Ultrasound Systems Common Service Information Rev 6

Manufacturer: GE Medical Systems www.gehealthcare.com

Revision History Reason for Change DATE (YYYY/MM/DD)

REVISION

REASON FOR CHANGE

1

2012/01/30

Initial Release

2

2013/12/16

Updated according to feedback.

3

2014/11/04

Adding New Products

4

2016/01/29

Updated according to feedback.

5

2018/08/21

Updated according to feedback.

6

2022/05/05

Updated according to feedback.

List of Effective Pages (LOEP)

PAGE NUMBER

REVISION NUMBER

PAGE NUMBER

REVISION NUMBER

Title Page

Rev. 6

Table of Contents

Rev. 6

Revision History

Rev. 6

Chapters 1 through 4

Rev. 6

Important precautions

Rev. 6

Index

Rev. 6

Please verify that you are using the latest revision of this document. Information pertaining to this document is maintained on MyWorkshop. 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. Note: Testing requirements and descriptions of the safety equipment in this Common Service Information (CSI) Manual supersedes the product’s Service Manual if that manual’s publication date precedes the date of this CSI manual.

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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 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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Ultrasound System – Common Service Information 5444964-100 English Rev. 6

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

GE Service Documentation 9900 Innovation Drive (RP-2156) WAUWATOSA, WI 53226 USA GE employees should use Post-Market Quality Management (PQM) to report service documentation issues.

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 pads, to reduce the risk of injury. For a complete review of all safety requirements, see: ‘Safety Information’ on page 2-1.

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Legal notes The contents of this publication may not be copied or duplicated in any form, in whole or in part, without prior written permission of GE. GE makes no representations or warranties with respect to the information herein. In addition, the information is subject to change without notice. Every precaution has been taken in the preparation of this document. Nevertheless, GE assumes no responsibility for errors, omissions, or any damages, including special or consequential, resulting from the use of this information. GE will issue updates to this information periodically, as needed. If there are any questions regarding the information contained in this manual, please contact your GE Representative.

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

Copyrights © GE, 2013-2022. All Rights Reserved.

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Ultrasound System – Common Service Information 5444964-100 English Rev. 6

Table of Contents

Translation policy - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-2 Damage in transportation - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-6 Certified electrical contractor statement - For USA only - - - - - - - - - - - - - i-6 Omission and errors - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-7 Service safety considerations- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-7 Legal notes - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-8 Trademarks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-8 Copyrights - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-8

Chapter 1 - Overview Contents of this Manual Product Description Overview of the Ultrasound system - - - - - - - - - - - - - - - - - - - - - - - - - - 1-3

Products Covered in this Manual

Chapter 2 - Safety Information Overview Contents in this chapter- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-2

Important Conventions Conventions used in book - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-3 Standard hazard icons - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-5

Product Icons Label icon description - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-7 How to lock the operator panel prior to transport - - - - - - - - - - - - - - - - - 2-7

Safety Considerations Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-8 Human safety - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-8 Mechanical safety - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-11 Electrical safety - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-16

Label Locations Product labels - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-18

Dangerous Procedure Warnings Warnings - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-19

Lockout/Tagout (LOTO) LOTO requirements - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-20

Returning Probes and Repair Parts Requirements for returning parts - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-21 User responsibility - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-22

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Electromagnetic Compatibility (EMC) What is EMC? - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-23 Compliance - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-23 Electrostatic discharge (ESD) prevention - - - - - - - - - - - - - - - - - - - - - 2-24

Chapter 3 - Site Preparations Overview Contents in this chapter- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-2

General Ultrasound System Requirements Contents in this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-3 Ultrasound system environmental requirements- - - - - - - - - - - - - - - - - - 3-3 Electrical requirements - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-5 EMI limitations - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-18 Probes environmental requirements - - - - - - - - - - - - - - - - - - - - - - - - - 3-20 Time and manpower requirements - - - - - - - - - - - - - - - - - - - - - - - - - - 3-20

Facility Needs Contents in this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-21 Purchaser responsibilities - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-21 Required facility needs - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-23 Desirable features- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-25

Chapter 4 - Care and Maintenance Overview Care and maintenance - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-2 Contents in this chapter- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-2

Warnings Warnings - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-3

Why Do Maintenance Keeping records - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-4 Quality assurance - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-4

Maintenance Task Schedule How often should maintenance tasks be performed? - - - - - - - - - - - - - - 4-5

System Maintenance Preliminary checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-6 Functional checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-7 Physical inspection - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-9 Cleaning - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-11 Probe maintenance- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-12

Using a Phantom Phantoms - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-13

Electrical Safety Tests Content in this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-14 Uninterrupted power supply (UPS) - - - - - - - - - - - - - - - - - - - - - - - - - - 4-15 Safety test overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-16 Leakage current limits - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-18 Outlet test - wiring arrangement - USA and Canada - - - - - - - - - - - - - - 4-21 Grounding continuity - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-22 Chassis leakage current test - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-23 Isolated patient lead (source) leakage–lead to ground - - - - - - - - - - - - 4-26

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Isolated patient lead (source) leakage–lead to lead - - - - - - - - - - - - - - 4-29 Isolated patient lead (sink) leakage-isolation test - - - - - - - - - - - - - - - - 4-31 Probe (source) leakage current test - - - - - - - - - - - - - - - - - - - - - - - - - 4-33 Isolated probe (sink) leakage-isolation test - - - - - - - - - - - - - - - - - - - - 4-38

When There Is Too Much Leakage Current AC/DC fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-42 Chassis fails- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-42 Probe fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-43 Peripheral fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-43 Still fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-43 New Ultrasound system- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-43 ECG fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-43

Ultrasound Equipment Quality Check (EQC and IQC) Quality checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-44

Index

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Chapter 1 Overview This Service Manual includes common service information for GE Ultrasound systems. The manual provides Installation, Safety, and Maintenance information.

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Overview

Contents of this Manual

The following topics are covered in this manual:

1-2

•

Products covered in this manual. See Chapter 1 (this chapter).

•

Safety Information. See Chapter 2.

•

Site Preparations. See Chapter 3.

•

Care and Maintenance. See Chapter 4.

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Product Description

Product Description

Overview of the Ultrasound system This Ultrasound System is a high performance digital ultrasound imaging system with total data management. The fully digital architecture of the Ultrasound system allows optimal usage of all scanning modes and probe types throughout the full spectrum of operating frequencies. Signal flows from the Probe Connector Panel through the Ultrasound system and finally to the monitor and peripherals. System configuration is stored on the hard drive. All necessary software is loaded from the hard drive on power up.

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Overview

Products Covered in this Manual

This Common Service Information (CSI) Manual is effective for the products listed in Table 1-1. NOTE:

Ultrasound products that are software only or are not connected to power when scanning are not included in Table 1-1. Testing requirements and descriptions of the safety equipment in this Common Service Information (CSI) Manual supersedes the product’s Service Manual if that manual’s publication date is earlier than the date of this CSI manual.

Table 1-1:

Ultrasound Products Covered in this Manual

Invenia ABUS

Vivid in

Voluson e

LOGIQ S8

LOGIQ V3

Vivid 7/E9/E7

Vivid e*

Voluson Expert 22

LOGIQ P7/P8/P9

LOGIQ i*

Vivid E80/E90/E95

Vivid iq*

Voluson SWIFT

LOGIQ P10

LOGIQ e*

Vivid S60/S70

Vivid q

Versana Active

LOGIQ S7

LOGIQ Book*

Vivid S60N/S70N

Vivid q N

Versana Balance

LOGIQ 7

LOGIQ Book XP*

Vivid T9

Voluson 730

Versana Essential

LOGIQ S6

LOGIQ C2/3/5

Vivid T8/T8 Pro

Voluson E10

Versana Premier

LOGIQ 5

LOGIQ e Vet*

Vivid S6/S6 N

Voluson E8

LOGIQ E10

LOGIQ P6

LOGIQ F Series

Vivid S5/S5 N

Voluson E6

LOGIQ E11/E20

LOGIQ P5/A5

LOGIQ C9 Series

Vivid 3

Voluson S6/S8

LOGIQ E10s

LOGIQ 3

LOGIQworks Workstation

Vivid 3n

Voluson S10

LOGIQ Fortis

LOGIQ P3

LOGIQ V2/V1

Vivid 4

Voluson P6

LOGIQ E9

LOGIQ C3

Venue*

Vivid P3

Voluson P8

LOGIQ 9

LOGIQ C5

Venue 40/50

Vivid i*

Voluson i

LOGIQ E8

LOGIQ V5

Venue Go Venue Fit

* These products may include docking and isolation carts (with different electrical specifications).

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Chapter 2 Safety Information 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 Ultrasound system.

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2-1

Safety Information

Overview

Contents in this chapter

2-2

•

‘Important Conventions’ on page 2-3

•

‘Product Icons’ on page 2-7

•

‘Safety Considerations’ on page 2-8

•

‘Label Locations’ on page 2-18

•

‘Dangerous Procedure Warnings’ on page 2-19

•

‘Lockout/Tagout (LOTO)’ on page 2-20

•

‘Returning Probes and Repair Parts’ on page 2-21

•

‘Electromagnetic Compatibility (EMC)’ on page 2-23

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