on
page 4-11 .
network settings for LOGIQ V2/V1.
Figure 3-18. TCP/IP Screen
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System Setup
Changing the AE title and/or Port Number
To change AE Title and/or Port Number, edit the respective fields.
Figure 3-19. AE Title/Port No
Network setup
For network connection setup, See ‘Network Configuration’ on
page 7-26 for more information.
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Connectivity setup
Setup the LOGIQ V2/V1 for DICOM Communications
LOGIQ V2/LOGIQ V1 is configured to work with DICOM servers in a network environment. Images are first saved on the local image butter on the system. At the end of the examination the images are sent to the DICOM server via a DICOM spooler and to the local database, depending on dataflows.
To connect to the DICOM server, the following information has to be entered in the system.
• The DICOM server IP address
• The DICOM server port number
• The DICOM server AE title (the server application's name)
Table 3-11: Utility ->Connectivity ->TCP/IP screen
1
2
Enter the
LOGIQ V2/V1
computer name. This may be the same as the station name.
Enter the
LOGIQ V2/V1
IP address, subnet mask, default gateway and network speed.
For automatic assignment of IP address, subnet mask and default gateway, select
DHCP.
Note: If possible, set the
LOGIQ V2/V1
network Speed to match that of the Network switch. if in doubt, set it to AutoDetect. Otherwise, transfer times can be two or five times longer, during which the
LOGIQ V2/V1
will appear to be locked up. (If the Hard Drive activity light on the front of the console is lit steady or blinks quickly, the
LOGIQ V2/V1
is most likely not hung.)
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System Setup
Setup the LOGIQ V2/V1 for DICOM Communications (continued)
Table 3-12: Utility ->Connectivity ->Device screen
1
2
3
Select MyComputer.
Assign an AE title to the
LOGIQ V2/V1
. (AE stands for Application Entity. DICOM services use this to identify the
LOGIQ V2/V1
.) AE title is case-sensitive. This title may contain the Computer Name from the TCP/IP page, if desired.
Note: It is NOT recommended to use the factory default. This is not prohibited, but more than one system with the same AE title can cause confusion.
Edit Port Number if needed. 104 is typical. Save your changes and reboot the system.
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Connectivity setup
How to get the LOGIQ V2/V1 to recognize another Device on the
Network
Table 3-13: Utility ->Connectivity ->Device screen
1
2
3
Select Add. The system creates a device called “NewDevice”.
Change the name to one of your choosing.
Enter the IP address of the device.
4 Save your changes and then press Ping. A “Smiley Face” indicates successful communication between your LOGIQ V2/V1 and the device. A “Frown” indicates failed communication. Check the following:
• Is the device running?
• Is it connected to the network?
• Did you enter the right IP address?
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System Setup
How to Setup and Use a DICOM Image Storage Service
An Image Storage Service provides a place to store patient and exam data from LOGIQ V2/V1 and corresponding images. The
Image Storage Service, or the device that hosts it, is often called a Patient Archiving and Communication System (PACS).
Table 3-14: Setup an Image Storage Service
2
3
4
4
1 In Utility -> Connectivity -> Service, from the Destination Device drop-down menu, select the device on which the service resides. (This assumes you have already setup the device in the Device tab in
‘How to Setup and Use a DICOM Image Storage Service’ on
page 3-38
.
From the Select Service Type to add drop-down menu, select DICOM Image Storage and press Add.
Change the name of the service to one of your choosing.
Enter the AE Title and port Number of the service. AE Title is case-sensitive.
Save your changes and then press Verify. A “Smiley Face” indicates successful communication with the service.
Note: If you get a successful Ping (Smiley Face) at the device level but not at the service level, it is possible that the AE Title or Port Number of the service settings are incorrect. Ensure that these are correct then re-verify. Be sure that the service type
(Store, Print, etc) is correct and supported by the device.
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Option Setup
Option Setup
Software Option Installation Procedure
NOTE: Not all features described in this section may be available or cleared for sale in all markets. Please contact with your local GE
Ultrasound representative to get the latest information.
NOTE:
1. Power on the system.
Keep the power cord connection during the installation.
2. After the power-up sequence is complete, press Utility on the control panel, and then select Admin.
WARNING
For software Option Installation, the operator must login as
Administrator.
select Add.
Figure 3-20. New Option Key
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System Setup
Software Option Installation Procedure (continued)
NOTE:
Figure 3-21. Dialog Window
There is no need to restart the system after each installation, if several option keys are installed at one time.
Select Cancel for the first several times, and select OK after the last installation to activate all the changes.
5. After the system is powered on, check the option status.
The option status explanation:
• Valid: This option is enabled in the system.
6. Exit and check the function of the option installed.
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Paperwork after setup
Paperwork after setup
NOTE: During and after setup, the documentation (i.e. CDs with documentation, User Manuals, Installation Manuals, etc.) for the
LOGIQ V2/LOGIQ V1 and the peripherals must be kept as part of the original Ultrasound system documentation. This ensures that all relevant safety and user information is available during the operation and service of the complete Ultrasound system.
Contents in this Section
• ‘User’s Manual(s)’ on page 3-41
• ‘Product Locator Installation Card’ on page 3-41
User’s Manual(s)
User Check that the correct User Manual(s) for the system and software revision, is included with the installation. Specific language versions of the User Manual may also be available.
Check with your GE Sales Representative for availability.
Product Locator Installation Card
NOTE: The Product Locator Installation Card shown may not be the same as the provided Product Locator card.
Figure 3-22. Product Locator Installation Card (Example)
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3-41
System Setup
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Chapter 4
General Procedures and
Functional Checks
This chapter provides procedures for quickly checking major functions of the LOGIQ V2/LOGIQ V1 and diagnostics instructions using the built-in service software.
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4-1
General Procedures and Functional Checks
Overview
Purpose of this chapter
This chapter provides procedures for quickly checking major functions of the scanner and diagnostics instructions using the built-in service software.
Contents in this chapter
• ‘Overview’ on page 4-2
• ‘General procedures’ on page 4-3
• ‘Functional checks’ on page 4-24
• ‘Power supply test & adjustments’ on page 4-40
Special Equipment required
To perform these tests, you'll need any of the sector, linear, or convex probes. (Normally you should check all the probes used on the system).
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General procedures
General procedures
CAUTION
WARNING
Ultrasound system requires all covers.
Operate this Ultrasound system only when all board covers and frame panels are securely in place. The covers are required for safe operation, good Ultrasound system performance and cooling purposes.
Energy Control and Power Lockout for LOGIQ V2/LOGIQ V1.
When servicing parts of the Ultrasound system where there is exposure to voltage greater than 30 volts:
1. Follow LOCK OUT/TAG OUT procedures.
2. Turn off the breaker.
3. Unplug the Ultrasound system.
4. Maintain control of the Ultrasound system power plug.
5. Wait for at least 30 seconds for capacitors to discharge as there are no test points to verify isolation.
Ultrasound System components may be energized.
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4-3
General Procedures and Functional Checks
Overview
Some procedures are used more often than other. The intention with this section is to keep the most used procedures in one place.
Contents in this section
• ‘Power ON/Boot Up’ on page 4-5
• ‘Power off’ on page 4-9
• ‘Logging on to LOGIQ V2/LOGIQ V1 as “ADM”’ on
page 4-11
• ‘Service Key (Dongle, HASP)’ on page 4-12
• ‘Exit to Windows Desktop from the LOGIQ V2/LOGIQ V1 application software’ on page 4-13
• ‘Removable media’ on page 4-17
• ‘Archiving and loading presets’ on page 4-18
• ‘Data Management’ on page 4-20
• ‘Backup’ on page 4-20
• ‘Cleaning the Trackball’ on page 4-22
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General procedures
Power ON/Boot Up
Warnings
DANGER
DANGER
ALWAYS CONNECT THE ULTRASOUND SYSTEM TO A
FIXED POWER SOCKET WHICH HAS THE PROTECTIVE
GROUNDING CONNECTOR.
NEVER USE A THREE-TO-TWO PRONG ADAPTER; THIS
DEFEATS THE SAFETY GROUND.
DANGER
ENSURE THAT THE POWER CORD AND PLUG ARE
INTACT AND THAT THE POWER PLUG IS THE PROPER
HOSPITAL-GRADE TYPE (WHERE REQUIRED).
CAUTION
CAUTION
Ultrasound system requires all covers.
Operate this Ultrasound system only when all board covers and frame panels are securely in place. The covers are required for safe operation, good Ultrasound system performance and cooling purposes.
Use only power supply cords, cables and plugs provided by or designated by GE.
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4-5
General Procedures and Functional Checks
Connect AC (mains) Power to LOGIQ V2/LOGIQ V1
Lower the handle. Plug the AC adapter output connector into the system DC input port (located on the system’s rear panel) with the arrow side upward. Plug the AC adapter power cord into a grapunded, protective earth outlet.
After AC/DC is connected correctly to the scanner, the power is applied to the scanner. When the Power On/Off key is pressed once, the System starts.
Figure 4-1. Connect AC Adapter
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General procedures
Switch ON the AC Power to LOGIQ V2/LOGIQ V1
NOTE:
Press once on the On/Off key on the Operator Panel to boot the unit.
During a normal boot, you may observe that: a. The unit’s ventilation fan starts on full speed, but slows down after a few seconds (listen to the fan sound).
b. Power is distributed to the peripherals, Operator Panel
(Console), Monitor, Front End Processor and Back End
Processor.
c. Back End Processor and rest of scanner starts with the sequence listed in the next steps: d. Back End Processor is turned ON and starts to load the software.
e. The Start Screen is displayed on the monitor.
f. A start-up bar indicating the time used for software loading, is displayed on the monitor.
g. The software initiates and sets up the Front End electronics and the rest of the instrument.
h. The backlight in the keyboard is lit.
i. As soon as the software has been loaded, either a 2D screen is displayed on the screen, indicating that a probe has been connected, or a No Mode screen is displayed, indicating that no probe has been connected.
Total time used for start-up is typical one and a half minutes or less. If starting after a power loss or a lock-up, the start-up time may be up to four minutes.
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4-7
General Procedures and Functional Checks
Check System Date and Time
A warning message “Please check the system date and time are correct” appears on the screen when the system is powered on.
This warning message appears for the possible reasons:
• The system is not boot up for over 14 days.
• The system time has been changed by 24 hours earlier than the current system time of last boot-up.
This warning message is to remind the user to check the system date in case the system date and time is incorrect.
Figure 4-2. Check system date and time message
Move the cursor to OK and press Cursor key on the control panel to select OK. The system enters scanning mode.
Check the system date and time. If it is incorrect, follow below steps to reset the system date and time.
1. Enter Utility -> System -> General -> Date/Time.
2. Reset the system date and time.
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Power off
General procedures
When you switch off the unit, the system performs an automatic shutdown sequence.
The SYSTEM - EXIT menu, used when switching off the unit, gives you these choices:
NOTE:
Figure 4-3. System Exit Window
•
Logoff
Use this button to log off the current user.
The system remains ON and ready for a new user to log on.
If the Logoff button is dimmed, it indicates that no user is logged on to the unit at the moment.
•
Shutdown
Use this button to shut down the system. The entire system will shut down. It is recommended to perform a full shutdown at least once a week.
If the Shutdown button is dimmed, use the key-combination
<Ctrl+Alt+Delete> to shut down the unit.
To enable the key-combination <Ctrl+Alt+Delete>, the dongle should be connected to the system.
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General Procedures and Functional Checks
Power off (continued)
•
Exit
(Only available when logged in as GE Service with Service
Dongle)
Select this button when you want to exit to Windows
Desktop.
•
Cancel
Use this button to exit from the System-Exit menu and return to the previous operation.
System shutdown
Disconnect the Mains Power Cable is necessary. For example:
Relocating the scanner.
CAUTION
DO NOT unplug and/or transport the unit until after the power off sequence has been completed. Failure to do so may result in corrupted patient files.
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General procedures
Logging on to LOGIQ V2/LOGIQ V1 as “ADM”
Select Utility -> Admin -> System Admin.
It will bring up the Operator Login dialog where you must log on.
Figure 4-4. Operator Login Window
1. Operator: Select the operator.
2. Password: Enter Operator’s password (optional).
3. Select the type of Login or Cancel.
•
OK: Standard login.
•
Cancel: Cancel login.
As default, two users are defined, USR and ADM.
• USR
If you log on as USR, you will have access to do set-up tasks that a user may need to do during daily use.
• ADM
If you log on as ADM, you will have access to do general set-up, service adjustments, adjust network and connectivity settings.
Select the name ADM, the password and select Login.
It is possible for the administrator (ADM) to establish new users and set unique passwords for each user, including a new password for ADM. If the login as ADM fails, contact the responsible person in the hospital to get access.
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General Procedures and Functional Checks
Service Key (Dongle, HASP)
A Service Dongle and a proprietary GE Service password are necessary for use by GE Service when performing proprietary level diagnostics like accessing the desktop on the BEP. The password used with the GE service dongle changes at specific intervals.
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General procedures
Exit to Windows Desktop from the LOGIQ V2/LOGIQ V1 application software
Follow these steps if you want to exit to the Windows Desktop when the application software is running. The Service Dongle must be plugged in.
1. On the alphanumeric keyboard, press Ctrl+Alt+Delete and then select Task Manager.
Process.
Figure 4-5. Windows Security
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General Procedures and Functional Checks
Exit to Windows Desktop from the LOGIQ V2/LOGIQ V1 application software (continued)
Figure 4-6. Maintenance Access
4-14
Figure 4-7. Task Warning
Service Password in the Password field.
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General procedures
Exit to Windows Desktop from the LOGIQ V2/LOGIQ V1 application software (continued)
NOTE:
Figure 4-8. Maintenance Access
READ THIS NOTE BEFORE YOU CONTINUE: After you have selected OK, the Start Application dialog will be displayed on screen. Be ready to select MAINTENANCE... before the Time Bar is “full”, or the application software will be started. A description on how to recover, if you fail to select MAINTENANCE... is included, but you will spend
some extra time doing it.
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General Procedures and Functional Checks
Exit to Windows Desktop from the LOGIQ V2/LOGIQ V1 application software (continued)
will bring up the Maintenance dialog.
Figure 4-9. System halted will display the Windows Desktop on the screen.
4-16
Figure 4-10. Maintenance dialog
NOTE: If you need to restart, ensure that you do a complete power down (Shut Down). This is required to power up the Front End
Processor.
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General procedures
Removable media
Refer to the latest revision of the User Manual to perform the following tasks:
• Formatting Removable Media
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General Procedures and Functional Checks
Archiving and loading presets
NOTE: Always save presets before any software reload. This ensures the presets loaded after the software reload are as up–to–date as possible.
All user presets except changes to Summary, Anatomy, and
Biometry pages, can be saved on an DVD-R disk (or USB memory device) for reloading on the system.
NOTE: Presets should NOT be saved on the same USB memory device
(or DVD-R disk) as images. The Archive Menu lists the images but does NOT list the presets stored on a USB memory device
(or DVD-R disk, SD Card).
Archiving Presets to a USB memory device (or DVD-R Disk, SD Card)
1. Connect the USB memory device to the system’s USB port, or insert an empty (blank) DVD-R disk into the DVD-RW.
2. EnterUtility -> System -> Backup/Restore. The Backup/
Restore sheet will be shown on the LCD display.
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Figure 4-11. Backup Sheet
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General procedures
Archiving Presets to a USB memory device (or DVD-R Disk, SD Card)
(continued)
3. Select the item to Backup.
4. Enter backup destination or browse through the disk to locate the destination.
5. Select Backup. The backup status for each item is displayed on the Result column.
Loading Presets from a USB memory device (or DVD-R)
1. Connect the USB memory device or DVD-R with the archived Presets to the system.
Restore sheet will be shown on the LCD display. See
Figure 4-11 on page 4-18.
3. Select the items needed to be restored.
4. Select Restore. The system performs the restore and restarts.
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General Procedures and Functional Checks
Data Management
Refer to the latest revision of the LOGIQ V2/LOGIQ V1 User
Manual to perform the following tasks:
• Configuring the Disk Management Function
• Setting the Disk Management Schedule
• Configuring Data Management Settings
• Configuringestination Device Setting
• Running the Disk Management Function
• Starting Disk Management Manually
Backup
For more information, refer to the latest revision of the LOGIQ
V2/LOGIQ V1 User Manual.
Restore the factory defaults
For instructions, please see “Data Backup and Restore” in the
User Manual/User Guide.
Installation and Setup Procedure for Peripherals
Please refer to ‘Peripherals Installation Instructions’ on
page 3-22
.
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General procedures
Where are the User Manuals and the Service Manual?
Online versions of the User Manuals are available via the help function.
Both the User Manuals and the Service Manual are delivered as
PDF files on a CD-ROM. Paper copies may be ordered from
GE.
How to display or print the PDF files from the Manual CD?
1. Insert the CD-R disk (CD-ROM) into the CD-drive on a PC or Laptop with Adobe Acrobat Reader.
CAUTION
Do not try to use the LOGIQ V2/LOGIQ V1 to read these files, it will not work!
2. Follow the instructions on the screen to display the manual of choice.
3. Before printing the complete manual, or pages from the manual, select File > Page Setup.
you may choose which pages to print and the number of copies you want to print (usually 1 copy).
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General Procedures and Functional Checks
Cleaning the Trackball
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.
Manpower
One person, 5 minutes,
Tools
• Antistatic brush and/or antistatic vacuum cleaner
Preparations
To get access to the trackball for cleaning, you must perform the following steps:
1. Power down the system.
2. Disconnect the mains power cable from the wall outlet.
Follow these links if you need more information: See ‘Power off’ on page 4-9 for more information.
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General procedures
Clean the Trackball
Dust is often building up behind the ball, so it interferes with the ball rotation and for optical trackballs the light used for sensing.
To get access for cleaning, you need to remove the ball.
The ball is held in position by the Dust Gasket.
1. Power off the system.
2. Rotate the dust gasket counterclockwise until it can be removed from the keyboard.
CAUTION
Figure 4-12. Remove the retainer
3. Separate the trackball and the gasket. Wipe off any oil or dust from the trackball, gasket and the trackball housing using a cleaner or cotton swab.
4. Assemble the trackball and gasket, then put it into the housing and rotate it clockwise until its notches are set in the position.
When cleaning, make sure not to spill or spray any liquid into the trackball housing (keyboard or system).
Test the Trackball
Power up the system and test that the trackball now works as intended.
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General Procedures and Functional Checks
Functional checks
Overview
In this section, the functional checks for LOGIQ V2/LOGIQ V1 are described. Functional checks are used to verify that the product works as intended. Functional checks may also be used during troubleshooting.
Contents in this Section
Preparation
Turn on power to LOGIQ V2/LOGIQ V1. For detailed description, See ‘Power ON/Boot Up’ on page 4-5 for more
information.
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Basic Controls
Operator Panel
Functional checks
2. Primary menu Key
4. TGC
6. User Defined keys
10. Preset Key
Figure 4-13. Control Panel Map
11. Worksheet key
12. End Exam key
13. Archive key
14. Gain/AO keys
15. Scan Coach keys
16. Mode keys
17. Cursor key
18. Clear key
19. Comment key
20. Active key
21. Measure key
22. Body Pattern key
23. M/D Cursor key
24. Scan Area key
25. Set/B Pause key
26. Trackball
27. Depth/Zoom/Ellipse key
28. Left/Right key
29. Freeze key
30. Print key
31. Store key
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General Procedures and Functional Checks
Performance Tests
Test Phantoms
The use of test phantoms is only recommended if required by your facility's (customer’s) QA program.
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Functional checks
B mode Checks
Introduction
The B Mode is the system’s default mode.
B Mode Screen Example
Preparations
• Connect one of the probes.
• Turn ON the scanner.
The B Mode is displayed (default mode).
Adjust the B mode controls
Press B on the Operator Panel to access B mode.
These Image Controls are used to optimize the B Mode picture.
Verify that all the listed controls are working as intended: together with the Power control.
interest.
(move to lower frame rate) to increase resolution in image.
penetration.
• Use the DDP control to optimize imaging in the blood flow regions and make a cleaner, less noisy image.
reduce image speckle. Extra care must be taken to select the optimal Speckle reduction level, as too much filtering of speckle can mask or obscure desired image detail.
and blood pol artifact without diluting tissue appearance of moving structures.
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General Procedures and Functional Checks
M Mode Checks
M-Mode Screen Example
Preparations
• Connect one of the probes to the scanner’s left-most probe connector.
• Turn ON the scanner.
The 2D Mode window is displayed (default mode).
picture on the screen.
Use the trackball to position the cursor over the required area of the image.
Adjust the M Mode controls
These Image Controls are used to optimize the M mode picture.
Verify that all the listed controls are working as intended:
Adjust Gain and TGC controls to adjust the range to be imaged.
Use the Frequency (move to higher frequencies) or the
Frame rate control (move to lower frame rate) to increase
resolution in image.
Use the Frequency (move to lower frequency) to increase penetration.
Adjust Focus to move the focal point(s) around the region of interest in the M-Mode display.
Adjust Dynamic range to optimize the useful range of incoming echoes to the available grey scale.
Adjust Compress and Edge Enhance to further optimize the display.
Adjust Reject to reduce noise while taking care not to eliminate significant low-level diagnostic information.
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Functional checks
Color Mode Checks
Introduction
Color Flow screens are 2D or M Mode screens with colors representing blood or tissue movement.
Color Flow may be selected both from 2D mode or from M mode or a combination of these.
Preparations
• Connect one of the probes to the scanner’s left-most probe connector.
• Turn ON the scanner.
The B Mode window is displayed (default mode).
Select Color Mode
1. From an optimized B Mode image, press CF.
2. Use the trackball to position the ROI frame over the area to be examined.
highlighted in the trackball status bar. Use the trackball to adjust the dimension of the ROI.
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General Procedures and Functional Checks
Adjust the Color Mode controls
NOTE:
NOTE:
NOTE:
area.
Adjust Scale to the highest setting that provides adequate flow detection.
The scale value may affect FPS, Low Velocity Reject, and
Sample Volume.
Adjust Low Velocity Reject to remove low velocity blood flow and tissue movement that reduces image quality.
Adjust Variance to detect flow disturbances.
Adjust Sample volume (SV) to a low setting for better flow resolution, or a higher setting to more easily locate disturbed flows.
Adjust Frequency to optimize the color flow display. Higher settings improve resolution. Lower settings improve depth penetration and sensitivity. This does not affect the frequency used for 2D and M-Mode.
Frequency setting may affect FPS, SV and Low Velocity
Reject.
Adjust Power to obtain an acceptable image using the lowest setting possible.
The Power setting affects all other operating modes.
Adjust the following settings to further optimize display of the image: area of the display.
Use Tissue priority to emphasize either the color flow overlay, or the underlying grey scale tissue detail.
Use Baseline to emphasize flow either toward or away from the probe.
Use Radial and Lateral Averaging to reduce noise in the color flow area. Radial and Lateral Averaging smooths the image by averaging collected data along the same horizontal line. An increase of the lateral averaging will reduce noise, but this will also reduce the lateral resolution.
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Functional checks
Select Color M Mode
1. Select M Mode.
2. Use the trackball to position the ROI frame over the area to be examined.
the trackball status bar. Use the trackball to adjust the dimension of the ROI.
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General Procedures and Functional Checks
Adjust the Color M Mode controls
NOTE:
NOTE:
NOTE:
• Adjust the Active mode gain to set the gain in the color flow area.
Adjust Scale to the highest setting that provides adequate flow detection.
The scale value may affect FPS, Low Velocity Reject, and
Sample Volume.
Adjust Low Velocity Reject to remove low velocity blood flow and tissue movement that reduces image quality.
Adjust Variance to detect flow disturbances.
Adjust Sample volume (SV) to a low setting for better flow resolution, or a higher setting to more easily locate disturbed flows
Adjust Frequency to optimize the color flow display. Higher settings improve resolution. Lower settings improve depth penetration and sensitivity. This does not affect the frequency used for 2D and M-Mode.
NOTE: Frequency setting may affect FPS, SV and Low
Velocity Reject.
Adjust Power to obtain an acceptable image using the lowest setting possible.
The Power setting affects all other operating modes.
Adjust the following settings to further optimize display of the image: area of the display.
Use Tissue priority to emphasize either the color flow overlay, or the underlying grey scale tissue detail.
Use Baseline to emphasize flow either toward or away from the probe.
Use Radial and Lateral Averaging to reduce noise in the color flow area. Radial and Lateral Averaging smooths the image by averaging collected data along the same horizontal line. An increase of the lateral averaging will reduce noise, but this will also reduce the lateral resolution.
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Functional checks
PW Doppler Mode Checks
Introduction
PW Doppler are used to measure velocity (most often in blood).
Doppler mode can be done with a special pencil probe or with an ordinary probe. By using an ordinary probe, you can first bring up a 2D picture for navigation purpose and then add PW
Doppler.
Preparations
• Connect one of the probes to the scanner.
• Turn ON the scanner.
The 2D Mode window is displayed (default mode).
• If needed, adjust the Display’s Brightness and Contrast setting.
Press PW to start Pulsed Wave Doppler (PW).
Use the trackball to select the Area of Interest (Sample
Volume) in PW.
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General Procedures and Functional Checks
Adjust the PW Doppler Mode controls
Adjust the Active mode gain to set the gain in the spectral
Doppler area.
NOTE:
NOTE:
blood flow and tissue movement.
In PW mode, adjust Sample volume to low setting for better resolution, or higher setting to more easily locate the disturbed flows.
Adjust the Compress setting to balance the effect of stronger and weaker echoes and obtain the desired intensity display.
Adjust Frequency to optimize flow display. Higher setting will improve resolution and the lower setting will increase the depth penetration.
Adjust Frame rate to a higher setting to improve motion detection, or to a lower setting to improve resolution.
Frequency and Frame rate settings may affect the Low
Velocity Reject.
The Doppler Power setting affects only Doppler operating modes.
Adjust the following settings to further optimize the display of the image.
Use the Horizontal sweep to optimize the sweep speed.
To view signal detail, adjust Scale to enlarge the vertical spectral Doppler trace.
Use Invert to reverse the vertical component of the spectral
Doppler area of the display.
Use Angle correction to steer the ultrasound beam to the blood flow to be measured.
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Functional checks
Tissue Velocity Imaging (TVI) Checks
Introduction
TVI calculates and color codes the velocities in tissue. The tissue velocity information is acquired by sampling of tissue
Doppler velocity values at discrete points. The information is stored in a combined format with grey scale imaging during one or several cardiac cycles with high temporal resolution.
Preparations
NOTE:
• Connect one of the probes, to the scanner’s left-most probe connector.
• Turn ON the scanner.
The 2D Mode window is displayed (default mode).
• If needed, adjust the Display’s Brightness and Contrast setting.
Press TVI.
Use the trackball (assigned function: Pos) to position the
ROI frame over the area to be examined.
Press Select. The instruction Size should be highlighted in the trackball status bar.
If the trackball control pointer is selected, press trackball to be able to select between Position and Size controls.
Use the trackball to adjust the dimension of the ROI.
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General Procedures and Functional Checks
Adjust the TVI Controls
NOTE:
NOTE:
• To reduce quantification noise (variance), the Nyquist limit should be as low as possible, without creating aliasing. To reduce the Nyquist limit: Reduce the Scale value.
The Scale value also affects the frame rate. There is a trade off between the frame rate and quantification noise.
TVI provides velocity information only in the beam direction.
The apical view typically provides the best window since the beams are then approximately aligned to the longitudinal direction of the myocardium (except near the apex). To obtain radial or circumferential tissue velocities, a parasternal view must be used. However, from this window the beam cannot be aligned to the muscle for all the parts of the ventricle.
PW will be optimized for Tissue Velocities when activated from inside TVI.
Basic Measurements
NOTE: The following instructions assume that you first scan the patient and then press Freeze.
Check Distance and Tissue Depth Measurement
2. Move the trackball to position the active caliper at the start point (distance) or the most anterior point (tissue depth).
4. The system fixed the first caliper and displays a second active caliper.
5. Move the trackball to position the second active caliper at the end point (distance) or the most posterior point (tissue depth).
displays the distance or tissue depth value in the measurement results window.
NOTE: To toggle between active calipers, rotate Cursor Select button.
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Functional checks
Probe/Connectors Check
NOTE: Probes can be connected at any time, whether the unit is ON or
OFF.
Connecting a Probe
CAUTION
1. Place the probe’s carrying case on a stable surface and open the case.
2. Carefully remove the probe and unwrap the probe cable.
3. Put the porbe in the probe holder.
DO NOT allow the probe head to hang free. Impact to the probe head could result in irreparable damage.
4. Align the connector with the probe port and carefully push into place.
5. Lock the probe latch upward.
4
5
Step
1
2
3
6 not resting on the floor.
Table 4-1: Probe and Connectors Checks
Task
Select the appropriate connected probe from the probe indicators on the Touch Panel.
Expected Results
The probe activates in the currently-selected operating mode. The probe’s default settings for the mode and selected exam are used automatically.
The selected application starts.
Launch the application. To change application without changing the current probe, press Model on the Touch Panel.
Verify there’s no EMI/RFI or artifacts specific to the probe.
Test the probe in each active connector slot.
Do a leakage test on the probe, See ‘Electrical safety tests’ on page 10-19 for more information.
Repeat this procedure for all available probes.
No EMI/RFI or artifacts.
It will display pictorial data each time.
It passes the test.
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General Procedures and Functional Checks
Cineloop Check
Introduction
A cineloop is a sequence of images recorded over a certain time frame. When using ECG the time frame can be adjusted to cover one or more heart cycles. When frozen, the System automatically displays the cineloop boundary markers on either side of the last detected heart cycle.
Preparation
• Connect one of the probes to the scanner.
• See for info about connecting the probes
For available probes, see ‘Probe and Accessories’ on
page 9-6
:
• Turn ON the scanner. The 2D Mode is displayed (default mode).
Adjust the Cineloop controls
The left and right markers are displayed on either side of the last detected heart cycle on the ECG trace.
The selected heart beat is played back.
Use the trackball to scroll through the acquisition and find the sequence of interest.
and select the heart cycle of interest.
Adjust Num cycles to increase or decrease the number of heart beats to be played back.
Adjust Left marker and Right marker to trim or expand the cineloop boundaries.
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Functional checks
Back End Processor checks
• If all the previous tests have been passed successfully, the
Back End Processor is most likely OK.
If the system seems to be operating erratically, please refer to ‘Diagnostics/Troubleshooting’ on page 7-1 .
Operator Panel Test
• The Operator Panel is tested when the LOGIQ V2/LOGIQ
V1 is powered up as part of the start-up scripts, run at every start-up.
For more info, please refer to ‘Diagnostics/Troubleshooting’ on page 7-1 .
Peripheral checks
Printer checks
The internal printer is controlled from the Print and Store keys on the LOGIQ V2/LOGIQ V1’s Operator Panel.
The factory default is:
•
Print for the standard printer
Store for the screen capture to clipboard
Turn OFF Power to LOGIQ V2/LOGIQ V1
See ‘Power off’ on page 4-9 for more information.
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General Procedures and Functional Checks
Power supply test & adjustments
Power Supply Test Procedure
There is no need to do any special tests on the Power Supplies if there don’t seems to be a problem that may be related to the
Power Supply.
Power Supply Adjustment
There are no adjustments on the power supply. The DC Power is self-regulated. If a voltage is outside the specified range, it means that something is wrong, either with the power supply itself or with a unit connected to that specific power outlet. When an error occur, the power will be turned off immediately.
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Application Turnover Check List
Application Turnover Check List
Complete these checks before returning the scanner to customer for use:
Software Configuration Checks
3
4
1
2
5
Step
Table 4-2: Software Configuration Checks
Task to do
Verify Date and Time is correct.
Verify that Location (Hospital Name) is correct.
Verify Language settings are correct.
Verify assignment of Print Keys.
Verify all of the customer’s options are set up correctly.
Notes
Demo Option strings turn on
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General Procedures and Functional Checks
Site Log
DATE
Table 4-3: Site Log
SRVICE PERSON PROBLEM COMMENTS
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Chapter 5
Components and Functions
(Theory)
This chapter explains LOGIQ V2/LOGIQ V1’s system concepts, component arrangement, and subsystem functions.
It also describes the power distribution and the
Common Service Desktop interface.
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5-1
Components and Functions (Theory)
Overview
Contents in this chapter
• ‘Block Diagram and Theory’ on page 5-3
• ‘Power Diagram’ on page 5-5
• ‘Common Service Platform’ on page 5-6
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Block Diagram and Theory
Block Diagram and Theory
General Information
LOGIQ V2/LOGIQ V1 is an ultrasound imaging scanner.
The system can be used for:
• 2D Gray Scale
• 2D Color Flow imaging
• M-Mode Gray Scale imaging
• Doppler
• Different combinations of the above
Signal flow from the Probe Connector Panel to the Front End, to the Mid Processors and Back End Processor and finally to the
LCD and peripherals.
System configuration is stored on a hard disk drive and all necessary software is loaded from the hard disk drive on power up.
Top Console
The Top Console includes a Standby/On switch, a keyboard, different controls for manipulating the picture quality, controls for use in Measure & Analyze (M&A), and loudspeakers for stereo sound output (used during Doppler scanning).
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Components and Functions (Theory)
Block Diagram
System Diagram
Introduction
Figure 5-1. LOGIQ V2/LOGIQ V1 System Block Diagram
AC-DC adapter provides DC power input to WDC PWA.
WDC PWA is main power supply for the system, it provides multi powers to MST PWA and IO PWA.
MST provides the main control function, 64 channels transmitting/receiving and related signal processing, and connects to CWD board.
IO board receives MISC signals from MST board and make necessary processing, it provides multi-user interface (such as
HDMI, LAN, USB, S-Video etc.).
PFPC board shall transfer 64 channels to 128 channels for RS type probe.
KBD Assy provides multi function keyboard.
2PP adapter shall expand the RS probe port quantity to two.
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Power Diagram
Power Diagram
Overview
AC Power
The AC Power assy’s main tasks are to isolate and output to the
DC/DC unit which is inside the system console. The input of AC power pack will be the AC outlet and it’s universal, the range is
AC 100V-240V, 50-60Hz. And no main power switch located on this power pack.
LOGIQ V2/LOGIQ V1 Power supply is an ACDC adapter which use 100V-240V (50-60Hz) as input and DC 19V (7.9A) as output.
Figure 5-2. ACDC Adapter
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Components and Functions (Theory)
Common Service Platform
Introduction
The Service Platform contains a set of software modules that are common to all PC backend ultrasound and cardiology systems. The Common Service Platform will increase service productivity and reduce training and service costs.
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Chapter 6
Service Adjustments
This chapter describes how to test and make adjustments to the LOGIQ V2/LOGIQ V1. You can use these to test the system for errors.
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Service Adjustments
Contents in this chapter
• ‘LCD Monitor adjustments’ on page 6-3
Overview
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LCD Monitor adjustments
LCD Monitor adjustments
Purpose of this section
This section describes how to test and adjust the scanner.
These tests are optional. You may use them to check the system for errors.
Monitor Adjustments
To adjust the brightness and volume:
1. On the alphanumeric keyboard,
Figure 6-1. Monitor Adjustment
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Service Adjustments
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Chapter 7
Diagnostics/Troubleshooting
This chapter describes LOGIQ V2/LOGIQ V1how to setup and run the tools and software that help maintain image quality and system operation. Very basic host, system and board levels are run whenever power is applied. Some Service Tools may be run at the application level.
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Diagnostics/Troubleshooting
Contents in this chapter
• ‘Gathering Trouble Data’ on page 7-3
• ‘Network Configuration’ on page 7-26
Overview
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Gathering Trouble Data
Gathering Trouble Data
Overview
There may be a time when it would be advantageous to capture trouble images and system data (logs) for acquisition to be sent back to the manufacturer for analysis. There are different options to acquire this data that would give different results
Collect Vital System Information
The following information is necessary in order to properly analyze data or images being reported as a malfunction or being returned to the manufacturer:
Product Name = LOGIQ V2/LOGIQ V1
From the Utility > System > About screen:
Applications Software
System Image Software
• Image Part Number
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7-3
Diagnostics/Troubleshooting
Collect a Trouble Image with Logs
If the system should malfunction, press the Alt+D keys simultaneously. This will collect a screen capture of the image monitor, system presets and several log files in a date and time stamped “.zip” file.
NOTE: This function may also be used to make a Print Screen.
This Alt+D function is available at all times.
When Alt+D is pressed, a menu box appears that allows for:
• a place to enter a description od the issue
• a checkbox to indicate a System lockup
• a chioce to Export a pre-formateed CD-R/DVD-R or save to the Export directory D: drive (for remote viewing through
InSite)
7-4
Figure 7-1. Alt+D Dialog Box
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Screen Capture
Screen Capture
There may be times when the customer or field engineer will want to capture a presentation on the screen. This is accomplished by first saving the image(s) to the clipboard using a Print Key.
Check the function of the Print Key in the event that the customer may have made some custom settings.
If Print key is not set to Whole Screen, proceed to step 5 to record the customer’s customized settings.
Figure 7-2. Connectivity/Button screen
5. In the Destinations section, record the service that is displayed.
parameters related to the service.
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7-5
Diagnostics/Troubleshooting
Setting the Store Key to Screen Capture
If the Print Key is not set to screen capture:
1. While on the Connectivity screen, with the Button tab displayed, go to the Destinations list.
2. From the list select Copy To Dataflow. Press [>>] to add the selection to the Printflow View section.
3. Ensure that the Physical Print Buttons section for Capture
Area is set to Whole Screen, secondary Capture and No
Image Compression.
4. The Print Key should now be set up for whole screen capture, sending the screens to the image buffer
(clipboard).
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Screen Capture
Capturing a Screen
The following is a generic process to capture any screen from the scanner:
1. Navigate to and display the image/screen to be captured.
“clipboard” displayed at the bottom of the scan image display.
Figure 7-3. Select Image to Capture
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Diagnostics/Troubleshooting
Capturing a Screen (continued)
3. Select and highlight the snapshot to be stored.
4. Select Save As Icon on the right side of the image screen.
Figure 7-4. Save As Icon
5. A Save dialog box will be opened. Choose the archive location to save image on the USB Drive or CD/DVD.
7-8
NOTE:
Figure 7-5. Save Dialog Box
It is better to save the image in Jpeg format. Image of this format can be easily reviewed in the computer.
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Screen Capture
Reset the Store Key to Customer’s Functionality
If the customer had programmed the Store Key to a function other than screen capture, restore that functionality recorded in section ‘Setting the Store Key to Screen Capture’ on page 7-6.
Refer to Figure 7-2 on page 7-5.
5, See ‘Setting the Store Key to Screen Capture’ on
page 7-6.
related to the service recorded in step 6, see ‘Setting the
Store Key to Screen Capture’ on page 7-6.
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Diagnostics/Troubleshooting
Common Diagnostics
Utilities
Provides two selections:
•
Disruptive Mode
Allows you to enable or disable disruptive mode troubleshooting.
•
System Shutdown
Allows for system shutdown from the diagnostic menu.
Select to Restart System or Shutdown System. Also, select to retain Disruptive Mode or Not.
After submitting to restart or shutdown a confirmation screen gives one last chance to confirm or cancel the request.
Remote access
Remote access is a feature designed to enable OLE’s access to customer’s desktop remotely, service engineers don’t have to be on site to connect the physical dongle to exit to desktop, it’s doable remotely by using this feature.
1. In the server side, select the system which the OLE would remotely connect to, and select Connect to device.
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Figure 7-6. Connect to device
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Utilities (continued)
connected to the system.
Common Diagnostics
Figure 7-7. Remotely Connect
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Diagnostics/Troubleshooting
Utilities (continued)
select Yes.
Figure 7-8. Enable Disruptive Mode
Figure 7-9. Diagnostic Application Area
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Common Diagnostics
Utilities (continued)
4. If we want to see the Scan screen or have control of the unit, we have to go to Virtual Console Observation and Start it.
Then connect using VNC.
Figure 7-10. Virtual Console Observation
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Diagnostics/Troubleshooting
Utilities (continued)
connected to the system.
Figure 7-11. Virtual Console Observation Connect
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Common Diagnostics
Service Diagnostics
MST
• GFW Swept Demodulator Test: performs a signal path test of the swept demodulator FPGA on the GFW.
• GFW Front-End Interface Test: tests that the GFW can access Front-End boards.
• GFS Memory Access Test: tests that GFW can access to the internal, external, external cache memory spaces.
• Front End Interface FPGA Test: reads the version of the
GFE FPGA.
• GFW Fixed Demo Test: GFW Fixed Demodulator signal path test.
• DSP Master Clock Test: tests DSP Master Clock.
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Diagnostics/Troubleshooting
Service Diagnostics (continued)
System
• MST Temperature Test.
• CPU Temperature Test.
• FPGA Version Test.
• HV_STOP Test: tests HV-STOP mechanism and checks each board is able to assert HV_STOP using its HV_STOP source.
Memory
NOTE:
• Callisto Memory Test.
The Callisto Memory test may fail if it is performed with other tests at the same time.
AnalogReceive
• BF Analog Rx Gain (High)
• BF Analog Rx Gain (Med)
• BF Analog Rx Gain (Low)
AnalogCW
• aCW IQ Symmetry Test
• aCW IQ Symmetry test
Digital Receive
• AFE Test
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Doppler Tests
Common Diagnostics
• Doppler Audio Test runs the tests for Doppler.
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Diagnostics/Troubleshooting
Service Diagnostics (continued)
PC
• Essential Test tests: PCI, PCI Express, CPU, Memory, HD
Disk and Video, CMOS, Network.
• Hard Drive Long: tests functionality of the hard drive.
• Hard Drive Short: tests functionality of the hard drive.
• Memory: tests the memory on the mother board.
• Network Adapter: Network calbe must be connected.
• System board: tests the real time clock and CMOS.
• Video: tests functionality of video adapters.
PC Interactive
•
AVI playback tests playing back an AVI file.
• Click “Play” to run the test. If the test is successful, you will see a brief video clipo with audio. For more information about the test, click “More Information”.
• Click “Pass” if the test successfully reproduces the video clip.
• Click “Fail” if the test is unable to successfully reproduce the video clip.
• Click “Cancel” button to quit the test without recording a test result.
•
Keyboard
• Press each key on the keyboard and it will be added to the History. Hold down a key to test the repeat of that key. To cancel, click Cancel or press Alt-X.
• Special purpose keys like volume control or Internet access keys may not be detected. To test the Fn key of a notebook computer, hold down the Fn key while pressing another key.
• Note: This diagnostic is intended to verify keyboard keys are in good working order. It is not intended to veriy that keyboards produce desired characters.
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Common Diagnostics
PC Interactive (continued)
•
Monitor
• This test is composed of various elements that verify a monitor functions correctly. To test a monitor feature, click the appropriate button. You can return to this dalog by clicking the mouse button or pressing any key.
• The Combination Test helps you verify your monitor is properly aligned, and set at the correct color depth and resolution. Use the crosshair pattern in each corner of the screen to visually determine if the monitor aligns correctly. If the crosshairs appear distored or out of focus, a problem may exist with the monitor alignment.
Use the color spectrum array for visually verifying the monitor color depth capacity. If the colors in the color spectrum do no blend smoothly together, a problem may exist with the monitor color depth. Use the graduated horizontal and vertical alignment bars to determine the monitor resolution capabilities. The better you can discern individual lines as they move closer together, the higher the resolution capabilities of the monitor.
• The Solid Color Test helps point out malfunctioning or dysfunctional pixels using five basic colors: red, green, blue, black, and white. Fill the screen with an appropriate color by clicking the associated button. If a pixedl is malfunctioning, the pixel color will contrast with the color of all other pixels.
• The VESA Test Patterns allow you to test the monitor for proper luminance, geometry and focus. Click the appropriate button to fill the screen with the associated test pattern. You can return to this dalog by clicking the mouse button or pressing any key.
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Diagnostics/Troubleshooting
PC Interactive (continued)
•
Trackball
• The Mouse Status Test verifies the cursor position and mouse button state. When a mouse button is pressed, the corresponding button on the picture will change color. If the mouse is a wheel or scroll mouse, an arrow will indcate the direction the wheel is being rotated.
Clicking the wheel will flash the picture of the mouse in the Mouse Status Test area.
• The Drag and Drop Test verifies a mouse can successfully perform drag and drop operations. Left click the picture of the CD and drag is onto the picture of the drive. If successful, the picture will change.
• The Double Click Test verifies a mouse can successfully perform double-click operations. Double-click on the picture of the monitor. If successful, the picture will change.
•
Sound generates sounds for testing the speakers.
•
USB Ports lists USB Devices.
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Common Diagnostics
Assessment Utility
CAUTION
Probe Assessment
1. Place the probe’s carrying case on a stable surface and open the case.
2. Carefully remove the probe and unwrap the probe cord.
3. Put the probe in the probe holder.
DO NOT allow the probe head to hang free. Impact to the probe head could result in irreparable damage.
4. Align the connector with the probe port and carefully push into place.
5. Lock the probe latch upward.
6. Carefully position the probe cord so it is free to move and is not resting on the floor.
7. Enter global service user interface as GE service.
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Diagnostics/Troubleshooting
Assessment Utility (continued)
Utility-> Probe Assessment to check the probe.
If there is no broken element and the probe is acceptable for diagnostic, the following result window displays.
Figure 7-12. Probe Assessment Pass
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Common Diagnostics
Assessment Utility (continued)
If there are broken elements and the probe is not acceptable for diagnostic. The assessment is fail and the failed elements are shown in the graphic.
CAUTION
Figure 7-13. Probe Assessment Fail
9.
Reboot the system after the probe assessment.
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Diagnostics/Troubleshooting
Probe Pass/Fail Criteria
Pass
• No dead element
• Dead elements on the edge (#0, #1 or #end-1, #end)
Fail
• Max 2 weak elemets on the scan line: -3dB<elements<-2dB
• Any one of the elements in one scan line: element<-3dB
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OP Panel Interface
Common Diagnostics
Figure 7-14. OP Panel Test
Restart the system after diagnostics
Always shutdown the system and reboot after a diagnostics session.
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Diagnostics/Troubleshooting
Network Configuration
Wire-LAN Network
1. Connect system with network.
window, check Enable DHCP, and select the proper network speed in Network Speed.
Figure 7-15. Enable DHCP
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Network Configuration
Wire-LAN Network (continued)
NOTE: If the user wants to set up static IP address, uncheck
Enable DHCP option, input static address in IP-address,
Subnet Mask and Default Gateway box. In Network
Speed box, choose the proper speed available.
Figure 7-16. Input Static IP restart the system and activate the changes.
Figure 7-17. System Restart inquiry dialog
4. The network icon at the bottom of the the screen displays as connected.
Figure 7-18. Network Icon
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Diagnostics/Troubleshooting
Wireless-LAN Network
NOTE: To configure the Wireless-LAN network, the operator must login as administrator.
1. Connect the wireless adapter in the USB port.
Wireless Network, select Configuration.
Figure 7-19. Wireless Network Settings
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Chapter 8
Replacement Procedures
This chapter describes how to remove and install, or replace, modules and subsystems in the LOGIQ V2/
LOGIQ V1. It also includes instructions for installing and re-installing the software.
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Replacement Procedures
Overview
Contents in this chapter
• ‘Warnings and important information’ on
page 8-3
• ‘Loading the software’ on
page 8-8
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Warnings and important information
Warnings and important information
Warnings
WARNING
WARNING
WARNING
Energy Control and Power Lockout for LOGIQ V2/LOGIQ V1.
When servicing parts of the Ultrasound system where there is exposure to voltage greater than 30 volts:
1. Follow LOCK OUT/TAG OUT procedures.
2. Turn off the breaker.
3. Unplug the Ultrasound system.
4. Maintain control of the Ultrasound system power plug.
5. Wait for at least 30 seconds for capacitors to discharge as there are no test points to verify isolation.
Ultrasound System components may be energized.
Because of the limited access to cabinets and equipment in the field, placing people in awkward positions, GE has limited the lifting weight for one person in the field to 16 KG (35 LBS).
Anything over 16 KG (35 LBS) requires 2 people.
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.
NOTE: Use an ESD compatible work space or the ESD-kit during parts replacement.
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Replacement Procedures
Warnings (continued)
WARNING
The waste of electrical and electronic equipment must not be disposed as unsorted municipal waste and must be collected separately.
Please contact the manufacturer or other authorized disposal company to decommission your equipment.
Returning/shipping probes and repair parts
Equipment being returned must be clean and free of blood and other infectious substances.
GE policy states that body fluids must be properly removed from any part or equipment prior to shipment. GE employees, as well as customers, are responsible for ensuring that parts/equipment have been properly decontaminated prior to shipment. Under no circumstance should a part or equipment with visible body fluids be taken or shipped from a clinic or site (for example, body coils or an ultrasound probe). The purpose of the regulation is to protect employees in the transportation industry, as well as the people who will receive or open this package.
NOTE: The US Department of Transportation (DOT) has ruled that
“items that were saturated and/or dripping with human blood that are now caked with dried blood; or which were used or intended for use in patient care” are “regulated medical waste” for transportation purposes and must be transported as a hazardous material.
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Disassembly/Re-assembly
Disassembly/Re-assembly
Warning and Caution
WARNING
ONLY QUALIFIED SERVICE PERSONNEL SHOULD
REMOVE ANY COVERS OR PANELS. ELECTRICAL
HAZARDS EXISTS AT SEVERAL POINTS INSIDE.
BECOME THOROUGHLY FAMILIAR WITH ALL
HAZARDOUS VOLTAGES AND HIGH CURRENT
LEVELS TO AVOID ACCIDENTAL CONTACT
CAUTION
Do not wear the ESD wrist strap when you work on live circuits and more than 30V peak is present.
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8-5
Replacement Procedures
Tools needed for servicing LOGIQ V2/LOGIQ V1
Table 8-1: Standard tools list for LOGIQ V2/LOGIQ V1
12
13
14
15
16
10
11
8
9
17
18
19
20
6
7
4
5
No
1
2
3 screw screw screw screw screw screw screw screw screw screw screw screw screw
Part
Name
screw screw screw screw screw screw screw
Part No.
2159632
2159634
2327793
2373562
5138465
5176890
5244775
20
34
5
14
17
4
246
12
2
1
2
2
4
5342274
5439265
5445720
2337572
5476381
5476387
5476394
5476438
5476440
5477579
5490719
5491747
5491847
6
2
3
10
QTY
2
4
135
Screw Description
Screw BH M4x6
Screw BH M4x10 WHT
D2 Screw SJ2836-87
M3x8
Screw M4x10
Screw FH M2.5x5(NL)
Screw DIN965A M4x8
Screw GB T820-2000
M3x8
Inch SScrew #6-32UNC
Screw-M4x10
GB 818-2000 M4x30
Screw FH M3x6
Bolt M8x18 with Washer
Bolt M6x15 with Washer
Bolt M8x30
Bolt M8x36 With Washer
Bolt M6x24 With Washer
Screw_DIN912 M6_20
Screw PM SW4x8
Screw Pan Head M4x4
Hand Screw M2p5x5
Screwdriver Description
Common Phillips Screwdriver
Common Phillips Screwdriver
Common Phillips Screwdriver
Common Phillips Screwdriver
Common Phillips Screwdriver
Small Phillips Screwdriver
Common Phillips Screwdriver
Common Phillips Screwdriver
Common Phillips Screwdriver
Common Phillips Screwdriver
Common Phillips Screwdriver
6# Inner Hexangular Set
5# Inner Hexangular Set
6# Inner Hexangular Set
6# Inner Hexangular Set
5# Inner Hexangular Set
5# Inner Hexangular Set
Common Phillips Screwdriver
Common Phillips Screwdriver by hand
NOTE: Please use the correct Screwdrivers listed in Table 8-1
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Disassembly/Re-assembly
Trackball Roller Cleaning
1. Rotate the retainer counterclockwise until it can be removed from the keyboard.
CAUTION
Figure 8-1. Rotate the retainer
2. Seperate the trackball and the retainer. Wipe off any oil or dust from the trackball, retainer and the trackball housing using a cleaner or cotton swab.
3. Assemble the trackball and retainer, then put in into the housing and rotate it clockwise until its notches are set in position.
When cleaning, make sure not to spill or spray any liquid into the trackball housing (keyboard or system).
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8-7
Replacement Procedures
Loading the software
Purpose of this section
This section describes how to reinstall software on
LOGIQ V2/LOGIQ V1.
Customer provided prerequisite
• Formatted and labelled media for Images storage.
• Formatted and labelled media for Patient Archive and
Presets (User Defined Settings).
• Password for the user ADM.
Data Management - moving all images
CAUTION
An error, or a power loss may occur.
Always backup the Patient Archive and the Presets (System
Configurations) before loading the software!
In order to complete a successful restore of the Patient
Database, as needed after a hard disk replacement, or if all the content on the hard disk has been erased, the images must be moved away from LOGIQ V2/LOGIQ V1 before doing backup of the Patient Database.
Depending on the location set-up, either move the images to a remote server or to removable media like DVD or CD discs.
• Move the images to a remote server or to removable media.
For instructions, please see “Disk management” in the User
Manual/User Guide.
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Loading the software
Backing up the Patient Archive and System Configurations
CAUTION
An error, or a power loss may occur.
Always backup the Patient Archive and the Presets (System
Configurations) before loading the software!
In order to complete a successful restore of the Patient
Database, as needed after a hard disk replacement, or if all the content on the hard disk has been erased, the images must be moved away from LOGIQ V2/LOGIQ V1 before doing backup of the Patient Database.
Depending on the location set-up, either move the images to a remote server or to removable media like DVD or CD discs.
• Backup the Patient Archive and System Configurations.
For instructions, please see “Data Backup and Restore” in the User Manual/User Guide.
Recording important settings and parameters
Overview
CAUTION
An error, or a power loss may occur.
It is considered to be best practice to always keep a record on paper of the settings for the LOGIQ V2/LOGIQ V1. Verify if it is current before you start to load software!
Always keep a record of the settings for the LOGIQ V2/LOGIQ
V1 on paper. Verify if it is current before starting a software loading! If needed, record the settings.
This subsection includes descriptions for recording data from the following screens:
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Replacement Procedures
Loading the System Software
WARNING
While the software install procedure is designed to preserved data, you should save any patient data, images, system setups and customer presets to CD,
DVD, USB Flash Drive, or USB Hard Disk before doing a software upgrade.
NOTE: Before loading the system software, please ensure that the power can be continuously supplied and there is no risk of power cut off during loading procedure.
There are two methods to load the system software:
• Load the system software with USB memory stick.
• Load the system software with SD Card.
Loading the System Software with USB memory stick
NOTE: Before starting this procedure, remove all probes and peripherals and remove them from the Docking Cart.
NOTE: While it is believed to be unnecessary, it would not hurt to disconnect the system from the network and remove all transducer.
NOTE: Please ensure AC adapter is connected during system upgrade!
NOTE:
1. Insert the USB memory stick labeled “System & Application
Software” to the system.
2. Properly turn off the scanner by momentarily pressing the
Power On/Off Switch. In System-Exit window, select
Shutdown to shutdown the system.
If the system will not shutdown normally, hold down the
Power On/Off Switch until the light turns off.
3. Power on the system. The system will detect the USB memory stick automatically.
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Loading the software
Loading the System Software with USB memory stick (continued)
4. Select one of the options and then press Enter key to continue. Select choice [1] to load the C disk only.
NOTE:
Figure 8-2. System Software load instruction
• To select [1], only the bootable C: partition is loaded.
This option is intended for recovery of a system that will not boot up.
When to select [1] to load C disk, please ensure that any patient data on the disk has been backed up.
CAUTION
If you select [1], ALL existing software and data will be erased.
If backup has not been performed, all data like Patient
Database, System Configuration and User Configurations
(Customer Presets) will be lost.
• To select [2], wipe tool <service only>: This option is used by service engineer only to wipe all the patient data.
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Replacement Procedures
Loading the System Software with USB memory stick (continued)
NOTE: All the patient data cannot be recovered after wipe process.
• To select [3], Service tool. The complete disk will be loaded. This option is recommended for application software upgrade.
WARNING
WARNING
While the software install procedure is designed to preserve data, you should select choice [1] to format disk
C only.
5. System USB memory stick will be loading. Wait for the software installation to complete.
Do not interrupt the software loading at any time.
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Figure 8-3. Loading Process
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Loading the software
Loading the System Software with USB memory stick (continued)
system will shutdown automatically.
NOTE:
Figure 8-4. System upgrade complete
7. Remove the USB memory stick and then press Power On/
Off switch to power on the system.
If you do not remove the USB memory stick, the software system loading process repeats when the system boots up.
8. When the system is powered on, the system indicates to input password. The password is Service rotating
password and it is case sensitive.
Figure 8-5. Input Password
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8-13
Replacement Procedures
Wipe Tool
Wipe tool is intended to erase all the patient data with the software to wipe the partitions on the system before the system will be shipped for service.
NOTE: Wipe tool will be performed with the software USB flash drive.
Be sure your software USB flash drive is well kept.
CAUTION
The system can not be boot up after wipe process.
WARNING
The wipe procedure will erase all the patient data and all existing software on the system. While the wipe procedure is designed to preserved data, you should save any patient data, images, system setups and customer presets to CD, DVD,
USB Flash Drive, or USB Hard Disk before doing the wipe process.
NOTE: Before starting the wipe tool, please ensure that the power can be continuously supplied and there is no risk of power cut off during loading procedure.
NOTE:
1. Insert USB flash drive labeled “System & Application
Software” to the system.
2. Properly turn off the system by momentarily pressing the
Power/On/Off Switch. In System-Exit window, select
Shutdown to shutdown the system.
If the system will not shut down normally, hold down the
Power On/Off Switch until the light turns off.
3. Power on the system. The system will detect the USB flash drive automatically.
8-14 LOGIQ V2/LOGIQ V1 – Basic Service Manual
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Loading the software
Wipe Tool (continued)
NOTE:
NOTE:
4. Select [2] Wipe tool and then select Next to continue.
All patient data cannot be recovered after this operation.
Contact GE service for support.
All patient data (if any) will be destroyed! Please backup patient data before executing erasing patient data!
Figure 8-6. Upgrade USB message
5. The system indicates all data will be erased, select Yes to continue.
Figure 8-7. Confirmation Dialog
LOGIQ V2/LOGIQ V1 – Basic Service Manual
5610739-100 English Rev.3
8-15
Replacement Procedures
Wipe Tool (continued)
NOTE:
6. The software is wiping the partitions. Wait for the wipe tool procedure to complete. On the screen, it displays how much has been completed.
Do not interrupt the wipe tool process at any time until all the partitions wiping is completed.
Figure 8-8. Wiping progress will shutdown automatically.
8-16
Figure 8-9. Process Complete
LOGIQ V2/LOGIQ V1 – Basic Service Manual
5610739-100 English Rev.3
Loading the software
Wipe Tool (continued)
NOTE: As the SSD is empty after wipe process, the system cannot boot up. The software should be loaded first after the wipe process.
8. The wipe tool procedure has erased all patient data and all existing software.
NOTE: After the system is returned from service, restore the patient data, images, system setups and customer presets on your system. Contact GE service for support.
Software Version check out
Functional Check-out
1. Power on LOGIQ V2/LOGIQ V1 system and wait until system booting to main screen.
Figure 8-10. About
4. Check whether “Software Version” is the right version for use.
Figure 8-11. Software version
LOGIQ V2/LOGIQ V1 – Basic Service Manual
5610739-100 English Rev.3
8-17
Replacement Procedures
Reload the Correct Preset Region
NOTE: After the system software loading completion, please reload the correct preset region.
1. Reboot the system.
Preset Region.
Figure 8-12. Preset Region
4. Reboot the system.
8-18 LOGIQ V2/LOGIQ V1 – Basic Service Manual
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Loading the software
Option Strings Check
NOTE: After the system software loading completion, please check the option strings to ensure that the options are activated and working.
1. Reboot the system.
2. Select Utility -> Admin -> System Admin.
3. Ensure that all the installed option keys are displayed and the status of Options are valid.
• The status “Valid” means the option keys are activated and working.
• The status “disabled” means the option keys are not activated and not working. Check if the option is installed and if the serial number and option key are correct.
Option strings
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8-19
Replacement Procedures
Probe Recognition Check
NOTE: After the system software loading completion, please check to ensure that the system can recognize the probes.
Plug in the probe. In scanning mode, the probe information is displayed on the right top location of the screen. About the probe specification for intended use on LOGIQ V2/LOGIQ V1.
Plug in at least one of each type of the probes and check if each of the probes is recognized and the probe information is displayed correctly.
Figure 8-13. Probe identification
Peripheral Device Check
Check to ensure that all the peripheral devices work properly.
For instruction of peripheral device check, See ‘Peripheral checks’ on
page 4-39 for more information.
8-20 LOGIQ V2/LOGIQ V1 – Basic Service Manual
5610739-100 English Rev.3
Loading the software
Reinstall DICOM Devices
Reinstall any DICOM devices used by the customers and check to ensure these DICOM devices work properly.
The instruction about installing DICOM devices is not incorporated in this manual. To access the instruction about installing DICOM devices please refer to another manual Basic
User Manual. Please use the latest revision of this document.
LOGIQ V2/LOGIQ V1 – Basic Service Manual
5610739-100 English Rev.3
8-21
Replacement Procedures
8-22 LOGIQ V2/LOGIQ V1 – Basic Service Manual
5610739-100 English Rev.3
Chapter 9
Renewal Parts
This chapter lists the renewal parts available for the
LOGIQ V2/LOGIQ V1.
LOGIQ V2/LOGIQ V1 – Basic Service Manual
5610739-100 English Rev.3
9-1
Renewal Parts
Contents in this chapter
• List of Abbreviations
• Renewal Parts Lists
Overview
9-2 LOGIQ V2/LOGIQ V1 – Basic Service Manual
5610739-100 English Rev.3
List of Abbreviations
List of Abbreviations
Table 9-1: List of Abbreviations
ABBREVIATION
3D
Assy
DESCRIPTION
THREE DIMENSIONAL
ASSEMBLY
FRU 1
FRU 2
Replacement part available in part hub
Replacement part available from the manufacturer (lead time involved)
KBD Keyboard
LCD
BnV
TMST
Liquid Crystal Display
Brightness and Volume
Master Board
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9-3
Renewal Parts
Renewal Parts Lists
Item
005
006
007
008
001
002
003
004
009
010
011
012
AC Power Cord
Table 9-2: AC Power Cord
Part
Number
5177123-2
5176304-2
5176773-2
5177195-2
5176907-2
5177153-2
5177154-2
5177187-3
5177146-2
5400868-2
5176753-2
5177126-2
Part Name
AC Power Cord Europe
AC Power Cord China
AC Power Cord India
AC Power Cord Argentina
AC Power Cord UK
AC Power Cord Denmark
AC Power Cord Switzerland
AC Power Cord Australia
AC Power Cord USA
AC Power Cord Brazil
AC Power Cord Israel
AC Power Cord Japan
1
1
1
1
1
1
1
1
1
1
1
1
Quantity
1
1
1
1
1
1
1
1
1
1
1
1
FRU
9-4 LOGIQ V2/LOGIQ V1 – Basic Service Manual
5610739-100 English Rev.3
Operator Console Assy
Renewal Parts Lists
Figure 9-1. Operator Console Assy
LOGIQ V2/LOGIQ V1 – Basic Service Manual
5610739-100 English Rev.3
9-5
Renewal Parts
Item
700
701
702
703
704
705
Probe and Accessories
Table 9-3: Probes for LOGIQ V2/LOGIQ V1
Part Name
4C-RS
L6-12-RS
3Sc-RS
8C-RS
E8C-RS
LK760-RS
Part
Number
5451471
5454332
5433833
5434203
5499516
5548914
Center Image Frequency (MHz)
3.10
7.75
2.75
6.50
6.50
7.15
1
1
1
1
1
1
Qty
1
1
1
1
1
1
FRU
9-6 LOGIQ V2/LOGIQ V1 – Basic Service Manual
5610739-100 English Rev.3
Renewal Parts Lists
Peripheral
823
824
825
826
819
820
821
822
827
828
829
815
816
817
818
811
812
813
814
Item
808
808
809
810
830
Table 9-4: Peripherals for LOGIQ V2/LOGIQ V1
5494719
5494718
5426594
5426595
5426596
5426597
5151259-2
5151261-2
5133106-2
5133017-2
5133108-2
5133109-2
5151262
5151259
5151261
5151263
5151262-2
5151263-2
5495509-2
Part Number
5338419
5338419
5168040-4
5434317-3
5692048-3
Description
Footswitch
Footswitch FSU-1000
Footswitch MKF 2-MED USB GP26
USB Stick
Sandisk USB Stick 4G
1TB USB mobile HDD
Printer
Sony UPD25 Color Printer Chinese kit
Sony UPD25 Color Printer USA kit
Sony UPD25 Color Printer European kit
Sony UPD25 Color Printer Japanese kit
UP-D897MD B/W Printer Chinese kit
UP-D897MD B/W Printer USA kit
UP-D897MD B/W Printer European kit
UP-D897MD B/W Printer Japanese kit
Sony UP-D711MD B/W Printer with Paper Kit
Sony UP-D711MD B/W Printer Paper 1 roll
HP100 Printer Chinese kit
HP100 Printer European kit
HP100 Printer Japanese kit
HP100 Printer USA kit
UP-D898MD B/W Printer USA kit
UP-D898MD B/W Printer Europe kit
UP-D898MD B/W Printer China kit
UP-D898MD B/W Printer Japan kit
UP-D898MD B/W Printer Brazil kit
System and Application USB
LOGIQ V2/LOGIQ V1 R1.0.2 System and
Application Software USB
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
Qty
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5610739-100 English Rev.3
9-7
Renewal Parts
Item
904
905
906
907
900
901
902
903
908
909
910
911
Power Cord
Table 9-5: Power Cord for LOGIQ V2/LOGIQ V1
Part Number
5177123-2
5176304-2
5176773-2
5177195-2
5176907-2
5177153-2
5177154-2
5177187-3
5177146-2
5400868-2
5176753-2
5177126-2
Description
AC Power Cord Europe
AC Power Cord China
AC Power Cord India
AC Power Cord Argentina
AC Power Cord UK
AC Power Cord Denmark
AC Power Cord Switzerland
AC Power Cord Australia
AC Power Cord USA
AC Power Cord Brazil
AC Power Cord Israel
AC Power Cord Japan
1
1
1
1
1
1
1
1
1
1
1
1
Qty
1
1
1
1
1
1
1
1
1
1
1
1
FRU
9-8 LOGIQ V2/LOGIQ V1 – Basic Service Manual
5610739-100 English Rev.3
Renewal Parts Lists
Manuals
1004
1005
1006
1007
1008
1009
1010
1019
1020
1021
1022
1015
1016
1017
1018
1023
1024
1025
1026
1011
1012
1013
1014
Item
1000
1001
1002
1003
5610736-142
5610736-144
5610736-145
5610736-150
5610736-151
5610736-153
5610736-154
5610736-155
5610736-159
5610736-160
5610736-161
5610736-162
5610736-100
5610736-101
5610736-106
5610736-108
5610736-111
5610736-121
5610736-127
5610736-129
5610736-131
5610736-140
5610736-141
Table 9-6: Manuals for LOGIQ V2/LOGIQ V1
Part Number
5610741-200
5610738-100
5610739-100
5610735-100
Description
LOGIQ V2/LOGIQ V1 Manual CD
LOGIQ V2/LOGIQ V1 Advanced Reference Manual
LOGIQ V2/LOGIQ V1 Basic Service Manual
LOGIQ V2/LOGIQ V1 Basic User Manual English version
LOGIQ V2/LOGIQ V1 User Guide English version
LOGIQ V2/LOGIQ V1 User Guide French version
LOGIQ V2/LOGIQ V1 User Guide Spanish version
LOGIQ V2/LOGIQ V1 User Guide German version
LOGIQ V2/LOGIQ V1 User Guide Italian version
LOGIQ V2/LOGIQ V1 User Guide Dutch version
LOGIQ V2/LOGIQ V1 User Guide Brazilian Portuguese version
LOGIQ V2/LOGIQ V1 User Guide Estonian version
LOGIQ V2/LOGIQ V1 User Guide Slovenian version
LOGIQ V2/LOGIQ V1 User Guide Japanese version
LOGIQ V2/LOGIQ V1 User Guide Simplified Chinese version
LOGIQ V2/LOGIQ V1 User Guide Swedish version
LOGIQ V2/LOGIQ V1 User Guide Korean version
LOGIQ V2/LOGIQ V1 User Guide Russian version
LOGIQ V2/LOGIQ V1 User Guide Polish version
LOGIQ V2/LOGIQ V1 User Guide Greek version
LOGIQ V2/LOGIQ V1 User Guide Hungarian version
LOGIQ V2/LOGIQ V1 User Guide Slovakian version
LOGIQ V2/LOGIQ V1 User Guide Czech version
LOGIQ V2/LOGIQ V1 User Guide Turkish version
LOGIQ V2/LOGIQ V1 User Guide Danish version
LOGIQ V2/LOGIQ V1 User Guide Norwegian version
LOGIQ V2/LOGIQ V1 User Guide Finnish version
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
Qty
N
N
N
N
N
N
N
N
N
N
N
N
N
N
N
N
N
N
N
N
N
N
N
FRU
N
N
N
N
LOGIQ V2/LOGIQ V1 – Basic Service Manual
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9-9
Renewal Parts
Item
1027
1028
1029
1030
1031
1032
1033
1034
1035
5610736-181
5610736-184
Table 9-6: Manuals for LOGIQ V2/LOGIQ V1
Part Number
5610736-165
5610736-167
5610736-168
5610736-174
5610736-175
5610736-176
5610736-177
Description
LOGIQ V2/LOGIQ V1 User Guide Bulgarian version
LOGIQ V2/LOGIQ V1 User Guide Romanian version
LOGIQ V2/LOGIQ V1 User Guide Croatian version
LOGIQ V2/LOGIQ V1 User Guide Lithuanian version
LOGIQ V2/LOGIQ V1 User Guide Latvian version
LOGIQ V2/LOGIQ V1 User Guide Serbian version
LOGIQ V2/LOGIQ V1 User Guide European
Portuguese version
LOGIQ V2/LOGIQ V1 User Guide Indonesian version
LOGIQ V2/LOGIQ V1 User Guide Kazakh version
1
1
1
1
1
1
1
1
1
Qty FRU
N
N
N
N
N
N
N
N
N
9-10 LOGIQ V2/LOGIQ V1 – Basic Service Manual
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Chapter 10
Care and Maintenance
This chapter describes Care and Maintenance on the
Ultrasound system and peripherals. These procedures are intended to maintain the quality of the Ultrasound
system’s performance. Read this chapter completely and familiarize yourself with the procedures before performing a task.
LOGIQ V2/LOGIQ V1 – Basic Service Manual
5610739-100 English Rev.3
10-1
Care and Maintenance
Overview
Contents in this chapter
• ‘Why do maintenance’ on page 10-4
• ‘Maintenance task schedule’ on page 10-6
• ‘Tools required’ on page 10-8
• ‘System maintenance’ on page 10-12
• ‘Electrical safety tests’ on page 10-19
• ‘When there's too much leakage current …’ on page 10-30
• ‘Inspection Paperwork’ on page 10-32
• ‘Electrical Safety Tests Log’ on page 10-34
10-2 LOGIQ V2/LOGIQ V1 – Basic Service Manual
5610739-100 English Rev.3
Warnings
Warnings
DANGER
CAUTION
BE SURE TO DISCONNECT THE ULTRASOUND SYSTEM
POWER PLUG AND OPEN THE MAIN CIRCUIT BREAKER
BEFORE YOU REMOVE ANY PARTS. BE CAUTIOUS
WHENEVER POWER IS STILL ON AND COVERS ARE
REMOVED.
Practice good ESD prevention. Wear an anti–static strap when handling electronic parts and even when disconnecting/ connecting cables.
CAUTION
Do not pull out or insert circuit boards while power is on.
CAUTION
Do not operate this Ultrasound system unless all board covers and frame panels are securely in place. System performance and cooling require this.
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10-3
Care and Maintenance
Why do maintenance
Periodic maintenance inspections
It has been determined by engineering that your LOGIQ V2/
LOGIQ V1 does not have any high wear components that fail with use, therefore no Periodic Maintenance inspections are mandatory.
However, some customers’ Quality Assurance Programs may require additional tasks and or inspections at a different frequency than listed in this manual.
Keeping records
It is good business practice that ultrasound facilities maintain records of periodic and corrective maintenance. The Ultrasound
Periodic Maintenance Inspection Certificate provides the customer with documentation that the Ultrasound system is maintained on a periodic basis.
A copy of the Ultrasound Periodic Maintenance Inspection
Certificate should be kept in the same room or near the
Ultrasound system.
10-4 LOGIQ V2/LOGIQ V1 – Basic Service Manual
5610739-100 English Rev.3
Why do maintenance
Quality assurance
In order to gain accreditation from organizations such as the
American College of Radiology (USA), it is the customer’s responsibility to have a quality assurance program in place for each Ultrasound system. The program must be directed by a medical physicists, the supervising radiologist/physician or appropriate designee.
Routine quality control testing must occur regularly. The same tests are performed during each period so that changes can be monitored over time and effective corrective action can be taken.
Testing results, corrective action and the effects of corrective action must be documented and maintained on the site.
Your GE service representative can help you with establishing, performing and maintaining records for a quality assurance program. Contact GE for coverage and/or price for service.
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5610739-100 English Rev.3
10-5
Care and Maintenance
Maintenance task schedule
How often should maintenance tasks be performed?
The Care and Maintenance task schedule (provided in
Table 10-1 on page 10-6) specifies how often your LOGIQ V2/
LOGIQ V1 should be serviced and outlines items requiring special attention.
NOTE: It is the customer’s responsibility to ensure the LOGIQ V2/
LOGIQ V1 care and maintenance is performed as scheduled in order to retain its high level of safety, dependability and performance.
Your GE Service Representative has an in-depth knowledge of your LOGIQ V2/LOGIQ V1 and can best provide competent, efficient service. Contact GE for coverage information and/or price for service.
The service procedures and recommended intervals shown in the Care and Maintenance Task Schedule assumes that you use your LOGIQ V2/LOGIQ V1 for an average patient load
(10-12 per day) and not use it as a primary mobile Ultrasound system which is transported between diagnostic facilities.
NOTE: If conditions exist which exceed typical usage and patient load, then it is recommended to increase the periodic maintenance frequencies.
Service at Indicated
Time
Clean Probes
Inspect AC Mains Cable
Table 10-1: Customer Care Schedule
Daily Weekly
•*
Monthly
Per
Facilities
QA
Program
•
Notes
* or before each use
Mobile Ultrasound system: Check
Weekly
Inspect Cables and
Connectors
Clean Console
•
•
10-6 LOGIQ V2/LOGIQ V1 – Basic Service Manual
5610739-100 English Rev.3
Maintenance task schedule
Service at Indicated
Time
Clean LCD
Console Leakage Current
Checks
Peripheral Leakage
Current Checks
Surface Probe Leakage
Current Checks
Endocavity Probe Leakage
Current Checks
Surgical Probe Leakage
Current Checks
Measurement
Accuracy Checks
Functional Checks
Table 10-1: Customer Care Schedule (Continued)
Daily Weekly
•
Monthly
Per
Facilities
QA
Program
See Notes
See Notes
See Notes
See Notes
See Notes
See Notes
See Notes
Notes
Twice Annually
Twice Annually
Twice Annually
Quarterly Annually
Quarterly Annually
Twice Annually also after corrective maintenance
NOTE: The maintenance may require specialized equipment to complete.
NOTE: The periodic maintenances are not mandatory. The table above is for reference only.
LOGIQ V2/LOGIQ V1 – Basic Service Manual
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10-7
Care and Maintenance
Tools required
NOTE: For a list of required tools for servicing the LOGIQ V2/LOGIQ
V1, refer to chapter 8.
Standard GE tool kit
Tool ID
9-45358
9-4078
9-44572
9-44579
9-44579
9-45385
9-45378
9-4518
9-4518
9-44776
9-44601
9-4151
9-41421
9-41594
9-41581
9-39451
The following is a description of the “Standard” GE tool kit in the
USA. Not all tools are required.
Table 10-2: Overview of GE-1 tool kit contents
Description
Pliers Retaining Ring
Scribe
Wrench Open End 3/8 - 7/16
Wrench Open End 1/2 - 9/16
Wrench Open End 1/2 - 9/16
Pliers, Arc Joint 7 inch
Pliers, Slip Joint
Pliers, Long Nose, Miniature
Pliers, Long Nose, Miniature
Ignition Wrench Set, 10 pc.
Wrench, Adj., 4 inch
Screwdriver, Blade, Stubby
Screwdriver, Blade, Pocket clip
Screwdriver, Blade 1/8 in. × 4 in.
Screwdriver, Blade 3/16 in. × 4 in.
20' Steel Tape, locking Spring load
Tool ID
9-XL9971MM
9-XL9972MM
9-XL9973MM
9-XL9974MM
9-XL9975MM
9-XL9976MM
9-XL9977MM
9-XL991CM
C2356E
BLBO
DWL4283T
9-41322
9-6757
9-9487
9-45341
9-3001
Description
Xcelite-hex Blade 1.27mm
Xcelite-hex Blade 1.5mm
Xcelite-hex Blade 2 mm
Xcelite-hex Blade 2.5mm
Xcelite-hex Blade 3mm
Xcelite-hex Blade 4mm
Xcelite-hex Blade 5mm
Handle
Screw starter - Kedman
Quick Wedge
Box - 18 Compartment
Box - 5 Compartment
Pickup Tool, Claw type
6 pc Needle File Set
Utility Knife
Pliers Vice Grip 10 inch
Xacto Pen Knife
10-8 LOGIQ V2/LOGIQ V1 – Basic Service Manual
5610739-100 English Rev.3
Tools required
Tool ID
9-GH807
68-412
9-GH130
9-41584
9-4118
9-41293
9-41294
9-41295
9-46677
9-34701
9-43499
9-4355
9-43523
9-43531
9-65283
9-46696
9-39829
9-38461
9-4280
9-WEW60P3
9-WECT5B6
9-WEWDP12
93383
9-GH408
21576
Table 10-2: Overview of GE-1 tool kit contents (Continued)
Description
Ratchet, Offset, Slotted
Ratchet, Offset, Phillips
Tapered Reamer
Screwdriver, slotted 1/4 in. × 6 in.
Screwdriver, Phillips #2,
Stubby
Screwdriver, Phillips #0
Screwdriver, Phillips #1
Screwdriver, Phillips #2
Hex Keys, 20 pc., Metric
1/4 in. Standard Socket set (19 pc)
1/2 inch Socket 1/4 inch drive
Flex Spinner
Breaker
6 inch Ext.
Case 8.5 in. × 4.5 in. × 2 in.
Deep
Hex Keys
Tool ID
9-HT62002
9-4099
9-GH3001
9-GH300ME
9-XL9920
9-XL9921
9-XL9922
9-XL9923
9-XL9924
9-XL9925
9-XL9926
9-XL99764
9-XL99964
9-XLM60
9-45072
9-XL100X
Description
Solder Aid, Fork and Hook
Mirror, Round, Telescoping
Steel Rule Decimal 6 inch
Steel Rule Metric 6 inch
Xcelite-hex Blade.050 inch
Xcelite-hex Blade 1/16 inch
Xcelite-hex Blade 5/16 inch
Xcelite-hex Blade 3/32 inch
Xcelite-hex Blade 1/8 inch
Xcelite-hex Blade 5/32 inch
Xcelite-hex Blade 3/16 inch
Xcelite-hex Blade 7/64
Xcelite-hex Blade 9/64
Mini-screwdriver kit
Pliers 6 inch Diagonal
Torpedo Level, Magnetic
Hammer, Ball Peen, 4 oz.
Universal Joint 1/4 inch
Weller - Soldering Iron, 3 wire
Weller - Soldering Iron Tip
Weller - Desoldering Pump
Flashlight Mini-Mag Lite (AAA
Bat.)
Tweezers
Brush - Bristle
9-XL87CG
9-WEWDT-07
9-WS175-E
KH174
KH175
9-Z9480121
Wire Stripper/Cutter 5 inch -
100X
Pliers - very fine needle nose-87CG
Weller-Soldering-Replacem ent Tip(1)
Wiss - Surgical Scissors
Hemostat 5 inch Straight
Hemostat 5 inch curved
Alignment tool (red)
LOGIQ V2/LOGIQ V1 – Basic Service Manual
5610739-100 English Rev.3
10-9
Tool ID
9-45381
9-45092
9-42882
9-42884
9-42886
9-42973
9-GH77
9-GH890
9-31276
9-31277
9-31263
21045C
9-44604
9-41587
9-41586
9-GH19512
9-44741
Care and Maintenance
Tool ID
9-4516
Table 10-2: Overview of GE-1 tool kit contents (Continued)
Description
Pliers 4 1/4 inch Diagonal
Tool ID Description
GE-2 tool kit
Table 10-3: Overview of GE-2 tool kit contents
GE-2 Sears Kit (#99034)
Description Tool ID
Pliers, Arc Joint 9 1/2 inch 9-44067
Pliers, Linesman 8 1/2 inch
Punch, Pin 3/32 inch
Punch, Pin 5/32 inch
Punch, Pin 1/4 inch
Cold Chisel 1/2 inch
Center Punch Automatic
File Handle, Adj.
File, Round, Bastard 8 inch
File, Half Round, Bastard 8 inch
File, Flat Mill 8 inch
Close Quarter Saw
Wrench, Adj. 10 inch
Screwdriver 5/16 inch × 8 inch
Screwdriver, Stubby 5/16 inch
Countersink 1/2 inch
12 PC Combination Wrench
Set
9-42679
9-44262
9-4258
9-34374
9-44311
9-33485
9-33484
9-33484
9-52068
9-52722
9-52723
9-44046
Description
Socket 1 1/16 in. for 1/2 in. drive
Socket 10MM Hex for 1/2 in. drive (2273333)
Extension 10 inch for 1/2 in. drive (2273405)
3/8 inch to 1/2 inch Adapter
3/8 inch Metric Socket Set -
12 PT
16mm Socket 12 pt.
Metal Socket Tray
Metal Socket Tray
Metal Socket Tray
Tap and Drill Set
#6 Tap
#8 Tap
High Speed Drill Set
#36 Drill
#29 Drill
3/8 inch Socket Set
10-10 LOGIQ V2/LOGIQ V1 – Basic Service Manual
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Tools required
Special tools, supplies and equipment used for maintenance
Table 10-4: Overview of tool requirements for periodic maintenance
Tool / kit
Digital Volt Meter (DVM)
Anti Static Kit
Comments
Anti Static Vacuum Cleaner
Safety Analyzer
QIQ Phantom
B/W Printer Cleaning Sheet
Color Printer Cleaning Sheet
Disposable Gloves
Kit includes anti–static mat, wrist strap and cables for 200 to 240V system
3M #2204 Large adjustable wrist strap
3M #2214 Small adjustable wrist strap
3M #3051 conductive ground cord
120V
230V
The safety Analyzer tool should be calibrated and compliant with AAMI/ESI 1993 or IEC 60601 or
AS/NZS 3551.
RMI Grayscale Target Model 403GS
NOTE! The use of a Phantom is not required during Preventive Maintenance. Customer may use it as part of their Quality Assurance
Program tests.
See printer user manual for requirements
See printer user manual for requirements
LOGIQ V2/LOGIQ V1 – Basic Service Manual
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10-11
Care and Maintenance
System maintenance
Preliminary checks
The preliminary checks take about 15 minutes to perform. Refer to the Ultrasound system user documentation whenever necessary.
Table 10-5: System preliminary checks
Step Item Description
1.
2.
3.
4.
5.
6.
Ask and Listen
Paperwork
Power up
Probes
Displays
InSite
Ask the customer if they have any problems or questions about the equipment.
Fill in the top of Ultrasound Inspection Certificate (see Figure 10-5 on
page 10-32). Record all probes and Ultrasound system options.
• Turn the Ultrasound system power on and verify that all fans and peripherals turn on.
• Watch the displays during power up to verify that no warning or error messages are displayed.
• Where applicable, confirm that the battery is charged. If no AC Input present, use the internal battery.
Verify that the Ultrasound system properly recognizes all probes.
Verify proper display on the monitor.
Where applicable, for Warranty and Contract Customers only:
• Verify that InSite is functioning properly.
• Ensure two-way remote communications.
7. Review Error Logs Where applicable, Error Logs can be reviewed via system diagnostics.
8. Diagnostics Optional.
9.
10.
Presets
Image Archive
Backup all Customer Presets to an appropriate media.
Back up the Image Archive onto appropriate media.
10-12 LOGIQ V2/LOGIQ V1 – Basic Service Manual
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System maintenance
Functional checks
NOTE: See also Chapter 4
The functional checks take about 60 minutes to perform. Refer to the Ultrasound system user documentation whenever necessary.
System checks
Table 10-6: System functional checks
Step
1.
2.
3.
4.
5.
Item
B-Mode
CF-Mode
Doppler Modes
M-Mode
Probe Elements
6. Applicable
Software Options
7. Xmit/Recv
Elements
Description
Verify basic B-Mode operation. Check the basic Ultrasound system controls that affect this mode of operation.
Verify basic CF-Mode (Color Flow Mode) operation. Check the basic
Ultrasound system controls that affect this mode of operation.
Verify basic Doppler operation (PW and CW if available). Check the basic
Ultrasound system controls that affect this mode of operation.
Verify basic M-Mode operation. Check the basic Ultrasound system controls that affect this mode of operation.
Perform an Element Test on each probe to verify that all the probe elements and system channels are functional.
Verify the basic operation of all optional modes such as Contrast. Check the basic Ultrasound system controls that affect each options operation.
Use the Visual Channel Utility on the loop connect to verify that all system xmit/recv channels are functional.
9.
10.
12.
13. test
Keyboard
LCD
Do the interactive keyboard test.
Verify basic LCD display functions. Refer to Chapter 3 of the User Manual.
Menu Verify Software Menu display functions. Refer to Chapter 3 of the User check
Peripherals
Manual.
See: ‘Peripheral checks’ on page 4-39.
Measurements In measurement mode, make distance measurement, get result in result window. Verify the distance by graduate rule. Distance Accuracy should be within
±5%. (Name result from result window Result A, result from graduate rule Result B; Distance Accuracy = (Result B-Result A)/Result A)
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10-13
Care and Maintenance
Peripheral/option checks
Step
1.
2.
3.
4.
5.
6.
If any peripherals or options are not part of the system configuration, the check can be omitted.
Refer to the User Manual for a list of approved peripherals/ options.
Table 10-7: GE approved peripheral/hardware option functional checks
Item
Media
B/W Printer
Color Printer
DICOM
Footswitch
DVD
Description
Verify media drive(s) read/write properlty. Clean if necessary.
Verify hardcopy output of the B/W video page printer. Clean heads and covers if necessary.
Verify hardcopy output of the Color video page printer. Clean heads and covers if necessary.
Verify that DICOM is functioning properly. Send an image to a DICOM device.
Verify that the footswitch is functioning as programed. Clean as necessary.
Verify that the DVD is functioning properly. Clean heads and covers if necessary.
Mains cable inspection
Table 10-8: Mains Cable Inspection, As Appropriate
Step
1.
2.
3.
Item
Unplug Cord
Inspect
Verify
Description
Disconnect the mains cable from the wall and Ultrasound system.
Inspect it and its connectors for damage of any kinds.
Verify that the LINE, NEUTRAL and GROUND wires are properly attached to the terminals, and that no strands may cause a short circuit.
10-14 LOGIQ V2/LOGIQ V1 – Basic Service Manual
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System maintenance
Cleaning
Step
1.
Item
Console
2.
3.
Probe Holder
LCD
Table 10-9: General Cleaning
Description
Remove the battery. Use a fluid detergent in warm water on a soft, damp cloth to carefully wipe the entire system. Be careful not to get the cloth too wet so that moisture does not enter the console.
Clean probe holders. (they may need to be soaked to remove excess gel).
Use a soft, non-abrasive folder cloth. Gently wipe the LCD face. DO NOT use a glass cleaner that has a hydrocarbon base (such as Benzene,
Methy Alcohol or Methy Ethyl Ketone) on LCD with the filter (anti-glare shield).
Physical inspection
Step
1.
2.
3.
6.
8.
NOTE: These features may not be present on all Ultrasound systems.
Table 10-10: Physical checks
Item Description
Labeling Verify that all Ultrasound system labeling is present and in readable condition.
Scratches & Dents Inspect the exterior for dents, scratches or cracks. .
Input Power Refer to: ‘Mains cable inspection’ on page 10-14.
Connectors
Covers
Check all internal cable harnesses and connectors for wear and secure connector seating. Pay special attention to footswitch assembly and probe strain or bend reliefs.
Check to ensure that all EMI shielding, internal covers, air flow panels and screws are in place. Missing covers and hardware could cause EMI/RFI problems while scanning.
Control Panel Inspect keyboard and control panel. Note any damaged or missing items.
Lighting
Panel Check for proper operation of all operator panel and Freeze Key light.
LCD Inspect the LCD Display for scratches and bad pixels.
Verify proper operation of Contrast and Brightness controls.
Where applicable, confirm that the LCD arm allows:
• swivelling the screen to the left and to the right
• folding the screen to the locked position
• release and adjustment backwards and forwards
• can be adjusted in the up/down positions.
Note: LCD Arm movement may vary and is not applicable to all Ultrasound systems.
LOGIQ V2/LOGIQ V1 – Basic Service Manual
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10-15
Care and Maintenance
Step
11.
Item
System Status
Indicators
Battery
Table 10-10: Physical checks (Continued)
Description
Check for proper operation of all Power and System Status Indicators.
Where applicable, check that the battery is not damaged, does not leak, does not emit an odor, and is not deformed or discolored. Observe all warnings and cautions for battery handling, recharging, storing, and/or disposal,
Optional Diagnostic Checks
Optionally you can access the diagnostic software as described in Chapter 5 or 7. View the error logs and run desired diagnostics.
View the Log
1. Review the system error log for any problems.
2. Check the temperature log to see if there are any trends that could cause problems in the future.
3. Check the Configuration Log; update if needed.
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System maintenance
Probe maintenance
Probe related checks
Step
1.
2.
3.
Item
Probe Holder
Probes
Probes
Table 10-11: System preliminary checks
Description
Clean probe holders. (they may need to be soaked to remove excess gel).
Thoroughly check the Ultrasound system probe connectors and remove dust from inside the connector sockets if necessary. Visually check for bent, damaged or missing pins.
Verify that the Ultrasound system properly recognizes all probes.
Basic probe care
The Ultrasound system user manuals and various probe handling cards provide a complete description of probe care, maintenance, cleaning and disinfection. Ensure that you are completely familiar with the proper care of GE probes.
Ultrasound probes can be easily damaged by improper handling. See the User Manual and probe care cards for more details. Failure to follow these precautions can result in serious injury and equipment damage. Failure to properly handle or maintain a probe may also void its warranty.
Any evidence of wear indicates the probe cannot be used.
Do a visual check of the probe pins and Ultrasound system sockets before plugging in a probe.
The Interoperative probes often have special considerations and individual probe user manuals. For Interoperative probes also refer to their separate user manuals.
LOGIQ V2/LOGIQ V1 – Basic Service Manual
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10-17
Care and Maintenance
Basic probe cleaning
Refer to the User’s Manual for details on probe cleaning.
WARNING
To help protect yourself from blood borne diseases, wear approved disposable gloves. These are made of nitrile derived from vegetable starch to prevent allergic latex reactions.
CAUTION
CAUTION
Failure to follow the prescribed cleaning or disinfection procedures will void the probe’s warranty.
DO NOT soak or wipe the lens with any product not listed in the
User Manual. Doing so could result in irreparable damage to the probe.
Follow care instructions that came with the probe.
Disinfect a defective probe before you return it. Be sure to tag the probe as being disinfected.
10-18 LOGIQ V2/LOGIQ V1 – Basic Service Manual
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Electrical safety tests
Electrical safety tests
Safety test overview
The electrical safety tests in this section are based on and conform to IEC 60601-1 Medical Equipment Safety Standards.
They are intended for the electrical safety evaluation of cord-connected, electrically operated, patient care equipment. If additional information is needed, refer to the IEC 60601-1 documents
WARNING
THE USER MUST ENSURE THAT THE SAFETY
INSPECTIONS ARE PERFORMED AT LEAST EVERY 6
MONTHS ACCORDING TO THE REQUIREMENTS OF
THE PATIENT SAFETY STANDARD IEC-EN 60601-1.
ONLY TRAINED PERSONS ARE ALLOWED TO
PERFORM THE SAFETY INSPECTIONS MENTIONED
ABOVE.
DANGER TO MINIMIZE RISK OF ELECTRICAL SHOCK, ONLY
TRAINED PERSONS ARE ALLOWED TO PERFORM THE
ELECTRICAL SAFETY INSPECTIONS AND TESTS.
DANGER TO AVOID ELECTRICAL SHOCK, THE ULTRASOUND
SYSTEM UNDER TEST MUST NOT BE CONNECTED TO
OTHER ELECTRICAL EQUIPMENT. REMOVE ALL
INTERCONNECTING CABLES AND WIRES. THE
ULTRASOUND SYSTEM UNDER TEST MUST NOT BE
CONTACTED BY USERS OR PATIENTS WHILE
PERFORMING THESE TESTS.
CAUTION
Possible risk of infection. Do not handle soiled or contaminated probes and other components that have been in patient contact. Follow appropriate cleaning and disinfecting procedures before handling the equipment.
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10-19
Care and Maintenance
Safety test overview (continued)
Prior to initiating any electrical test, the Ultrasound system must be visually inspected. Perform the following visual checks:
• Check for missing or loose enclosure covers that could allow access to internal live parts.
• Examine the mains cord, mains plug and appliance inlet for damaged insulation and adequacy of strain relief and cable clamps.
• Locate and examine all associated transducers. Inspect the cables and strain relief at each end. Inspect the transducer enclosure and lens for cracks, holes and similar defects.
Test the system, peripherals and probes for leakage current.
Excessive leakage current can cause injury or death in sensitive patients. High leakage current can also indicate degradation of insulation and a potential for electrical failure. Do not use probes or equipment having excessive leakage current.
To minimize the risk that a probe may shock someone the customer should:
• Not use a probe that is cracked or damaged in any way.
• Check probe leakage current:
• Based on your facilities QA program for surface probes.
• Based on your facilities QA program for endocavitary probes.
• whenever probe damage is suspected.
10-20 LOGIQ V2/LOGIQ V1 – Basic Service Manual
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Electrical safety tests
Leakage current limits
WARNING
Energy Control and Power Lockout for LOGIQ V2/LOGIQ V1.
When servicing parts of the Ultrasound system where there is exposure to voltage greater than 30 volts:
1. Follow LOCK OUT/TAG OUT procedures.
2. Turn off the breaker.
3. Unplug the Ultrasound system.
4. Maintain control of the Ultrasound system power plug.
5. Wait for at least 30 seconds for capacitors to discharge as there are no test points to verify isolation.
Ultrasound System components may be energized.
CAUTION
Compare all safety-test results with safety-test results of previously performed safety tests (e.g. last year etc). In case of unexplainable abrupt changes of safety-test results consult experienced authorized service personnel or GE for further analysis.
The following limits are summarized for IEC 60601-1 Medical
Equipment Safety Standards. These limits are GEMS standards and in some cases are lower than the above standards listed.
Table 10-12: Chassis Leakage Current Limits - Accessible Metal Surface
Country
All (Except USA &
Canada)
USA & Canada
Normal
Condition
0.1 mA
0.1 mA
Open Ground
0.5 mA
0.3 mA
Reverse
Polarity
0.5 mA
0.3 mA
Open Neutral
0.5 mA
0.3 mA
All
Table 10-13: Type BF Applied Part Leakage Current Limits - Probes Surface
Country
Normal
Condition
0.1 mA
Open
Ground
0.5 mA
Reverse
Polarity
0.5 mA
Open
Neutral
0.5 mA
*Mains
Applied
5.0 mA
LOGIQ V2/LOGIQ V1 – Basic Service Manual
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10-21
Care and Maintenance
Leakage current limits (continued)
All
Table 10-14: Type CF Applied Part Leakage Current Limits - ECG Connections
Country
Normal
Condition
0.1 mA
Open
Ground
0.5 mA
Reverse
Polarity
0.5 mA
Open
Neutral
0.5 mA
*Mains
Applied
5.0 mA
NOTE: *Mains Applied refers to the sink leakage test where mains
(supply) voltage is applied to the part to determine the amount of current that will pass (or sink) to ground if a patient contacted mains voltage.
The following tests are performed at the factory and should be performed at the site. These tests are: chassis leakage current, and probe leakage current. All measurements are made with an electrical safety analyzer which should be calibrated and compliant with AAMI/ESI 1993 or IEC 60601 or AS/NZS 3551.
Table 10-15: Equipment Type and Test Definitions
Applied
Parts
(AP)
Parts or accessories that contact the patient to perform their function. For ultrasound equipment, this includes transducers and ECG leads.
Type BF Body Floating or non-conductive ultrasound probes which are marked with the 'man in box' BF symbol. this includes all transducers.
Type CF Cardiac Floating or non-conductive intraoperative probes for direct cardiac contact and isolated ECG connections so marked with the 'heart in box' CF symbol.
Sink
Leakage
The current resulting from the application of mains voltage to the applied part. This test is required test for Type CF applied parts.
10-22 LOGIQ V2/LOGIQ V1 – Basic Service Manual
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Electrical safety tests
Outlet test - wiring arrangement
Test all outlets in the area for proper grounding and wiring arrangement by plugging in the neon outlet tester and noting the combination of lights that are illuminated. Any problems found should be reported to the hospital immediately and the receptacle should not be used.
CORRECT WIRING OPEN GROUND WIRE
REVERSED POLARITY OPEN NEUTRAL WIRE
HOT AND GROUND
REVERSED
OPEN HOT WIRE
Figure 10-1. Typical alternate outlet tester
NOTE: No outlet tester can detect the condition where the Neutral
(grounded supply) conductor and the Grounding (protective earth) conductor are reversed. If later tests indicate high leakage currents, this should be suspected as a possible cause and the outlet wiring should be visually inspected.
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10-23
Care and Maintenance
Grounding continuity
DANGER ELECTRIC SHOCK HAZARD. THE PATIENT MUST NOT BE
CONTACTED TO THE EQUIPMENT DURING THIS TEST.
Measure the resistance from the third pin of the attachment plug to the exposed metal parts of the case. The ground wire resistance should be less than 0.2 ohms. Reference the procedure in the IEC60601-1.
2. OHMMETER
3. LOGIQ V2/LOGIQ V1
4. ACCESSIBLE METAL PART:
• MONITOR HOUSING
• PEAR PANEL CONNECTOR
• ANY CASTER/WHEEL SUPPORT
Figure 10-2. Ground continuity test
10-24 LOGIQ V2/LOGIQ V1 – Basic Service Manual
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Electrical safety tests
Chassis leakage current test
DANGER ELECTRIC SHOCK HAZARD. WHEN THE METER'S
GROUND SWITCH IS OPEN, DON'T TOUCH THE
ULTRASOUND SYSTEM!.
CAUTION
Equipment damage possibility. Never switch the Polarity and the status of Neutral when the Ultrasound system is powered
ON. Be sure to turn the Ultrasound system power OFF before switching them using the POLARITY switch and/or the
NEUTRAL switch. Otherwise, the Ultrasound system may be damaged.
Generic procedure
The test verifies the isolation of the power line from the chassis.
The testing meter is connected from accessible metal parts of the case to ground. Measurements should be made with the unit
ON and OFF, with the power line polarity Normal and Reversed.
Record the highest reading of current.
Figure 10-3. Set Up for Chassis Source Leakage Current, IEC 601-1 Clause 19 -
Continuos Leakage Currents and Patient, Auxiliary Currents
When using the Microguard or a similar test instrument, its power plug may be inserted into the wall outlet and the equipment under test is plugged into the receptacle on the panel of the meter. This places the meter in the grounding conductor and the current flowing from the case to ground will be indicated in any of the current ranges. The maximum allowable limit for chassis source leakage is shown in Table 10-12 on page 10-21.
LOGIQ V2/LOGIQ V1 – Basic Service Manual
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10-25
Care and Maintenance
Data Sheet for enclosure Source Leakage Current
The test passes when all readings measure less than the value shown in Table 10-12 on page 10-21. Record all data on the PM
Inspection Certificate.
Table 10-16: Typical Data Sheet for enclosure Source Leakage Current
Unit
Power
Tester
Polarity
Switch
Tester
Neutral or
Ground
Switch
ON
OFF
OFF
OFF
OFF
Enter Name of tested peripheral here:
ON NORM OPEN
ON
ON
NORM
REV
CLOSED
OPEN
REV
NORM
NORM
REV
REV
CLOSED
OPEN
CLOSED
OPEN
CLOSED
Test 1
Speaker
Cover
Test 2 Real
Panel Metal
Parts
Optional
Test 3
Optional
Test 4
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Electrical safety tests
Probe leakage current test
DANGER
CAUTION
DO NOT USE THE PROBE IF THE INSULATING MATERIAL
HAS BEEN PUNCTURED OR OTHERWISE COMPROMISED.
INTEGRITY OF THE INSULATION MATERIAL AND PATIENT
SAFETY CAN BE VERIFIED BY SAFETY TESTING
ACCORDING TO IEC60601-1.
Equipment damage possibility. Never switch the Polarity and the status of Neutral when the Ultrasound system is powered
ON. Be sure to turn the Ultrasound system power OFF before switching them using the POLARITY switch and/or the
NEUTRAL switch. Otherwise, the Ultrasound system may be damaged.
Definition
This test measures the current that would flow to ground from any of the probes through a patient who is being scanned and becomes grounded by touching some other grounded surface.
NOTE: Some leakage current is expected on each probe, depending on its design. Small variations in probe leakage currents are normal from probe to probe. Other variations will result from differences in line voltage and test lead placement. It is abnormal if no leakage current is measured. If no leakage current is detected, check the configuration of the test equipment.
Tools
For needed tools, see: ‘Tools required’ on page 10-8.
LOGIQ V2/LOGIQ V1 – Basic Service Manual
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10-27
Care and Maintenance
Generic procedure on probe leakage current
H (BLACK)
Measurements should be made with the ground open and closed, with power line polarity normal and reversed, and with the unit Off and On. For each combination, the probe must be active to find the worst case condition.
POLARITY REVERSING SWITCH
PROBE
CONSOLE
N (WHITE)
POWER
OUTLET
G (GREEN)
MOMENTARY
SWITCH
LEAKAGE TEST
METER
Figure 10-4. Set up for probe leakage current
NOTE: Each probe will have some amount of leakage current, dependent on its design. Small variations in probe leakage currents are normal from probe to probe. Other variations will result from differences in line voltage and test lead placement.
DANGER TO AVOID PROBE DAMAGE AND POSSIBLE ELECTRIC
SHOCK, DO NOT IMMERSE PROBES INTO ANY LIQUID
BEYOND THE LEVEL INDICATED IN THE PROBE USERS
MANUAL. DO NOT TOUCH THE PROBE, CONDUCTIVE
LIQUID OR ANY PART OF THE UNIT UNDER TEST WHILE
DOING THE TEST.
Meter Procedure Using Probe Adapter
Follow the Safety Analyzer tool instruction to test each transducer for leakage current.
The electrical Safety Analyzer tool should be calibrated and compliant with AAMI/ESI 1993 or IEC 60601 or AS/NZS 3551.
No Meter Procedure Using Probe Adapter
Follow the Safety Analyzer tool instruction to test each transducer for leakage current.
The electrical Safety Analyzer tool should be calibrated and compliant with AAMI/ESI 1993 or IEC 60601 or AS/NZS 3551.
10-28 LOGIQ V2/LOGIQ V1 – Basic Service Manual
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Electrical safety tests
Data Sheet for Transducer Source Leakage Current
Unit Power
OFF
OFF
OFF
OFF
ON
ON
ON
ON
The test passes when all readings measure less than the values shown in Table 10-13 on page 10-21. Record all data on the PM
Inspection Certificate.
Table 10-17: Typical Data Sheet For Transducer Source Leakage Current
Transducer Tested:
Tester Power Polarity
Switch
Tester GROUND or
NUETRAL Switch
NORM
NORM
REV
REV
NORM
NORM
REV
REV
OPEN
CLOSED
OPEN
CLOSED
OPEN
CLOSED
OPEN
CLOSED
Measurement
LOGIQ V2/LOGIQ V1 – Basic Service Manual
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10-29
Care and Maintenance
When there's too much leakage current …
AC/DC Fails
Where applicable, check the AC/DC adapter and its cable.
Replace a new one if any portion is defective.
Chassis Fails
Check the ground on the power cord and plug for continuity.
Ensure the ground is not broken, frayed, or intermittent. Replace any defective part.
Where applicable, tighten all grounds. Ensure star washers are under all ground studs.
Inspect wiring for bad crimps, poor connections, or damage.
Test the wall outlet; verify it is grounded and is free of other wiring abnormalities. Notify the user or owner to correct any deviations. As a work around, check the other outlets to see if they could be used instead.
NOTE: No outlet tester can detect the condition where the white neutral wire and the green grounding wire are reversed. If later tests indicate high leakage currents, this should be suspected as a possible cause and the outlet wiring should be visually inspected.
10-30 LOGIQ V2/LOGIQ V1 – Basic Service Manual
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When there's too much leakage current …
Probe Fails
Test the probe in another connector to isolate if the fault lies with the probe or the Ultrasound system. Or Change another probe to confirm if the fail is caused by console.
NOTE: Each probe will have some amount of leakage, dependent on its design. Small variations in probe leakage currents are normal from probe to probe. Other variations will result from differences in line voltage and test lead placement. The maximum allowable leakage current for body surface contact probe differs from inter-cavity probe. Be sure to enter the correct probe type in the appropriate space on the check list.
If excessive leakage current is slot dependent, inspect the system connector for bent pins, poor connections, and ground continuity.
If the problem remains with the probe, replace the probe.
Peripheral Fails
Tighten all grounds. Ensure star washers are under all ground studs.
Inspect wiring for bad crimps, poor connections, or damage.
Still Fails
If all else fails, begin isolation by removing the probes, external peripherals, then the on board ones, one at a time while monitoring the leakage current measurement.
New Unit
If the leakage current measurement tests fail on a new
Ultrasound system and if situation can not be corrected, submit a Safety Failure Report to document the Ultrasound system problem. Remove Ultrasound system from operation.
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10-31
Care and Maintenance
Inspection Paperwork
Ultrasound Inspection Forms
ULTRASOUND INSPECTION CERTIFICATE
C u s t o m e r N a m e : S y s t e m I D :
System Type
M o d e l N u m b e r :
P r o b e 1 :
P r o b e 2 :
P r o b e 3 :
P r o b e 4 :
P r o b e 5 :
F r e q u e n c y :
F r e q u e n c y :
F r e q u e n c y :
F r e q u e n c y :
F r e q u e n c y :
S c a n F o r m a t * :
S c a n F o r m a t * :
S c a n F o r m a t * :
S c a n F o r m a t * :
S c a n F o r m a t * :
D i s p a t c h N u m b e r / Date Performed:
S e r i a l N u m b e r :
M o d e l N u m b e r :
M o d e l N u m b e r :
M o d e l N u m b e r :
M o d e l N u m b e r :
M o d e l N u m b e r :
Warranty/C ontract/HBS
M a n u f a c t u r e D a t e :
S e r i a l N u m b e r :
S e r i a l N u m b e r :
S e r i a l N u m b e r :
S e r i a l N u m b e r :
S e r i a l N u m b e r :
* Scan Format: Phased Array, Linear Array, Curved Array, Mechanical Array or Other
Figure 10-5. Ultrasound Inspection Certificate
* Scan Format: Phased Array, Linear Array, Curved Array,
Mechanical Array or Other
10-32 LOGIQ V2/LOGIQ V1 – Basic Service Manual
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Inspection Paperwork
Ultrasound Inspection Forms (continued)
FUNCTIONAL CHECKS
Functional Check (if applicable)
B M o d e F u n c t i o n
D o p p l e r M o d e s F u n c t i o n
C F M o d e F u n c t i o n
M M o d e F u n c t i o n
Applicable Software Opti o n s
A p p il c a b l e H a r d w a r e O p t i o n s
Control Panel
LCD
Measurement Accuracy
GE Approved Peripherals
OK? or
N/A
PHYSICAL IN SPECTION AND CLEANING
Physical Inspection and Cleaning
(if applicable)
C o n s o l e
L C D
E x t e r n a l I / O
C a b l e s a n d C o n n e c t o r s
G E A p p r o v e d P e r i p h e r a l s (DVD-RW, Printer)
L a b e il ng (see User Manual for Labeling)
Inspect Clean
COMMENTS:
_________________________ ____________________________ _________________________
_________________________ ____________________________ _________________________
_________________________ ____________________________ _________________________
_________________________ ____________________________ _________________________
Figure 10-6. Functional Checks
ELECTRICAL SAFETY
Electrical Test Performed
Outlet (correct ground &wiring config.)
Type BF Applied Part Leakage Current
Limits- Probe enclosure Source Leakage Current -
Chassis Leakage Current Limits
Peripheral 1 Leakage Current
Peripheral 2 Leakage Current
Max Value
Allowed
Value
Measured OK?
Comments
PROBES
Probe Number
(from previous page)
Probe 1:
Probe 2:
Max Value
Allowed
Max Value
Measured OK?
Comments
Probe 3:
Final Check. All system covers are in place. System scans with all probes as expected.
Accepted by: ______________________________________________________________________
Figure 10-7. Electrical Safety
LOGIQ V2/LOGIQ V1 – Basic Service Manual
5610739-100 English Rev.3
10-33
Care and Maintenance
Electrical Safety Tests Log
Electrical test performed
Outlet (correct ground and wiring config.)
System ground continuity
Chassis source leakage current - probe
Chassis source leakage current - wheel
Chassis source leakage current - monitor
Patient lead source leakage (lead to ground)
Patient lead source leakage (lead to lead)
Patient lead source leakage (isolation)
Peripheral 1 leakage current
Peripheral 1 ground continuity
Peripheral 2 leakage current
Table 10-18: Electrical safety tests log
Max value allowed
Value measured
OK?
Comments
10-34 LOGIQ V2/LOGIQ V1 – Basic Service Manual
5610739-100 English Rev.3
Electrical Safety Tests Log
Electrical test performed
Table 10-18: Electrical safety tests log (Continued)
Max value allowed
Value measured
OK?
Comments
Peripheral 2 ground continuity
Peripheral 3 leakage current
Peripheral 3 ground continuity
Probe
Table 10-19: Electrical safety tests (probes) log
Max value allowed
Max value measured
OK?
Comments
LOGIQ V2/LOGIQ V1 – Basic Service Manual
5610739-100 English Rev.3
10-35
Care and Maintenance
10-36 LOGIQ V2/LOGIQ V1 – Basic Service Manual
5610739-100 English Rev.3
Index
A
abbrevations, 9-3 acclimate time, 2-3 authorized representative in EU, 1-28 average setup time, 3-3
B
before installation (site preparations), 2-1
Boot Up, 3-17
C
cable inspection mains cable inspection, 10-14 care and maintenance, 10-1 warnings, 10-3
CE compliance, 1-24 change history, i-1 chapter 1 introduction, 1-1 chassis leakage current test, 10-25 cold or hot if the unit is very cold or hot, 2-3 compatibility hardware/software, 9-4 completing the setup, 3-14 compliance, 1-24 configuration, 3-18 connect probe, 3-17 connections on the rear panel, 3-16 console environmental requirements, 2-3 console requirements, 2-3 contact information, 1-26 contents in this manual, 1-3 conventions used in book, 1-6 cooling, 2-5 copyrights, i-14 customer assistance, 1-26 phone numbers, 1-27 customer order verification, 3-13 customer provided prerequisite, 8-8
LOGIQ V2/LOGIQ V1 – Basic Service Manual
5610739-100 English Rev.3
D
damage in transportation, 3-7 damage in transport, i-11 dangerous procedure warnings, 1-21 data network setup requirements, 2-19 desirable features, 2-15
DICOM network function, 2-19
DICOM setup requirements, 2-20 display PDF files from manual CD-ROM print PDF files from manual CD-ROM, 4-21
E
electrical requirements, 2-6
EMI limitations
EMI limitations, 2-9 general requirements, 2-6 site circuit breaker site circuit breaker, 2-7 site power outlets site power outlets, 2-7 specific requirements for the unit, 2-6 unit power plug unit power plug, 2-7 electrical safety, 1-17 electrical safety tests, 10-19 electrical specification, 3-15 electromagnetic interference abatement, 2-10 prevention, 2-10 electrostatic discharge prevention, 1-25
EMC, 1-24 compliance, 1-24 what is EMC?, 1-24
EMI, 1-24 abatement, 2-10 prevention, 2-10 protection, 3-13 environmental dangers, 2-22 environmental specifications for the unit, 2-4 errors, i-12
ESD, 1-24
ESD prevention, 1-25 examine packages, 3-6
Index-1
external I/O connections, 3-16
F
facility needs, 2-12 desirable features, 2-15
DICOM network function, 2-19
DICOM setup requirements, 2-20
InSite requirements, 2-19 network setup requirements, 2-19 purchaser responsibilities, 2-13 recommended floor plan suggestion, 2-17 required facility needs, 2-14 suggested floor plan scanner and EchoPAC in same room, 2-18 floor plan suggestion recommended, 2-17 scanner and EchoPAC in same room, 2-18 functional checks, 10-13 mains cable inspection, 10-14 system checks, 10-13
G
GE Healthcare leakage current limits, 10-21 general console requirements, 2-3 generic procedure on probe leakage current, 10-28 grounding continuity, 10-24
H
I
hardware/software compatibility, 9-4 hardware-software compatibility, 5-3 hot or cold if the unit is very cold or hot, 2-3 how often should maintenance tasks be performed?,
10-6
human safety, 1-12 icons, 1-6 icons indicating a special procedure to be used, 1-9 if the unit is very cold or hot, 2-3 important precautions, i-2
InSite network requirements, 2-19 installation see "system setup", 3-1 installation warnings see "setup warnings", 3-3 introduction (chapter 1), 1-1
L
legal notes, i-14 lighting, 2-5 list of abbrevations, 9-3 loading software, 8-8 lockout/tagout (LOTO) requirements, 1-22
LOTO lockout/tagout requirements, 1-22
M
mains cable inspection, 10-14 maintenance physical inspection, 10-15 preliminary checks, 10-12 system maintenance, 10-12 maintenance task schedule, 10-6 manufacturer, 1-27 mass with monitor and peripherals, 3-14 mechanical safety, 1-15 model designations, 1-6 models covered by this manual, 1-5
N
network setup requirements, 2-19
O
omission and errors, i-12 operational and storage temperature for probes, 2-11
P
packing materials recycling information, 3-12 paperwork after setup, 3-41
PDF files display and print, 4-21 periodic maintenance inspection (PM), PM (periodic maintenance inspection), 10-4 phone numbers customer assistance, 1-27 physical dimensions, 3-14 physical inspection at arrivel, 3-13
Power On, 3-17 precautions certified electrical contractor statement, i-11 damage in transport, i-11 important precautions, i-2 service safety considerations, i-13 translation policy, i-2 prepeare for setup, 3-13 prerequisite provided by customer, 8-8 probe connect, 3-17 probe cleaning, 10-18 probe leakage current test, 10-27
Index-2 LOGIQ V2/LOGIQ V1 – Basic Service Manual
5610739-100 English Rev.3
probe maintenance, 10-17 basic probe care, 10-17 basic probe cleaning, 10-18 probe related checks, 10-17 probe related checks, 10-17 probes environmental requirements, 2-11 operational and storage temperature for probes,
2-11
product icons, 1-10 product locator installation card, 3-41 products covered by this manual, 1-5
Purchaser responsibilities, 2-13
R
rear panel connections, 3-16 receiving and unpacking, 3-6 receiving the product, 3-6 recycling information packing materials, 3-12 required facility needs, 2-14 requirements, 2-3 requirements verification, 3-14 returning/shipping probes and repair parts, 1-23 revision history, i-1
S
safety human, 1-12 safety precaution messages, 1-7 safety test overview, 10-19 service safety considerations, i-13 setup completion, 3-14 preparations, 3-13 reminders, 3-3 setup time, 3-3 setup warnings, 3-3 shipping/returning probes and repair parts, 1-23 site preparations, 2-1 time and manpower requirements, 2-11 software loading, 8-8 software/hardware compatibility, 9-4 software-hardware compatibility, 5-3 specifications, 3-14 electrical specifications, 3-15 physical dimensions, 3-14 standard GE tool kit, 10-8 standard hazard icons, 1-8 statement certified electrical contractor statement, i-11 system specifications, 3-14 system checks, 10-13 system maintenance, 10-12 physical inspection, 10-15 preliminary checks, 10-12 system manufacturer, 1-27 system requirements verification, 3-14 system setup, 3-1
T
time and manpower requirements site preparations, 2-11 tools required, 10-8 special tools, supplies and equipment, 10-11 standard GE tool kit, 10-8 trademarks, i-14 translation policy, i-2 transport damage, i-11 typical users of the service manual, 1-4
U
unpacking, 3-6 unpacking instructions, 3-8
V
verification system requirements, 3-14 verify customer order, 3-13 voltage settings, 3-15
W
warnings, 10-3 dangerous procedures, 1-21 receiving and unpacking, 3-6 what is EMC?, 1-24 when there’s too much leakage current, 10-30 chassis fails, 10-30 new unit, 10-31 peripheral fails, 10-31 probe fails, 10-31 still fails, 10-31
LOGIQ V2/LOGIQ V1 – Basic Service Manual
5610739-100 English Rev.3
Index-3
Index-4 LOGIQ V2/LOGIQ V1 – Basic Service Manual
5610739-100 English Rev.3
GE
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