General Electric Vivid S60 - Vivid S70 Basic Service Manual - v203_SM_BC291740-1EN_1 IMAGEWELL IMAGE CAPTURE KIT WITH SOFTWARE Owners Manual

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PRELIMINARY

29.JAN.2019 VS60-VS70_FRNT_CVR.FM

Technical Publication

VIVID™ S60 AND VIVID™ S70

Vivid™ S60/S70 Basic Service Manual

Software version v203

Direction Number: BC291740-1EN Revision: Rev. 1

BASIC SERVICE DOCUMENTATION. COPYRIGHT GENERAL ELECTRIC COMPANY.

PRELIMINARY

29.JAN.2019 VS60-VS70_FRNT_CVR.FM

Manufacturer:

GE Medical Systems, Israel Ltd. Nativ Ha'or Street no. 1 3508510 Haifa ISRAEL Tel: (+972) 4851 9555 Fax: (+972) 4851 9500

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Important Precautions

TRANSLATION POLICY

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DANGER

WARNINGWARNING

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

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. Othe r conn ections between pieces o f electrical equipment, calibrations and testing sh all be per fo rme d by qu a lifie d G E pe rso n nel. 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 e lectricians) to perform electrical servicing on the equipment.

OMISSIONS & ERRORS

If there are any omissions, errors or suggestions for improving this documentation, please contact the GE 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: Service Documentation, GE Vingmed Ultrasound AS

P.O.Box: 141 3191 HORTEN NORWAY

GE employees should use Post-Market Quality Management (PQM) to report service documentation issues.

SERVICE SAFETY CONSIDERATIONS

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

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

For a complete review of all safety requirements, see the Chapter 1 Safety Considerations section in the Service Manual.

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LEGAL NOTES

The contents of this publication may not be copied or duplicated in any form, in whole or in part, without prior written permission of GE.

GE 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 th ere are an y questions rega rding the in formation contain ed in this manual, please contact your GE Representative.'

TRADEMARKS

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

COPYRIGHTS

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IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Revision History

Revision

Date

(DD.MM.YYYY)

25.02.2019

Reason for change

Initial release of Basic Service Manual for systems updated to v203.

List of Effected Pages (LOEP)

Pages Revision Pages Revision Pages Revision

Title Page 1 4-1 to 4-46 1 10-1 to 10-36 1

Important Precautions

-i to -xvi TOC 1 6-1 to 6-4 1

1-1 to 1-32 1 7-1 to 7-30 1 2-1 to 2-16 1 8-1 to 8-154 1 3-1 to 3-76 1 9-1 to 9-32 1

1 5-1 to 5-32 1 Back Cover N/A

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IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

CHAPTER 1 Introduction

Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 1

Purpose of Chapter 1 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 1

Contents in this Chapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 1

Service Manual Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 2

Contents in this Service Manual . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 2

Typical Users of the Basic Service Manual . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 3

Vivid™ S60/Vivid™ S70 Models Covered in this Manual . . . . . . . . . . . . . . . . . 1 - 4

Product Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 5

Important Conventions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 6

Conventions Used in this Manual . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 6

Standard Hazard Icons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 7

Safety Considerations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 8

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 8

Human Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 8

Mechanical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 10

Electrical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 12

Vivid™ S60/Vivid™ S70 Battery Safety (part of Power Supply) . . . . . . . . . . . . 1 - 14

Patient Data Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 14

Dangerous Procedure Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 15

Lockout/Tagout (LOTO) Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 16

Product Labels and Icons. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 17

Universal Product Labels . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 17

Label Descriptions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 21

Vivid™ S60/Vivid™ S70 External Labels . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 25

Returning/Shipping Probes and Repair Parts. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 26

EMC, EMI, and ESD. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 27

Electromagnetic Compatibility (EMC) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 27

CE Compliance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 27

Electrostatic Discharge (ESD) Prevention . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 28

General Caution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 28

Customer Assistance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 29

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Contact Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 29

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IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

CHAPTER 2 Site Preparations

Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 1

Purpose of Chapter 2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 1

Console Requirements. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 2

Unit Environmental Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2

Cooling Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2

Lighting Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2

Time and Manpower Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 2

Electrical Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 3

EMI Limitations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 4

EMI Prevention/Abatement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 5

Probe Environmental Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 5

Facility Needs. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 6

Purchaser Responsibilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 6

Mandatory Site Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 7

Site Recommendations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 7

Networking Pre-Installation Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 - 12

Connectivity Installation Worksheet . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2 - 13

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CHAPTER 3 System Setup

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 1

Purpose of Chapter 3 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 1

Setup Reminders. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 2

Average Setup Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 2

Setup Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 2

Safety Reminders . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 4

Receiving and Unpacking the Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 5

Warnings for Receiving and Unpacking the Equipment . . . . . . . . . . . . . . . . . . . 3 - 5

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 5

Additional labels on the Shipping Carton . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 9

Unpacking the Vivid™ S60/Vivid™ S70 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 10

Physical Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 20

EMI Protection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 20

Preparing for Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 21

Verifying Customer Order . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 21

Physical Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 21

Component Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 21

EMI Protection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 25

Completing the Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 26

Purpose of this Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 26

System Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 26

Electrical Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 28

Connections on the I/O Rear Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 28

Connections on the Patient I/O Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 29

Connecting Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 30

Power on/Boot up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 32

Power Shut Down . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 32

Complete Power Down . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 32

Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 33

Purpose of this Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 33

Ultrasound System Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 33

Service Screen Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 39

Optional Peripherals/Peripheral Connection . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 42

Software Options Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 44

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IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Connectivity Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 45

Physical Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 45

Stand-alone ultrasound system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 45

“Sneaker Net” Environment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 45

Wired Ethernet from ultrasound system to a Workstation . . . . . . . . . . . . . . . . 3 - 45

Connection from ultrasound system to a DICOM Server on a Network . . . . . . 3 - 45

Connectivity Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 46

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 46

Compatibility . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 46

Select TCP/IP Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 47

Changing the AE Title and/or Port Number (Port No.) . . . . . . . . . . . . . . . . . . . 3 - 48

Set the Remote Archive’s Network Information . . . . . . . . . . . . . . . . . . . . . . . . 3 - 48

Save the New Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 49

Wireless Network Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 50

Options Setup. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 51

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 51

Software Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 51

Color Video Printer Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 51

USB Flash Card Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 51

Tricefy™ . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 52

Wireless Network Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 53

Installation and set up of the View-X function . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 68

CARTO interface installation overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 69

Verifying/Installing SW option keys . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 72

External Monitor Output Resolution Adjustment . . . . . . . . . . . . . . . . . . . . . . . . 3 - 74

Paperwork After Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 75

Installation Acceptance Test Criteria . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 75

User’s Manual(s) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 75

Product Locator Installation Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 75

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CHAPTER 4 General Procedures and Functional Checks

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 1

Purpose of Chapter 4 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 1

Special Equipment Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 1

General Procedures. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 2

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 2

Power On-Off . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 3

Logging On to the Vivid™ S60/Vivid™ S70 as “ADM” . . . . . . . . . . . . . . . . . . . . 4 - 9

Install the On-board User Manuals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 10

Changing Passwords . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 11

Security setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 12

Data Management . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 13

Deleting Patient Information (PHI) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 14

LCD Monitor Position Adjustment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 15

Moving and Transporting the Vivid S60/Vivid S70 Ultrasound Scanner . . . . . 4 - 16

Cleaning the Trackball . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 19

Functional Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 20

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 20

Performance Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 20

2D Mode (B Mode) Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 21

M Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 24

Color Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 27

PW/CW Doppler Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 32

Tissue Velocity Imaging (TVI) Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 35

Probe/Connectors Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 38

ECG Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 39

Cineloop Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 40

Back End Processor Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 41

Operating Panel Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 41

Main OLED/LCD Screen Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 42

External Monitor Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 42

Peripheral Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 42

Mechanical Functions Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 44

-vi Table of Contents

PRELIMINARY

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

CHAPTER 5 Components and Function (Theory)

Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 1

Purpose of Chapter 5 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 1

General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 2

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 2

Vivid™ S60/Vivid™ S70 System Design . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 4

User Interface Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 5

Main Scanner Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 5

Power Supply Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 5

Vivid™ S60/Vivid™ S70 Ultrasound Scanner - Positioning Capabilities . . . . . . . . . . . . .5 - 6

System Up and Down Positions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 6

Upper Section - Positioning Control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 7

Main Display - Articulated Arm . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 8

Main Display - Positioning Capabilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 9

System Positioning for Transportation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 10

Vivid™ S60/Vivid™ S70 Ultrasound Scanner - Electronic Cage (v203) . . . . . . . . . . . 5 - 11

Scanner Electronic Cage - Main Assemblies (v203) . . . . . . . . . . . . . . . . . . . . 5 - 11

Service Access to the Vivid™ S60/Vivid™ S70 System Modules . . . . . . . . . . . . . . . . .5 - 14

Modules Accessed from the Front (v203) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 14

Modules Accessed from the Rear . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 15

Top Console with Monitor, Operator Control Panel and Touch Screen . . . . . . . . . . . . .5 - 16

Monitor (Main Display) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 16

Operator Control Panel and Speakers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 16

Touch Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 19

Internal and External Input/Output . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 20

Front End Unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 21

General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 21

Components in the Electronic Cage Assembly . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 22

Front End Power Supply (FEPS) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 23

Front End (cFE) Board . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 23

Probe Selection Board (PSB) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 24

Patient I/O Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 24

Table of Contents -vii

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Back End Unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 25

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 25

System Power Distribution. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 26

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 26

System Power Management . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 27

Rechargeable Battery Pack . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 27

Cooling System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 29

General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 29

Peripherals. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 30

Internal Peripheral . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 30

External Peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 30

Service Desktop - v203 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 31

-viii Table of Contents

PRELIMINARY

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

CHAPTER 6 Service Adjustments

Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6 - 1

Purpose of Chapter 6 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 1

Contents in this Chapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 1

Power Supply Adjustments. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 2

Monitor Adjustments. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6 - 2

Using monitor adjustment touch panel controls . . . . . . . . . . . . . . . . . . . . . . . . . 6 - 2

Touch Panel adjustments. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6 - 3

Table of Contents -ix

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

CHAPTER 7 Diagnostics/ Troubleshooting

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 1

Purpose of Chapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 1

Service Safety Considerations. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 2

Gathering Troubleshooting Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 3

Purpose of this Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 3

Collect Vital System Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 3

Collecting a screen capture with logs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 4

Screen Captures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 5

Purpose of this Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 5

Ctrl+PrintScreen Shortcut . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 5

Collecting a screen capture with logs (v203) . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 5

Capturing network logs to use for troubleshooting (v203) . . . . . . . . . . . . . . . . . 7 - 7

Service desktop . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 9

Purpose of this section (v203) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 9

Disruptive mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 10

Color statuses . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 10

Licenses . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 11

Home . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 12

Utilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 16

Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 26

Noise Troubleshooting. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 27

Purpose of this Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 27

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 27

Overview of Types of Noise . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 27

Different Power Outlet . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 29

Different System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 29

Different Location . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 29

Disconnect External Cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 29

-x Table of Contents

PRELIMINARY

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

CHAPTER 8 Replacement Procedures

Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 1

Purpose of Chapter 8 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 1

Covers - Replacement Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8 - 2

Overview of Covers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 2

Air Inlet (Left Side) Cover Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . 8 - 5

Right Side Cover Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 8

DVD Cover Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 9

DVD and Printer Cover Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . 8 - 11

Blank Cover Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 13

Printer Cover Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 15

Front Cover Replacement Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 17

Right Rear Cover Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 22

Left Rear Cover Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 25

OPIO Basket Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 29

Rear Folder Box Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 30

AC Distribution Box Cover Replacement Procedure . . . . . . . . . . . . . . . . . . . . 8 - 32

Control Console Components - Replacement Procedures. . . . . . . . . . . . . . . . . . . . . . .8 - 34

21.5" Monitor Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 34

Touch Screen Service Cover Replacement Procedure . . . . . . . . . . . . . . . . . . 8 - 37

Touch Screen Rear Cover Replacement Procedure . . . . . . . . . . . . . . . . . . . . 8 - 38

Touch Screen Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 41

Touch Screen Rotaries Board Replacement Procedure . . . . . . . . . . . . . . . . . . 8 - 46

Operating Panel Keyboard Assembly Replacement Procedure . . . . . . . . . . . . 8 - 49

Operating Panel GE Logo 40 mm Replacement Procedure . . . . . . . . . . . . . . . 8 - 53

Operating Panel Label Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . 8 - 54

Probe Cup Holders Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 55

Alphanumeric Keyboard Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . 8 - 56

Mechanical Trackball and Housing Replacement Procedure . . . . . . . . . . . . . . 8 - 60

Rotary Knob Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 63

Operating Panel Keycaps Replacement Procedure . . . . . . . . . . . . . . . . . . . . . 8 - 64

Alphanumeric Keycaps Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . 8 - 65

Cables (v203) - Replacement Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 66

Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 66

Time Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 66

Removal Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 66

Mounting Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 68

Table of Contents -xi

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Electronic Cage Components Replacement Procedures for mini-cSound (v203) . . . . 8 - 69

Scanner Electronic Cage (Ecage) Replacement (v203) . . . . . . . . . . . . . . . . . 8 - 70

BEP&CPU Module Replacement (v203) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 73

GPU Module Replacement (v203) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 76

CMST Module Replacement (v203) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 78

CWD Replacement (v203) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 81

ECG Module Replacement (v203) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 83

PSB Module Replacement (v203) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 86

Hard Disk Module Replacement (v203) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 87

FEPS Module Replacement (v203) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 89

Fan Module Replacement (v203) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 92

BIF Module Replacement (v203) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 94

AC Distribution Box Replacement Procedure (v203) . . . . . . . . . . . . . . . . . . . . 8 - 97

Mechanical Platform Components - Replacement Procedures . . . . . . . . . . . . . . . . . . 8 - 101

Mechanical Assembly Base Console Replacement . . . . . . . . . . . . . . . . . . . . 8 - 101

Column Main Support Assembly Replacement . . . . . . . . . . . . . . . . . . . . . . . 8 - 101

Mechanical Assembly Interface Base for the Operating Panel Replacement 8 - 101

Touch Screen Chassis Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . 8 - 101

LCD Arm Alton 21.5in Wide Replacement Procedure . . . . . . . . . . . . . . . . . . 8 - 104

LCD Arm Riser for 21.5 inch monitor replacement procedure . . . . . . . . . . . . 8 - 107

Swivel and Up-Down Handle Replacement Procedure . . . . . . . . . . . . . . . . . 8 - 109

Rear Handle Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 112

Lower Arm Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 114

Gas Spring Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 119

Articulated Arm Release Module Replacement Procedure . . . . . . . . . . . . . . 8 - 123

First Axis with Pin Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 126

Peripherals Console Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . 8 - 129

Probe Shelf Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 131

Probe Cable Holder Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . 8 - 132

Brake and Locking Wheels Replacement Procedure . . . . . . . . . . . . . . . . . . . 8 - 136

Operating System and/or Application Software Loading Procedures . . . . . . . . . . . . 8 - 138

Software Installation Procedures - General Overview . . . . . . . . . . . . . . . . . . 8 - 138

Preparation for Software Installation Procedures . . . . . . . . . . . . . . . . . . . . . . 8 - 139

System Software and/or Application Software Installation (v203) . . . . . . . . . 8 - 140

Peripherals - Replacement Procedures. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 150

DVD/CD-RW Drive Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 150

Black and White Printer Replacement Procedure . . . . . . . . . . . . . . . . . . . . . 8 - 152

-xii Table of Contents

PRELIMINARY

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

CHAPTER 9 Renewal Parts

Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 1

Purpose of Chapter 9 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 1

List of Abbreviations. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 2

Renewal Parts Lists and Diagrams . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 3

Mechanical Hardware Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 3

Covers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 7

Monitor Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 12

Operating Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 13

Power Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 18

Back End Unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 19

Front End Unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 20

FEPS and Ecage (v203) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 22

Electro Mechanical Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 23

Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 24

Cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 25

Optional Peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 30

Jigs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 32

Table of Contents -xiii

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

CHAPTER 10 Care and Maintenance

Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10 - 1

Purpose of Chapter 10 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 1

Care and Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 1

Contents in this chapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 1

Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 2

Why do Maintenance. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 3

Keeping Records . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 3

Quality Assurance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 3

Maintenance Task Schedule . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 4

How often should maintenance tasks be performed? . . . . . . . . . . . . . . . . . . . 10 - 4

System Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 6

Preliminary Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 6

Functional Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 7

Physical Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 9

Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 10

Probe Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 11

Probe Related Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 11

Probe Handling . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 12

Basic Probe Care . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 12

Returning and Shipping of Defective Probes . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 13

Phantoms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 13

Electrical Safety Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 14

Safety Test Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 14

Leakage Current Limits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 16

Outlet Test - Wiring Arrangement - USA and Canada . . . . . . . . . . . . . . . . . . 10 - 19

Grounding Continuity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 20

Chassis Leakage Current Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 21

Isolated Patient Lead (Source) Leakage – Lead-to-Ground . . . . . . . . . . . . . 10 - 24

Isolated Patient Lead (Source) Leakage – Lead-to-Lead . . . . . . . . . . . . . . . 10 - 26

Isolated Patient Lead (Sink) Leakage - Isolation Test . . . . . . . . . . . . . . . . . . 10 - 28

Probe (Source) Leakage Current Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 - 29

Isolated Probe (Sink) Leakage-Isolation Test . . . . . . . . . . . . . . . . . . . . . . . . 10 - 32

-xiv Table of Contents

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Chapter 1

Introduction

Section 1-1 Overview

1-1-1 Purpose of Chapter 1

This chapter describes important issues related to safely servicing the Vivid™ S60/Vivid™ S70 ultrasound scanner. The service provider mu st read and under stand all the information presented here before installing or servicing a unit.

1-1-2 Contents in this Chapter

1-1 Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-1

1-2 Service Manual Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2

1-3 Important Conventions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-6

1-4 Safety Considerations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-8

1-5 Dangerous Procedure Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-15

1-6 Lockout/Tagout (LOTO) Requirements. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-16

1-7 Product Labels and Icons. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-17

1-8 Returning/Shipping Probes and Repair Parts. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-26

1-9 EMC, EMI, and ESD. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-27

1-10 Customer Assistance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-29

Chapter 1 - Introduction 1-1

PRELIMINARY

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Section 1-2 Service Manual Overview

This manual provides setup and service information for the Vivid™ S60/Vivid™ S70 ultrasound

scanner. The ten chapters it contains are outlined in Table 1-1 be lo w.

1-2-1 Contents in this Service Manual

The service manual is divided into ten chapters.

In the beginning of the manual, before chapter 1, you will find the language policy for GE service

documentation, legal information, a revision overview and the Table of Contents (TOC).

Table 1-1 Contents in this Service Manual

CHP NUMBER TITLE DESCRIPTION

Chapter 1 Introduction

Chapter 2 Site Preparations

Chapter 3 System Setup

Chapter 4

Chapter 5

Chapter 6 Service Adjustments

Chapter 7 Diagnostics/ Troubleshooting

Chapter 8 Replacement Procedures

Chapter 9 Renewal Parts

Chapter 10 Care and Maintenance

General Procedures and Functional Checks

Components and Function (Theory)

Contains a content summary and warnings. Contains pre-setup requirements for the Vivid™ S60/Vivid™ S70

ultrasound scanner. Contains setup procedure with an setup checklist.

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

Contains block diagrams and functional explanations of the electronic circuits.

Contains instructions on how to make any available service adjustments to t he Vivid™ S60/Vivid™ S70 ultrasound scanner.

Provides instructions for setting up and running diagnostic, troubleshooting and other related routines for the Vivid™ S60/ Vivid™ S70 ultrasound scanner.

Provides removal and installation procedures for replacement of all Field Replaceable Units (FRUs).

Contains a complete list of field replaceable parts for the Vivid™ S60/Vivid™ S70 ultrasound scanner.

Provides periodic maintenance procedures for the Vivid™ S60/ Vivid™ S70 ultrasound scanner.

NOTE: The illustrations provided in this service manual are for illustration purposes only and are subject to

change without notice.

1-2 Section 1-1 - Overview

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

1-2-2 Typical Users of the Basic Service Manual

This manual is intended for the following categories of users:

• Service personnel (setup, maintenance, etc.).

• Hospital’s service personnel

• Architectural planners/installation planners (some parts of Chapter 2 - Site Preparations).

Chapter 1 - Introduction 1-3

PRELIMINARY

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

1-2-3 Vivid™ S60/Vivid™ S70 Models Covered in this Manual

Table 1-2 Vivid™ S60/Vivid™ S70 Models - updated to v203

Traced

PSI Group Cat No. Description PSI

Vivid™ S70 H45041SW Vivid™ S70 ultrasound imaging scanner Vivid™ S60 H45041SU Vivid™ S60 ultrasound imaging scanner

Code

UVS70A 23908A ES70 UVS60A 23909A ES60

Code

Kisyu

Code

Siebel

Yes Yes

1-4 Section 1-1 - Overview

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

1-2-4 Product Description

1-2-4-1 Overview of the Vivid™ S60/Vivid™ S70 Ultrasound Scanner

The Vivid™ S60/Vivid™ S70 is a compact, phased, linear array ultrasound imaging scanner. Weighing only 75 kg (165 lb), each system is extremely versatile and, depending upon the installed software, can be used for a variety of applications.

The system provides image generation in 2D, Color Dopp ler, Power Dopp ler, M-Mode, Color M-Mode, PW and 4D, Tissue Velocity imaging, and Contrast applications.

The fully digital architecture of the Vivid™ S60/Vivid™ S70 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 to the Front End, and then over to the Back End Processor and finally to the monitor and peripherals.

System configuration is stored on the Vivid™ S60/Vivid™ S70. All necessary software is loaded from the hard drive on power up.

1-2-4-2 Purpose of Operator Manual(s)

The Operator Manual(s) should be fully read and understood before operating the Vivid™ S60/Vivid™ S70 system, and also kept near the unit for quick reference.

Chapter 1 - Introduction 1-5

PRELIMINARY

DANGER

WARNINGWARNING

CAUTION

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Section 1-3 Important Conventions

1-3-1 Conventions Used in this Manual

1-3-1-1 Model Designations

This manual covers the Vivid™ S60/Vivid™ S70 ultrasound units listed in Vivid™ S60/Vivid™ S70

Models Covered in this Manual on page 1-4.

1-3-1-2 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.

1-3-1-3 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 identifi ed by a flag word that precedes the precautionary

message. Known or potential hazards to personal are labeled in one of three ways:

•DANGER

• WARNING

•CAUTION

When a hazard is present that can cause pr operty da mag e, but ha s absol utely no pe rson al injur y risk,

a NOTICE is used.

DANGER IS USED TO INDICATE THE PRESENCE OF A HAZARD THAT WILL CAUSE SEVERE PERSONAL INJURY OR DEATH OR SUBSTANTIAL PROPERTY DAMAGE IF THE INSTRUCTIONS ARE IGNORED.

WARNING IS USED TO INDICATE THE PRESENCE OF A HAZARD THAT MAY CAUSE SEVERE PERSONAL INJURY OR SUBSTANTIAL PROPERTY DAMAGE IF INSTRUCTIONS ARE IGNORED.

CAUTION IS USED TO INDICATE THE PRESENCE OF A HAZARD THAT WILL OR CAN CAUSE MINOR PERSONAL INJURY OR 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 ofte n save you time or effort.

1-6 Section 1-1 - Overview

TAG

EYE

PROTECTION

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

1-3-2 Standard Hazard Icons

Important information will always be preceded by 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 cause harm. Even if a symbol isn’t used in this manual, it may be include d for your reference.

Table 1-3 Standard Hazard Icons

ELECTRICAL MECHANICAL RADIATION

LASER HEAT PINCH

Other hazard icons make you aware of specific procedures that should be followed.

NOTE: The Vivid™ S60/Vivid™ S70 system has no unintended or motorized moving parts that could cause

pinching; all moving parts are mechanically operated by the user. Pay attention to move such parts carefully (e.g. LCD arm).

Table 1-4 Standard Icons Indicating a Special Procedure Be Used

AVOID STATIC ELECTRICITY TAG AND LOCK OUT WEAR EYE PROTECTION

HAND PROTECTION FOOT PROTECTION

Chapter 1 - Introduction 1-7

PRELIMINARY

DANGER

WARNINGWARNING

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Section 1-4 Safety Considerations

1-4-1 Introduction

The following safety precautions must be observed duri ng 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.

1-4-2 Human Safety

• Operating personnel must not rem ove the Ultrasound system covers.

• Servicing should be performed by authorized personnel only.

• Only personnel who have participated in a Vivid™ S60/Vivid™ S70 Training Seminar are authorized to service the equipment.

NOTE: United States law restricts this device for sale or use by or on the order of a physician.

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 VIVID™ S60/VIVID™ S70 SYSTEM, SOME METAL SURFACES MAY BE WARM ENOUGH TO POSE A POTENTIAL HEAT HAZARD IF TOUCHED, EVEN WHILE IN SHUT DOWN MODE.

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.

HAVE TWO PEOPLE AVAILABLE TO DELIVER AND UNPACK THE VIVID™ S60/VIVID™ S70 SYSTEM. ATTEMPTS TO MOVE THE UNIT CONSIDERABLE DISTANCES OR ON AN INCLINE BY ONE PERSON COULD RESULT IN INJURY OR DAMAGE OR BOTH.

USE ALL PERSONAL PROTECTION EQUIPMENT (PPE) SUCH AS GLOVES, SAFETY SHOES, SAFETY GLASSES, AND KNEELING PAD, TO REDUCE THE RISK OF INJUR Y.

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, DO NOT

INSTALL SUBSTITUTE PARTS OR PERFORM ANY UNAUTHORIZED MODIFICATION OF THE EQUIPMENT.

1-8 Section 1-1 - Overview

WARNINGWARNING

CAUTION

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

WHEN THE TOP CONSOLE IS IN ITS LOCKED POSITION, THE GAS SHOCK IS COMPRESSED AND STORES MECHANICAL ENERGY. DURING NORMAL OPERATION, THE TOP CONSOLE, THE WEIGHT OF THE MONITOR AND THE MECHANICAL FORCE OF THE GAS SHOCK ARE IN BALANCE. TAKE CARE IF/ WHEN YOU ACTIVATE THIS GAS SHOCK. PERSONAL INJURY CAN OCCUR AFTER THE PANEL IS REMOVED AND THE SHOCK PRESSURE IS RELEASED. TAKE CARE WHEN YOU REPAIR THE ELEVATION ASSEMBLY.

USE PROTECTIVE GLASSES DURING DRILLING, FILING AND DURING ALL OTHER WORK WHERE EYES NEED PROTECTION.

USE SAFETY SHOES WHEN DOING WORK WHERE THERE IS ANY CHANCE OF FOOT DAMAGE.

USE PROTECTIVE GLOVES WHEN DRILLING AND CUTTING.

Chapter 1 - Introduction 1-9

PRELIMINARY

WARNINGWARNING

DANGER

CAUTION

WARNINGWARNING

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

1-4-3 Mechanical Safety

WHILE THE SOFTWARE INSTALL PROCEDURE IS DESIGNED TO PRESERVE DATA, YOU SHOULD SAVE ANY PATIENT DATA, IMAGES, SYSTEM SETUPS TO A DVD OR HARDCOPY BEFORE DOING A SOFTWARE UPGRADE.

PRIOR TO ELEVATING SCANNER, VERIFY THAT THE MONITOR IS LOCKED IN ITS LOWEST POSITION. VERIFY THAT THE FRONT BRAKE IS LOCKED AND THE SCANNER IS UNABLE TO SWIVEL. VERIFY THAT THE REAR BRAKES ARE IN THE LOCKED POSITION.

WHENEVER THE UNIT IS TO BE MOVED ALONG ANY INCLINE, USE EXTREME CAUTION. MAKE SURE THAT THE VIVID™ S60/VIVID™ S70 SCANNER AND ALL PERIPHERALS ARE SECURELY MOUNTED IN PLACE BEFORE ATTEMPTING TO MOVE IT.

ULTRASOUND PROBES ARE HIGHLY SENSITIVE MEDICAL INSTRUMENTS THAT CAN EASILY BE DAMAGED BY IMPROPER HANDLING. USE CARE WHEN HANDLING AND PROTECT FROM DAMAGE WHEN NOT IN USE. DO NOT USE A DAMAGED OR DEFECTIVE PROBE. FAILURE TO FOLLOW THESE PRECAUTIONS CAN RESULT IN SERIOUS INJURY AND EQUIPMENT DAMAGE.

NEVER USE A PROBE THAT HAS FALLEN TO THE FLOOR. EVEN IF IT LOOKS OK, IT MAY BE DAMAGED.

The Vivid™ S60/Vivid™ S70 ultrasound scanner weighs 7 5k g (1 65 lb s.) o r more , depe nding on carry-on peripherals when ready for use. Care must be used when moving the unit or replacing its parts. Failure to follow the precautions listed could result in injury, uncontrolled motion and costly damage. ALWAYS:

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

• Use the handle to move the system

• B e su re th e pat h wa y is cle ar

• Use slow, careful motions

• Do not let the system strike walls or door frames

• When moving the system on inclines, make sure that the Vivid™ S60/Vivid™ S70 scanner and all peripherals are securely mounted in place before attempting to move the scanne r.

• The rear handle should only be used for pushing the system. Do NOT use it for pulling the ultrasound scanner (in any direction) as this may ca use the system to become unstable in the event of colliding with obstacles

THE SYSTEM SHOULD NOT BE MOVED WITH THE OPERATING PANEL EXTENDED. POSITION THE OPERATING PANEL IN ITS CENTERED AND LOCKED POSITION. LOWER THE OPERATING PANEL AS MUCH AS POSSIBLE BEFORE MOVING THE SYSTEM. See Figure 5-7 on page 5-10 illustrating system in Transportation Mode.

REMEMBER: IF THE FRONT CASTER SWIVEL LOCK IS ENGAGED FOR TRANSPORTATION, PRESSING THE RELEASE PEDAL ONCE DISENGAGES THE SWIVEL LOCK. YOU MUST DEPRESS THE RELEASE PEDAL A SECOND TIME TO ENGAGE THE BRAKE.

1-10 Section 1-1 - Overview

CAUTION

WARNINGWARNING

CAUTION

WARNINGWARNING

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

BEFORE YOU MOVE OR TRANSPORT THE SYSTEM, MAKE SURE TO LOCK THE LCD MONITOR ARM FIRMLY AND FLIP DOWN THE MONITOR TO PREVENT DAMAGE TO THE SYSTEM.

See Figure 5-7 on page 5-10 illustrating system in Transportation Mode.

ALWAYS LOCK THE TOP CONSOLE (OPERATOR PANEL) IN ITS PARKING (LOCKED) POSITION BEFORE MOVING THE SCANNER AROUND.

TO AVOID INJURY WHEN YOU MOVE THE LCD MONITOR AND THE MONITOR ARM, DO NOT PUT YOUR FINGER, HAND, OR OBJECT ON THE JOINT OF THE MONITOR OR THE MONITOR ARM.

ENSURE THAT NO-ONE TOUCHES THE CONSOLE ARM/FROGLEG WHEN MOVING THE OPERATOR PANEL.

DO NOT MOVE THE UNIT IF THE OPERATOR PANEL IS IN UNLOCKED POSITION.

KEEP THE HEAT VENTING HOLES ON THE MONITOR UNOBSTRUCTED TO AVOID OVERHEATING OF THE MONITOR.

ALWAYS:

DO NOT TRANSPORT THE VIVID™ S60/VIVID™ S70 SYSTEM IN A VEHICLE WITHOUT LOCKING THE CASTERS (WHEELS)

See Figure 5-7 ON PAGE 5-10 illustrating system in Transportation Mode.

EQUIPMENT DAMAGE COULD RESULT IF SPECIAL CARE IS NOT TAKEN WHEN TRANSPORTING THE

VIVID™ S60/VIVID™ S70 SYSTEM IN A VEHICLE.

See Figure 5-7 on page 5-10 illustrating system in Transportation Mode.

• Eject any media from the media storage devices DVD, MOD (if installed).

• Ensure that monitor is in folded and locked position.

• Ensure that the Vivid™ S60/Vivid™ S70 system is well prepared and packed in its original packaging before transporting. Special care must be taken to correctly posit ion the packing material, using all screws and brackets. For further information, refer to Chapter 3 - System Setup.

• Place the probes in their carrying case.

• Secure the system in an full down position and lock the wheels (brake).

• Ensure that the Vivid™ S60/Vivid™ S70 system is firmly secured while inside the vehicle.

• Secure the 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.

ALWAYS LOCK THE SYSTEM IN ITS PARKED (LOCKED) POSITION AFTER MOVING. FAILURE TO DO SO COULD RESULT IN PERSONAL INJURY OR EQUIPMENT DAMAGE.

Chapter 1 - Introduction 1-11

PRELIMINARY

WARNINGWARNING

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

1-4-4 Electrical Safety

To minimize shock hazard, the equipment must be connected to a well grounded power source. The system is equipped with a three-conductor AC power cable. This must be plugged into an approved electrical outlet with safety grounding.

To ensure proper grounding, connect this equipment to a receptacle marked “HOSPITAL ONLY” OR “HOSPITAL GRADE”.

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 inte rnational electrical standards.

CONNECTING A VIVID™ S60/VIVID™ S70 SCANNER TO INCORRECT VOLTAGE LEVEL WILL DESTROY THE SYSTEM! CONNECT THE SYSTEM ONLY IN ACCORDANCE WITH THE VOLTAGE INDICATED ON THE PRODUCT LABEL.

1-4-4-1 Probes

All the probes for the Vivid™ S60/Vivid™ S70 ultrasound system are designed and manufactured to provide trouble-free, reliable service. To ensure this, correct handling of probes is important and the following points should be noted:

• Do not drop a probe or strike it against a ha rd surface, as this may damage the transducer elements, acoustic lens, or housing.

• Do not use a cracked or damaged probe. In this event, call your field service representative immediately to obtain a replacement.

• Avoid pulling, pinching or kinking the probe cable, since a damaged cable may compromise the electrical safety of the probe.

• To avoid the risk of a probe accidentally falling, do not allow the probe cables to become entangled, or to be caught in the system’s wheels.

Follow these guidelines before connecting a probe to the scanner:

• Inspect the probe prior to each use for damage or degradation to the:

- housing

- cable strain relief

-lens

- seal

- connector pins

- locking mechanism

• Do not use a damaged or defective probe.

• Never immerse the probe connector or adapter into any liquid.

• The system has more than one type of probe port. Use the appropriate pro be port designed for the probe you are connecting.

NOTE: For detailed information on handling endocavity probes, refer to the appropriate supplementary

instructions for each probe. In addition, refer to the Vivid™ S60/Vivid™ S70 User Manual for detailed probe handling instructions.

1-12 Section 1-1 - Overview

WARNINGWARNING

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

1-4-4-2 Peripherals

1-4-4-2-1 Safety and Environmental Guidelines

Environmental Dangers All devices meeting IEC60950 must be kept outside the patient environment as defined

in IEC60601-1 Clause 16, unless the devices, according to IEC60601-1 Clause 16, are equipped with the following:

A) Additional fixed earth protection or:

B) An extra isolating transformer

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 the provision of extra protective earth for the device, is required in order to meet IEC60601-1 Clause 16 standards for electrical leakage.

• Patient Environment EN 60601-1 Sub clause 3.79 - Patient Environment

It is difficult for this standard to define dimensions for the volume in which diagnosis, monitoring or treatment occurs. The dimensions for the PATIENT ENVIRONMENT given in Figure 1-1 have be en

justified in practice.

Figure 1-1 Example of Patient Environment

Chapter 1 - Introduction 1-13

PRELIMINARY

CAUTION

WARNINGWARNING

CAUTION

WARNINGWARNING

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

1-4-5 Vivid™ S60/Vivid™ S70 Battery Safety (part of Power Supply)

NOTE: The Vivid™ S60/Vivid™ S70 ultrasound scanner is supplied with a lith ium ion battery in the battery bay,

as an option.

The lithium ion battery provides power for safely shutting down the system or placing it in Standby mode, when an AC power source is interrupted or the AC power cable is disconnected from the wall outlet. Lithium ion batteries last longer than conventional batteries and do not require replacement as often. In Standby mode, you can expect 4 hours of battery life with a fully-charged battery.

Used batteries should not be placed with common household waste products. Contact local authorities for the location of a chemical waste collection program nearest you.

NOTE: Regulations vary for different countries. Dispose of a used battery in accordance with local regulat ions.

USE ONLY BATTERIES APPROVED BY GE AS SUITABLE FOR USE WITH THE VIVID™ S60/ VIVID™ S70 ULTRASOUND SCANNER

The Vivid™ S60/Vivid™ S70 battery is an approved UL device. DO NOT ATTEMPT TO DIS-ASSEMBLE OR ALTER THE BATTERY! Always observe the following precautions:

• 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 temperatures over 60 other heat sources.

• Do not leave the battery in direct sunlight.

• Do not pierce the battery with a sharp object, hit it, or step on it.

• Do not use a damaged battery.

• Do not apply solder to a battery.

• Do not connect the battery to an electrical power outlet.

TO PREVENT THE BATTERY BURSTING, IGNITING, OR FUMES FROM THE BATTERY CAUSING EQUIPMENT DAMAGE, ALWAYS OBSERVE THE FOLLOWING PRECAUTIONS:

• Do not immerse the battery in water or allow it to get wet.

• Do not place 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 appea rs abnormal during use, or system storage, immediately remove it and stop using it.

• If you have any questions about the battery, consult your local GE representative.

C (140o F). Keep the battery away from fire and

1-4-6 Patient Data Safety

WHILE THE SOFTWARE INSTALL PROCEDURE IS DESIGNED TO PRESERVE DATA, YOU SHOULD SAVE ANY PATIENT DATA, IMAGES, SYSTEM SETUPS TO A DVD OR HARDCOPY BEFORE DOING A SOFTWARE UPGRADE.

1-14 Section 1-1 - Overview

DANGER

WARNINGWARNING

DANGER

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Section 1-5 Dangerous Procedure Warnings

Warnings, such as the examples 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 VIVID™ S60/VIVID™ S70 SYSTEM, SOME METAL SURFACES MAY BE WARM ENOUGH TO POSE A POTENTIAL HEAT HAZARD IF TOUCHED, EVEN WHILE IN SHUT DOWN MODE.

EXPLOSION WARNING DO NOT OPERATE THE EQUIPMENT IN AN EXPLOSIVE ATMOSPHERE. OPERATION OF ANY ELECTRICAL EQUIPMENT IN SUCH AN ENVIRONMENT

CONSTITUTES A DEFINITE SAFETY HAZARD. EQUIPMENT IS NOT SUITABLE FOR USE IN THE PRESENCE OF A FLAMMABLE

ANAESTHETIC MIXTURE WITH AIR OR WITH OXYGEN OR NITROUS OXIDE.

DO NOT SUBSTITUTE PARTS OR MODIFY EQUIPMENT

BECAUSE OF THE DANGER OF INTRODUCING ADDITIONAL HAZARDS, DO NOT INSTALL SUBSTITUTE PARTS OR PERFORM ANY UNAUTHORIZED MODIFICATION OF THE EQUIPMENT.

Chapter 1 - Introduction 1-15

PRELIMINARY

NOTICE

Signed

Date

TAG

LOCKOUT

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Section 1-6 Lockout/Tagout (LOTO) Requirements

Follow OSHA Lockout/Tagout requirements (USA) or local Lockout/Tagout requirements by ensuring you are in total control of the AC power plug at all times. This will protect service personnel from injuries caused by unexpected energizing or start-up of equipment during service, repair, or maintenance.

To apply Lockout/Tagout (LOTO):

1.) Plan and prepare for shutdown .

2.) Shutdown the equipment.

3.) Isolate the equipment.

4.) Apply Lockout/Tagout Devices.

5.) Control all stored and residual energy.

6.) Verify isolation.

All potentially hazardous stored or residual energy is relieved.

ENERGY CONTROL AND POWER LOCKOUT FOR VIVID™ S60/VIVID™ S70. WHEN SERVICING PARTS OF THE SYSTEM WHERE THERE IS EXPOSURE TO VOLTAGE GREATER THAN 30 VOLTS:

1.) TURN OFF THE BREAKER.

2.) UNPLUG THE SYSTEM.

3.) MAINTAIN CONTROL OF THE SYSTEM POWER PLUG.

4.) 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. BEWARE THAT THE MAIN POWER SUPPLY AND BACK END PROCESSOR MAY BE ENERGIZED EVEN IF THE POWER IS TURNED OFF WHEN THE CORD IS STILL PLUGGED INTO THE AC OUTLET.

1-16 Section 1-1 - Overview

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Section 1-7 Product Labels and Icons

The Vivid™ S60/Vivid™ S70 ultrasound scanner comes equipped with product labels and icons. These represent pertinent information regarding the operation of the unit.

1-7-1 Universal Product Labels

NOTE: The following diagrams illustrate the labels found on the Vivid™ S60/Vivid™ S70 ultrasound unit. For

an explanation of label icons and symbols, refer to Table 1-7 on page 1-21 .

1-7-1-1 System Rating Label

A system Rating Label (examples shown below) is located at the rear of the system. This indicates the ultrasound system’s basic power compliance.

Table 1-5 Rating Label 1 of 3

Item # Description Illustration

Rating Label - Vivid™ S60 (100-240V)

(with UDI code and new address)

International

(with Assembled in China)

International

Chapter 1 - Introduction 1-17

PRELIMINARY

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Table 1-5 Rating Label (Continued) 2 of 3

Item # Description Illustration

Rating Label - Vivid™ S60 (100-240V)

International

Rating Label - Vivid™ S70 (100-240V)

International

(with Assembled in China)

Rating Label - Vivid™ S70 (100-240V)

International

(with UDI code and new address)

1-18 Section 1-1 - Overview

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Table 1-5 Rating Label (Continued) 3 of 3

Item # Description Illustration

Rating Label - Vivid™ S70 (100-240V)

International

Chapter 1 - Introduction 1-19

PRELIMINARY

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

1-7-1-2 General Label

A General Label (below) provides details regarding regulatory compliance - as well as warnings and cautions.

Table 1-6 General Label

Item # Description Illustration

General Label - International

(with new address)

General Label - International (with EAC,

GOST and TÜV SÜD mark)

General Label - International

1-20 Section 1-1 - Overview

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

1-7-2 Label Descriptions

The following table shows the labels and symbols that may be found on the Vivid™ S60/Vivid™ S70 ultrasound system, and provides a description of each label’s purpose and location.

Table 1-7 Label Icons and Symbols - Description and Location

Label Name Purpose Location Standard

Manufacturer’s name and address. Identification and Rating Plate

Date of Manufacture.

Model and Serial numbers.

Electrical ratings (Volts, Amps, phase, and frequency.

On/Off button

Warning: System shutdown using the On/Off button

does not disconnect the ultrasound system from

mains voltage.

For disconnecting the ultrasound system from mains

voltage after system shutdown, please set the circuit

breaker close to the mains inlet to OFF , see: Figure 4-4 on

page 4-5.

Equipment Type BF, in which protection against electric

shock does not rely on basic insulation only. Provides

additional safety precautions such as double insulation or

reinforced insulation, because there is no provision for

protective earthing or reliance upon installation

conditions.

Rear of the system.

Control panel IEC 60417-5010

Rear of system. Probes.

IEC 60417-5333

Defibrillator-proof Type CF equipment ECG connector IEC 60417-5336

CE certification mark. Indicates that the product is in

compliance with all relevant European Directives, and

under surveillance by Notified Body 0459.

Indicates the Vivid™ S60/Vivid™ S70 is a UL-approved

system (InMetro Brazil).

TUV Rheinland of North America, Inc.

TUV SÜD

Classification Label

Rear of the system.

Rear of the system (Identification plate)

N/A- by certification body

Chapter 1 - Introduction 1-21

PRELIMINARY

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Table 1-7 Label Icons and Symbols - Description and Location (Continued)

Label Name Purpose Location Standard

Mark name: "Eurasian Conformity" mark; the single conformity mark for circulation of products on the markets of member- states of Customs Union.

Mark meaning: This product passed all conformity assessment (approval) procedures that correspond to the requirements of applicable technical reguations of the Customs Union.

GOST-R Mark: per Law of the Russian Federation No. 184-FZ.

Non-ionizing electromagnetic radiation.

Rear of the system.

Rear of system. N/A- by certification body

Rear of system. IEC 60417-5140

N/A- by certification body

Alternating current Various IEC 60417-5032

Protective earth (ground) Internal IEC 60417-5019

Equipotentiality: Indicates the terminal to be used for connecting equipotential conductors when interconnecting (grounding) with other equipment.

Follow instructions for use. Read and understand all instructions in the User's Manual before attempting to use the ultrasound system.

Symbol indicating that the Instructions for Use are supplied in electronic form.

Peripherals. IEC 60417-5021

Rear of the system.

Rear of system. ISO 7000-1641

ISO 7010-M002

CAUTION - Dangerous voltage: Used to indicate electric shock hazards.

1-22 Section 1-1 - Overview

Rear of system. Various.

ISO 7010-W012

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Table 1-7 Label Icons and Symbols - Description and Location (Continued)

Label Name Purpose Location Standard

Attention - Consult accompanying documents: Alerts the

user to refer to the user documentation when complete

information cannot be provided on the label.

Various. ISO 7010-W001

The system is not designed for use with flammable

anesthetic gases.

CAUTION - Do not push the system sideways when

casters are in break position. Instability may occur.

DO NOT place objects on the surface of the rear of the

LCD Panel while folded.

This symbol indicates that 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.

The disassembly and parts disposition procedure is

located on the card cage front cover. To access to the

procedure, remove the right side panel.

System weight Rear of system N/A- by GE Healthcare

Rear of system N/A- by GE Healthcare

Top console (both sides).

Display rear panel.

Rear of system. EN 50419

ISO 7010-P017

ISO 7010-P012

Date of manufacture: The date could be a year, year and

month, or year, month and day, as appropriate. See ISO

8601 for date formats.

Manufacturer name and address Rear of system. ISO 7000-3082

Serial number.

Brand and model identifier Rear of system. ISO 7000-3082

Device part number identifier Rear of system N/A- by GE Healthcare

For USA only:

Caution: Federal law restricts this device to sale by or

on the order of a licensed healthcare practitioner.

Rear of system. ISO 7000-2497

Rear of the system.

ISO 7000-2498

Chapter 1 - Introduction 1-23

PRELIMINARY

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Table 1-7 Label Icons and Symbols - Description and Location (Continued)

Label Name Purpose Location Standard

Precaution intended to prevent injury that may be caused by the weight of the system if one person attempts to move it considerable distances, or on an incline.

Service documentation

N/A- by GE Healthcare

1-24 Section 1-1 - Overview

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

1-7-3 Vivid™ S60/Vivid™ S70 External Labels

In addition to the labels described in the previous section, an additional label may be found on the Vivid™ S60/Vivid™ S70 ultrasound system, as described in the following section.

1-7-3-1 GND Label

Indicates the protective earth (grounding) terminal. The GND label (Figure 1- 2 below) is located at the rear of the system.

Figure 1-2 GND Label

Chapter 1 - Introduction 1-25

PRELIMINARY

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Section 1-8 Returning/Shipping Probes and Repair Parts

Equipment being returned must be clean and free of blood and other in fectious 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 th at 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 purpo ses 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 Vivid™ S60/Vivid™ S70 ultrasound scanner is not meant to be used for long-term storage of patien t data or images. The user is responsible for the data on the Vivid™ S60/Vivid™ S70 and a regular backup is highly recommended.

If the Vivid™ S60/Vivid™ S70 is sent for repair, ensure that any patient information is backed up and erased from the Vivid™ S60/Vivid™ S70 before shipping. It is always possible d uring 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 wher e 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.

1-26 Section 1-8 - Returning/Shipping Probes and Repair Parts

WARNINGWARNING

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Section 1-9 EMC, EMI, and ESD

1-9-1 Electromagnetic Compatibility (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 to interference from its environment, or when the device produces unacceptable levels of emission. This interference is often refe rred to as radio–frequency or electromagnetic interference (RFI/EMI) and can be radiated through space or conducted over interconnecting power or 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.

NOTE: The Vivid™ S60/Vivid™ S70 ultrasound scanner needs special precautions regarding EMC an d needs

to be installed and put into service according to the EMC information provided in the accompanying documents (supplied with the system).

NOTE: Portable and mobile RF communications equipment can affect the Vivid™ S60/Vivid™ S70 ultrasound

scanner.

THE USE OF ACCESSORIES, TRANSDUCERS AND CABLES OTHER THAN THOSE SPECIFIED, WITH THE EXCEPTION OF TRANSDUCERS AND CABLES SOLD BY THE MANUFACTURER OF THE VIVID™ S60/VIVID™ S70 AS REPLACEMENT PARTS FOR INTERNAL COMPONENTS, MAY RESULT IN INCREASED EMISSIONS OR DECREASED IMMUNITY OF THE VIVID™ S60/VIVID™ S70.

THE VIVID™ S60/VIVID™ S70 SHOULD NOT BE USED ADJACENT TO OR STACKED WITH OTHER EQUIPMENT AND THAT IF ADJACENT OR STACKED USE IS NECESSARY, THE VIVID™ S60/VIVID™ S70 SHOULD BE OBSERVED TO VERIFY NORMAL OPERATION IN THE CONFIGURATION IN WHICH IT WILL BE USED.

1-9-2 CE Compliance

The Vivid™ S60/Vivid™ S70 ultrasound scanner 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.

NOTE: For applicable standards refer to the Safety Chapter in the Vivid™ S60/Vivid™ S70 User Manual. NOTE: For EMC Guidance and Manufacturer’s Declarations, refer to the tables provided in Electrostatic

Discharge (ESD) Prevention on page 1 - 28.

NOTE: For CE Compliance, it is critical that all covers, screws, shielding, gaskets, mesh and clamps are in good

condition and 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.

Chapter 1 - Introduction 1-27

PRELIMINARY

WARNINGWARNING

CAUTION

WARNINGWARNING

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

1-9-3 Electrostatic Discharge (ESD) Prevention

DO NOT TOUCH ANY BOARDS WITH INTEGRATED CIRCUITS PRIOR TO TAKING THE NECESSARY ESD PRECAUTIONS:

1.ALWAYS CONNECT YOURSELF, VIA AN ARM-WRIST STRAP CONNECTED TO THE CAGE ASSEMBLY OR ANY GROUND SCREW WHENEVER YOU OPEN THE SYSTEM FOR MAINTENANCE.

2.FOLLOW GENERAL GUIDELINES FOR HANDLING OF ELECTROSTATIC SENSITIVE EQUIPMENT.

RISK OF ELECTRICAL SHOCK, 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.

1-9-4 General Caution

Any changes to accessories, peripheral units or any other part of the system must be approve d by the manufacturer. Ignoring this advice may compromise the regulatory approvals obtained for the product.

IF THE COVERS ARE REMOVED FROM AN OPERATING VIVID™ S60/VIVID™ S70, SOME METAL SURFACES MAY BE WARM ENOUGH TO POSE A POTENTIAL HEAT HAZARD IF TOUCHED, EVEN WHILE IN SHUTDOWN MODE.

1-28 Section 1-8 - Returning/Shipping Probes and Repair Parts

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Section 1-10 Customer Assistance

1-10-1 Contact Information

If this equipment does not operate as indicated in this Se rvice Manual or in the Vivid™ S60/Vivid™ S70 User Manual, or if you require additional assistance, please contact the local distributor or appropriate

support resource, as listed below. Prepare the following information before you call:

• Ultrasound System ID and/or serial number.

• Software version.

• Date and time of occurrence.

• Sequence of events leading to issue.

• Is the issue reproduceable?

• Imaging mode, probe, preset/application.

• Media brand, speed, capacity, type.

• Save secondary image capture, cine loop, 4D multi-volume loop.

• Detailed description of any problem encountered.

NOTE: Restart the application before resuming clinical scanning.

1-10-1-1 Phone Numbers for Customer Assistance

Table 1-8 Phone Numbers for Customer Assistance

1-30 Section 1-8 - Returning/Shipping Probes and Repair Parts

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

1-10-1-2 Phone and Fax Numbers for Manufacturer

Table 1-9 Phone and Fax Numbers for Manufacturer

MANUFACTURER PHONE NUMBER FAX NUMBER

GE Medical Systems, Israel Ltd. Nativ Ha'or Street no. 1 3508510 Haifa ISRAEL

+972-4-8519555 +972-4-8519500

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PRELIMINARY

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

This page was intentionally left blank.

1-32 Section 1-8 - Returning/Shipping Probes and Repair Parts

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Chapter 2

Site Preparations

Section 2-1 Overview

2-1-1 Purpose of Chapter 2

This chapter provides the information required to plan and prepare for the setup of a Vivid™ S60 or Vivid™ S70 ultrasound system. Included are descriptions of the electrical and facility requir ements that must be met by the purchaser. A worksheet is provided at the end of this chapter (see Figure 2-5 on page 2-13) to help ensure that all the required network information is available, prior to setup.

2-1 Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-1

2-2 Console Requirements. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-2

2-3 Facility Needs. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-6

2-4 Connectivity Installation Worksheet . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-13

Chapter 2 - Site Preparations 2-1

PRELIMINARY

CAUTION

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Section 2-2 Console Requirements

2-2-1 Unit Environmental Requirements

2-2-1-1 Environmental Requirements - v203

Table 2-1 Environmental Requirements - v 203

Relative Humidity

Requirement Temperature

(non-condensing)

Air Pressure

Operational

Storage

Transport

+10 — +35

-20 — +60

C (50 — 95oF)

C (-4 — 140oF)

C (-4 — 140oF))

30 — 85% 700 — 1060 hPa

10 — 95% 700 — 1060 hPa

10 — 95% 700— 1060 hPa

NOTE: The Vivid™ S60/Vivid™ S70 system may be operated at an altitude of up to 3000 meters (9842 ft).

IF THE SYSTEM HAS BEEN IN STORAGE OR HAS BEEN TRANSPORTED, PLEASE SEE THE ACCLIMATION REQUIREMENTS BEFORE POWERING ON AND/OR USING THE SYSTEM. Refer to the Setup Warnings section on page 3-2.

NOTE: After a long period of storage, or after transportation of the system with the monitor in the folded-down

position (transportation mode), it is highly recommended to place the monitor in the upright position and to leave it in this position for a period of longer than 1 hour before use. This will enable it to properly adjust to the environmental conditions.

2-2-2 Cooling Requirements

The cooling requirement for the Vivid™ S60/Vivid™ S70 ultrasound system environment is 2000 BTU/ hr. This figure does not include the cooling required for lights, people, or other equipment in the room.

Note: Each person in the room places an additional 300 BTU/hr demand on the environmental cooling.

2-2-3 Lighting Requirements

For system setup, updates and repairs, bright lighting is required. However, operator and patient comfort may be optimized if the room lighting is subdued and indirect when a scan is being per formed. Therefore, a combination lighting system (dim/bright) is recommended.

2-2-4 Time and Manpower Requirements

Site preparation takes time. Begin pre-setup checks as soon as possible to allow sufficient time to make any required changes. If possible, begin these checks as many as six weeks before system delivery.

Only one person is required to unpack the Vivid™ S60/Vivid™ S70 ultrasound system; at least two people must be available to roll the system down the wheeling ramp. Attempts to move the system considerable distances (or on an incline) by

one person alone, could result in personal injury, and/or damage to the system.

2-2 Section 2-2 - Console Requirements

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

2-2-5 Electrical Requirements

NOTE: GE requires a dedicated mains power line and Grou nd for the proper operation of its Ultrasound

equipment. This dedicated power line shall originate at the last distribution panel before the 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 unit is only a conduit.

2-2-5-1 Vivid™ S60/Vivid™ S70 Power Requirements

Electrical specifications for the Vivid™ S60/Vivid™ S70 system are as follows:

Table 2-2 Electrical Requirements

Input Voltage Tolerances Op. Current Frequency

100V AC to 240V AC ±10% 500VA 50-60 Hz

2-2-5-2 Inrush Current

Inrush current is not a factor for consideration, due to the inrush current limiting prop erties of the power supplies.

Table 2-3 Inrush Current

Voltage

100 V 4.5 A 240 V 2.3 A

2-2-5-3 Site Power Outlets

A dedicated AC power outlet must be within reach of the unit without requiring the use of extension cords. Other outlets adequate for the external peripherals, medical and test equipment required to support this unit must also be present and located within 1 m (3.2 ft) of the unit. Electrical installation must meet all current local, state, and national electrical codes.

2-2-5-4 Mains Power Plug

The Vivid™ S60/Vivid™ S70 portable ultrasound scanner is supplied with an AC power cable , as standard. In the event that the unit arrives withou t a po we r cab le , or a po we r cab le fitted w ith an incorrect plug, contact your GE dealer. When necessary, the installation engineer will supply the appropriate power plug to meet the applicable local regulations.

Inrush Current

(Console Only)

Chapter 2 - Site Preparations 2-3

PRELIMINARY

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

2-2-5-5 Power Stability Requirements

• Voltage drop-out

Max 10 msec

• Power Transients

The Vivid™ S60/Vivid™ S70 ultrasound scanner is fully compliant with the following standard: EN/IEC 60601-1-2.

2-2-6 EMI Limitations

Ultrasound machines are susceptible to Electromagnetic Interference (EMI) from radio frequencies, magnetic fields, and transients in the air or wiring. They also generate EMI. The Vivid™ S60/Vivid™ S70 ultrasound system complies with limits as stated on the EMC label. However, there is no guarantee that interference will not occur in a particular setup.

Note: Possible EMI sources should be identified before the unit is installed, and should not be on the

same line as the ultrasound system. A dedicated line sh ould be used for the ultrasound system. Electrical and electronic equipment may produce EMI unintentionally as the result of a defect. Sources

of EMI include the following:

• Medical lasers.

• Scanners.

• Cauterizing guns.

•Computers.

•Monitors.

•Fans.

• Gel warmers.

• Microwave ovens.

• Portable phones.

• Broadcast stations and mobile broadcasting machines.

2-4 Section 2-2 - Console Requirements

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

2-2-7 EMI Prevention/Abatement

The following table lists recommendations for preventing EMI:

Table 2-4 EMI Prevention/ Abatement

EMI Rule Details

Ground the unit.

Be aware of RF sources.

Replace and/or reassemble all screws, RF gaskets, covers and cores.

Replace broken RF gaskets.

Do not place labels where RF gaskets touch metal.

Use GE-specified harnesses and peripherals.

Take care with cellular phones.

Properly address peripheral cables.

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

Keep the unit at least 5m (16.4 ft) 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.

After you finish repairing or updating the system, replace all covers and tighten all screws. Any cable with an external connection requires a magnet wrap at each end. Install the shield over the front of the card cage. Loose or missing covers or RF gaskets allow radio frequencies to interfere with the ultrasound signals.

If more than 20% or a pair of the fingers on an RF gasket are broken, replace the gasket. Do not turn ON the unit until any loose metallic part is removed and replaced, if required.

Never place a label where RF gaskets meet the unit. Otherwise, the gap created will permit RF leakage. In case a label has been found in such a location, move the label to a different, appropriate location.

The interconnect cables are grounded and require ferrite beads and other shielding. Cable length, material, and routing are all important; do not make any changes that do not meet all specifications.

Cellular phones may transmit a 5 V/m signal that causes image artifacts.

Do not allow cables to lie across the top of the system. Loop any peripheral cable excess length into one bundle.

2-2-8 Probe Environmental Requirements

Table 2-5 Probe Operation and Storage Temperatures

Electronics

Operation Storage

Note: System and electronic probes are designed for storage temperatures of -20o to +50o C. When

exposed to large temperature variations, the probes should be kept at room temperature for a minimum of 10 hours before use.

10 — 40oC (50 — 104oF)

-20 — 50oC (-4 — 122oF)

Chapter 2 - Site Preparations 2-5

PRELIMINARY

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Section 2-3 Facility Needs

2-3-1 Purchaser Responsibilities

The work and materials required to prepare the site are the responsibility of the purchaser. To avoid delay, complete all pre-setup work before delivery. Use the Pre-setup Check List (provided in

Table 2-6 on page 2-15) to verify that all the required steps have been completed.

Purchaser responsibilities include:

• Procuring the required materials.

• Completing the preparations prior t o delive ry of the ult ra so un d sys te m.

• Paying the costs of any alterations and modifications not specifically provided for in the sales contract.

Note: All relevant preliminary electrical installations at the prepared site must be performed by

licensed electrical contractors. Other connections between electrical equipment, and calibration and testing, must also be performed by qualified personnel. The products involved (and the accompanying electrical installations) are h ighly 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 utilize only qualified personnel to perform electrical servicing of the equipment.

To avoid delays during setup, the individual or team who will perform the setup should be notified at the earliest possible date (preferably prior to setup), of the existence of any of the following variances:

• Use of any non-listed product(s).

• Use of any customer provided product(s).

• Placement of an approved product further from the system than the interface kit allows.

The prepared site must be clean prior to delivery of the system. Carpeting is not recomme nded because it collects dust and creates static. Potential sources of EMI should also be investigated before delivery. Dirt, static, and EMI can negatively impact system reliability.

2-6 Sect ion 2-3 - Facility Needs

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

2-3-2 Mandatory Site Requirements

The following are mandatory site requirements. Additional (optional) recommendations, as well as a recommended ultrasound room layout, are provided in section 2-3-3 - Site Recommendations (see below).

• A dedicated “hospital-grade” single branch power outlet of adequate amperage (see Table 2-2 on

page 2-3.) that meets all local and national codes and is located less than 2.5 m (8.2 ft) from the

unit’s proposed location. Refer to the Electrical Requirements section on page 2-3.

• A door opening of at least 0.54 m (1.77 ft) in width.

• The proposed location for the unit is at least 0.2 m (0.67 ft) from the walls, to enable cooling.

• Power outlet and place for any external peripheral are within 2 m (6.5 ft.) of each other with peripheral within 1 m of the unit to connect cables.

• Power outlets for other medical equipment and gel warmer.

• Power outlets for test equipment within 1 m (3.3 ft) of the ultrasound system.

• Clean and protected space for storage of probes (either in their case or on a rack).

• Material to safely clean probes (perform ed usin g a pla stic con tain e r, ne ve r me ta l).

• In the case of a network option:

• An active network outlet in the vicinity of the ultrasound system.

• A network cable of appropriate length (regular Pin-to-Pin network cable).

• An IT administrator who will assist in configuring the unit to work with your local network. A fixed

IP address may be required when using DICOM. Refer to the form provided in Figure 2-5 on page 2-13 for network details that are required.

Note: All relevant preliminary network outlets installations at the prepared site must be perform ed by

authorized contractors. The purchaser of GE equipment must utilize only qualified personnel to perform servicing of the equipment.

2-3-3 Site Recommendations

The following are (optional) site recommendations. Mandatory site requirements are provided in the

Mandatory Site Requirements section, above.

• Door opening of 92 cm (3 ft) in width.

• Accessible circuit breaker for a dedicated “hospital-grade” power outlet.

• Sink with hot and cold running water.

• Receptacle for bio–hazardous waste, for example, used probe sheaths.

• Emergency oxygen supply.

• Storage area for linens and equipment.

• Nearby waiting room, lavatory, and dressing room.

• Dual-level lighting (bright and dim).

• Lockable cabinet for software and manuals.

Chapter 2 - Site Preparations 2-7

PRELIMINARY

36 IN.

(92 CM)

Dedicated Power Outlets

Hospital Network

GE Cabinet for Software and Manuals (optional)

Vivid S60/70

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

2-3-3-1 Recommended Ultrasound Room Layout

Figure 2-1 below shows a floor plan illustrating the recommended layout of the Ultrasound Room and

depicting the minimal room layout requirements.

Figure 2-1 Recommended Floor Plan 4.3m x 5.2m (14 ft x 17 ft)

2-8 Sect ion 2-3 - Facility Needs

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

2-3-3-2 Minimal Floor Plan Suggestion

Scale:

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

1. Sink

2. Linens

3. Probes / supplies

Figure 2-2 Minimal Floor Plan - 2.5 m x 3 m (8 x 10 ft)

4. Ethernet Connector

5. Power outlet

6. Stool

7. Ultrasound system

8. GE cabinet for software and manuals (optional)

9. Examination table

10. Door (76 cm)

Chapter 2 - Site Preparations 2-9

PRELIMINARY

13 14

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

2-3-3-3 Recommended Floor Plan Suggestion

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

1. Secretaries or Doctors Desk

2. File Cabinet

3. Film Viewer

4. Counter Top

5. Counter Top and Sink with hot and cold water

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

7. Emergency Oxygen

Figure 2-3 Recommended Floor Plan - 4.27 x 5.18 m (14 x 17 ft)

8. Suction Line

9. Ultrasound system

10. Dedicated Power Outlet Circuit Breaker protected and easily accessible

11. Network Interface

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

13. Stool

2-10 Section 2-3 - Facility Needs

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)

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

2-3-3-4 Suggested Floor Plan with System and Workstation in Same Room

1. EchoPAC 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 2-4 Suggested Floor Plan with Workstation and Ultrasound System in Same Room

Chapter 2 - Site Preparations 2-11

PRELIMINARY

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

2-3-4 Networking Pre-Installation Requirements

2-3-4-1 Stand-alone Unit (without Network Connection)

None.

2-3-4-2 Scanner Connected to Hospital’s Network

Supported networks:

• Wireless LAN

• 10/100/1000 Mbps Ethernet/DICOM network

2-3-4-3 InSite™ requirements

Need internet access on the outbound port to GE’s remote service platform (InSite), which is only opened on request by the user and through a secure HTTPS connection on port 443.

InSite requires an Ethernet connection with a 10/100 Mbps or 10/100/1000 Mbps interface.

2-3-4-4 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 moni tor and peripherals, enabling viewing to be done while scanning continues. With DICOM, images can be archived, stored, and retrieved faster, easier, a nd at a lower cost.

2-3-4-5 DICOM Option Pre-Installation Requirements

To configure the Vivid™ S60/Vivid™ S70 ultrasound system to work with other network connections, the network administrator must provide the required information, which should include the following:

• Details: DICOM network details for the Vivid™ S60/Vivid™ S70 unit, including the host name, local port, IP address, AE title and net mask.

• Routing Information: IP addresses for the default gate way and other routers in use at the site.

• DICOM Application Information:Details of the DICOM devices in use at the site, including the DICOM host name, AE title and IP addresses.

2-12 Section 2-3 - Facility Needs

Site System Information

Services (Destination Devices)

TCP/IP Settings

Device Type

Manufacturer

Name

IP Address

Port

AE Title

1 2 3 4 5 6 7 8

9 10 11 12

Dept:

Vivid™ S60/ Vivid™ S70 SN:

Type:

Floor:

Room:

REV:

Comments:

CONTACT INFORMATION Name

Title

Phone

E-Mail Address

Site:

Scanner IP Settings

IP Address:

Subnet Mask:

Default Gateway:

(Echo Server/GEMNet Server/EchoPac PC)

Server Name:

Remote DB User Name:

Name - AE Title:

Remote Archive Setup

IP Address:

Subnet Mask:

Default Gateway:

Name - AE Title:

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Section 2-4 Connectivity Installation Worksheet

Figure 2-5 Connectivity Installation Worksheet

Chapter 2 - Site Preparations 2-13

PRELIMINARY

Vivid™ S60/Vivid™ S70 Host Name

AE Title

Local Port

IP Address

Net Mask

...

ROUTING INFORMATION

ROUTER2 ROUTER3

ROUTER1

...

... ... ...

Destination IP Addresses

GATEWAY IP Addresses

Default

DICOM APPLICATION INFORMATION

NAME

Store 2

Store 3

Store 1

MAKE/REVISION IP ADDRESSES PORTAE TITLE

Store 5

Store 6

Store 4

Storage Commit

MPPS

Work list

...

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Figure 2-6 Worksheet for DICOM Network Information

2-14 Section 2-4 - Connectivity Installation Worksheet

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Table 2-6 Vivid™ S60/Vivid™ S70 Pre-Setup Check List

Action Yes No

Schedule at least 3 hours for setup of the system.

Notify setup team of the existence of any variances from the basic setup.

Make sure system and probes have been subject to acclimation period.

Environmental cooling is sufficient.

Lighting is adjustable to adapt to varying operational conditions of the scanner.

Electrical facilities meet system requirements.

EMI precautions have been taken and all possible sources of interference have been removed.

Mandatory site requirements have been met.

If a network is used, IP address has been set for the system and a dedicated network outlet is available.

This page was intentionally left blank.

Chapter 2 - Site Preparations 2-15

PRELIMINARY

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

This page was intentionally left blank.

2-16 Section 2-4 - Connectivity Installation Worksheet

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Chapter 3

System Setup

Section 3-1 Overview

3-1-1 Purpose of Chapter 3

This chapter provides instructions for setting up the Vivid™ S60/Vivid™ S70 ultrasound system. Before beginning the setup process, an appropriate site must be prepared, as described in Chapter 2 - Site

Preparations. Once the site has been prepared, setup can proceed as described in this chapter.

Included in this chapter are guidelines for transporting the unit to a new site, as well as procedures that describe how to receive and unpack the equipment, and (if necessary) how to file a damage or loss claim. Instructions for checking and testing the unit, probes, and external peripherals for electrical safety are also provided.

NOTE: An ultrasound system is ready for use only if the tests and checks described in

Chapter 3 - System Setup (this chapter) and Chapter 4 - General Procedures and Functional Checks of this Service Manual meet the expected results.

3-1 Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-1

3-2 Setup Reminders . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-2

3-3 Receiving and Unpacking the Equipment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5

3-4 Preparing for Setup. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-21

3-5 Completing the Setup. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-26

3-6 Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-33

3-7 Connectivity Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-45

3-8 Connectivity Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-46

3-9 Options Setup. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-51

3-10 Paperwork After Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-75

Chapter 3 - System Setup 3-1

PRELIMINARY

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Section 3-2 Setup Reminders

3-2-1 Average Setup Time

The Vivid™ S60/Vivid™ S70 setup and functional checkout will take approximately one hour; Vivid™ S60/Vivid™ S70 consoles with optional equipment (such as Alphanumeric Keyboard) may take sligh tly longer.

Once the site has been prepared, the average installation time required is shown in Table 3-1 below.

Table 3-1 Average Setup Time

Average

Description

Setup Time

Comments

Unpacking the scanner Installing the scanner DICOM Option

(connectivity) Installing InSite

Encrypting the patient data

30 minutes 30 minutes Time may vary, according to the required configuration

30 minutes Time may vary, according to the required configuration

30 minutes

While the system is undergoing encryption, it will not be

Up to several hours

available for use. It is highly recommended to perform disk encryption overnight or when the system is not needed for use for an extended period of time.

3-2-2 Setup Warnings

1.) The Vivid™ S60/Vivid™ S70 ultrasound scanner weighs 75 kg (165 lbs), without add-ons/ peripherals. Two people are always required to unpack the system.

2.) There are no operator-serviceable components. To prevent shock, do not remove any covers or

panels. If problems or malfunctions occur, unplug the power cord. Only qualified service personnel should carry out servicing and troubleshooting.

NOTE: For information on shipping carton labels, refer to Figure 3-1 on page 3-6 and Figure 3-4 on

page 3-9.

3-2 Section 3-2 - Setup Reminders

CAUTION

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

3-2-2-1 System Acclimation Time

Following transport, the Vivid™ S60/Vivid™ S70 system may be very cold, or hot. Allow time for the

system to acclimate before being switched ON. Acclimation requires 1 hour for each 2 .5

when the temperature of the system is below 10

C or above 40oC.

C increment,

Turning the system ON after arrival at the site - without allowing time for acclimation - may cause system damage!

Table 3-2 Vivid™ S60/Vivid™ S70 System Acclimation Time

0 2.5 5 7.5 10 35 40 42.5 45 47.5 50 52.5 55 57.5 60

°C

32 36.5 41 45.5 50 95 104 108.5 113 117.5 122 126.5 131 135.5 140

°F

4321002 3 4 5 6 7 8 910

Hrs

NOTE: After a long period of storage, or after transportation of the system with the monitor in the folded-down

position, it is highly recommended to place the monitor in the upright position - and to leave it in this position for a period of longer than 1 hour before use. This will enable it to properly adjust to the environmental conditions.

Chapter 3 - System Setup 3-3

PRELIMINARY

DANGER

WARNINGWARNING

CAUTION

WARNINGWARNING

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

3-2-3 Safety Reminders

WHEN USING ANY TEST INSTRUMENT THAT IS CAPABLE OF OPENING THE AC GROUND LINE (I.E., METER’S GROUND SWITCH IS OPEN), DO NOT TOUCH THE UNIT!

TWO PEOPLE ARE REQUIRED TO UNPACK THE SYSTEM AS IT IS HEAVY. TWO PEOPLE ARE ALWAYS REQUIRED WHENEVER A PART WEIGHING 16KG (35 LB.) OR MORE MUST BE LIFTED.

IF THE UNIT IS VERY COLD OR HOT, DO NOT TURN ON POWER TO THE UNIT UNTIL IT HAS HAD SUFFICIENT TIME TO ACCLIMATE TO ITS OPERATING ENVIRONMENT.

TO PREVENT ELECTRICAL SHOCK, CONNECT THE UNIT TO A PROPERLY GROUNDED POWER OUTLET.

DO NOT USE A THREE-PRONG TO TWO-PRONG ADAPTER, AS THIS DEFEATS SAFETY GROUNDING.

DO NOT WEAR THE ESD WRIST STRAP WHEN YOU WORK ON LIVE CIRCUITS WHERE MORE THAN 30 V PEAK IS PRESENT.

DO NOT OPERATE THE UNIT UNLESS ALL BOARD COVERS AND FRAME PANELS ARE SECURELY IN PLACE, TO ENSURE OPTIMAL SYSTEM PERFORMANCE AND COOLING. (WHEN COVERS ARE REMOVED, EMI MAY BE PRESENT).

ACOUSTIC OUTPUT HAZARD ALTHOUGH THE ULTRASOUND ENERGY TRANSMITTED FROM THE Vivid™ S60/ Vivid™ S70 PORTABLE ULTRASOUND SCANNER IS WITHIN AIUM/NEMA STANDARDS AND FDA LIMITATIONS, AVOID UNNECESSARY EXPOSURE. ULTRASOUND ENERGY CAN PRODUCE HEAT AND MECHANICAL DAMAGE

Note: The Vivid™ S60/Vivid™ S70 User Manual should be fully read and understood before

operating the unit. Keep the manual near the unit for reference.

3-4 Section 3-2 - Setup Reminders

CAUTION

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Section 3-3 Receiving and Unpacking the Equipment

3-3-1 Warnings for Receiving and Unpacking the Equipment

Two people are needed to unpack the Ultrasound system because of its weight. Attempts to move the Ultrasound system considerable dist ances or on an incline by one person cou ld result in injury or damage or both.

Two people are required whenever a part weighing 16 KG (35 LBS) or more must be lifted.

Remember to use relevant personal protecting equipment (PPE) during packing and unpacking. Check with your local EHS representative.

3-3-2 Overview

Please read this section fully before unpacking the Vivid™ S60/Vivid™ S70 ultrasound system.

Depending on manufacturing site and transportation metho d used for shipp ing th e ul trasou nd syste m, a few different packagings may be used:

• Single cardboard shipping carton mounted on a raised wooden base

• Ocean shipping package (for some shipments to USA) The Vivid™ S60/Vivid™ S70 ultrasound system, together with the peripherals, probes, cables, and

accessories, are shipped from the factory in a single cardboard shipping carton mounted on a raised wooden base - see Figure 3-2 on page 3-7.

Unpacking instructions for each type of shipping carton are provided separately in the following sections:

• Unpacking the Vivid™ S60/Vivid™ S70 Scanner with Peripherals on page 3 - 10

• Unpacking the Vivid™ S60/Vivid™ S70 Scanner on page 3 - 10

• Unpacking the Ocean Shipping package on page 3 - 14

NOTE: For details of weights and dimensions of the shipping cartons, refer to Table 3-3 on page 3-8.

Each cardboard shipping carton is sealed with plastic tape and secured on the outside with plastic straps. The interior of the carton is fully lined with re-seal-able water-proof wrapping to protect the contents from external moisture; silica gel bags are also placed among the contents to absorb any condensation or moisture within the carton.

Before unpacking the unit:

• Inspect the carton for visible damage.

• Inspect the Drop and Tilt indicators (on the ShockWatch and TiltWatch labels, respectively) for evidence of accidental shock or tilting during transit (damage incident) - refer to Figure 3-1.

Chapter 3 - System Setup 3-5

PRELIMINARY

Tilt indicators turn Red

Drop indicators turn Red

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Figure 3-1 Drop and Tilt Indicators

NOTE: The above illustrations are examples only; indicators actually supplied may be different from those

above. If the carton is damaged, or if either the Drop or Tilt indicators have turned red (indicating damage

incident), please inform the GE sales representative immediately. In addition, mark on the shipping consignment note or packing slip/post-deliver y che cklist (in the “Package” column) that the Tilt and/or Drop indicators show damage incident.

3-6 Section 3-3 - Receiving and Unpacking the Equipment

Peripherals

Height

Width

FRONT

Depth

Ultrasound Scanner

Wooden Base

Note: Weight = 105 Kg (231 lbs)

Height

119 cm (47 in)

Width

73 cm (29 in)

FRONT

Depth

87 cm (34 in)

Note: Weight = 95 Kgs (209 lbs)

Plastic Straps

Adhesive Tape

Wooden Base

Note: Picture for illustration only

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

• Height, Width and Depth: See table below.

Figure 3-2 Shipping Carton size - Vivid™ S60/Vivid™ S70 with Peripherals

Figure 3-3 Shipping Carton - Vivid™ S60/Vivid™ S70 Scanner Only

Chapter 3 - System Setup 3-7

PRELIMINARY

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Table 3-3 Shipping Cartons - Dimensions and Weights

Description Height Width Depth

Vivid™ S60/Vivid™ S70 scanner with peripherals and accessories

Vivid™ S60/Vivid™ S70 scanner only

a. Weight is approximate and will vary depending upon the supplied peripherals

157 cm

62 in

119 cm

47 in

73 cm

29 in

73 cm

29 in

87 cm

34 in

87cm

34 in

Weight

105 kg

231 lbs

95 kg

209 lbs

3-8 Section 3-3 - Receiving and Unpacking the Equipment

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

3-3-3 Additional labels on the Shipping Carton

Figure 3-4 Additional Labels on Shipping Carton

Chapter 3 - System Setup 3-9

PRELIMINARY

CAUTION

Note: Picture for illustration only

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

3-3-4 Unpacking the Vivid™ S60/Vivid™ S70

As previously described, the Vivid™ S60/Vivid™ S70 ultrasound system is packe d in a single cardboard shipping carton comprising a durable outer cardboard carton cover and a wooden platform base ; these are firmly joined together with plastic straps. After completing a visual inspection of the shipping carton and Drop/Tilt indicators, proceed to the unpacking instructions below, as appropriate:

3-3-4-1 Unpacking the Vivid™ S60/Vivid™ S70 Scanner with Peripherals

1.) Cut the plastic straps securing the shipping carton to the wooden base - see Figure 3-2 on page 3-7.

WHEN USING SHARP TOOLS TO OPEN PACKING MATERIALS, TAKE CARE TO AVOID CUTTING OR DAMAGING ANY OF THE CONTENTS.

2.) Remove the options peripherals box (smaller-sized cardboard shippi ng ca rton ) fr om the top of the main cardboard shipping carton that contains the scanner.

3.) Carefully cut the adhesive tape used to close the shipping carton lids, and open the cartons from the top.

4.) Undo the re-seal-able water-proof carton liners.

5.) Remove the packing slip (shipping consignment note) detailing the conten ts of the shipping carton and keep close to hand ready to mark the check list - refer to Physical Inspection on page 3 - 21.

6.) Continue with unpacking the main cardboard shipping carton that contains the scanner, as indicated in Unpacking the Vivid™ S60/Vivid™ S70 Scanner on page 3 - 10.

3-3-4-2 Unpacking the Vivid™ S60/Vivid™ S70 Scanner

1.) Cut the two plastic straps securing the shipping carton to the wooden base.

WHEN USING SHARP TOOLS TO OPEN PACKING MATERIALS, TAKE CARE TO AVOID CUTTING OR DAMAGING ANY OF THE CONTENTS.

2.) Carefully cut the adhesive tape used to close the shipping carton upper lid and open the four folded flaps - see Figure 3-5.

Figure 3-5 Opening the Shipping Carton

3.) Remove the outer cardboard walls pulling them gently upwards and away from the system (Figure 3-6).

3-10 Section 3-3 - Receiving and Unpacking the Equipment

Wooden Base

Guide Rail

Wheeling Ramp

(in upright position)

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Figure 3-6 Wheeling Ramp in Upright Position

Note: The front side of the carton is reinforced with wooden guide rails and, when d ropped down

in the open position, these form a strong ramp used for wheeling the system out of the shipping carton.

4.) Remove the packing slip (shipping consignment note) detailing the conten ts of the shipping carton and keep close to hand ready to mark the check list - refer to Physical Inspection on page 3 - 21.

5.) From each side, remove the screws securing the scanner to the wooden base.

Chapter 3 - System Setup 3-11

PRELIMINARY

Foam Support

Wheeling Ramp

Foam Support

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

6.) Lower the wheeling ramp into the unloading position, as shown in Figure 3-7 on page 3-12.

Figure 3-7 Wheeling Ramp in Unloading Position for Scanner Removal

7.) Carefully remove the foam supports (from the side and top of the monitor) - see Figure 3-8.

Figure 3-8 Foam Supports Protecting the LCD Screen

3-12 Section 3-3 - Receiving and Unpacking the Equipment

CAUTION

NOTICE

Silica gel bags

Locking brake

Anti-static nylon on floor

Note: Picture for illustration only

(image does not show Touch Screen)

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

8.) Remove the two screws that secure the console holder, then remove the holder (Figure 3-7).

9.) Carefully remove the adhesive tape from the top of the system and spread the anti-static nylon on the floor.

10.)Remove any additional packing material from in front of and surrounding the system.

11.)Remove the two silica gel bags (Figure 3-9).

Figure 3-9 Locking Wheel Brake

12.)Press down on the locking brake to unlock the wheel. Repeat for the three other wheels.

13.)Using two people, carefully roll the scanner forwards down the unloading ramp to remove it completely from the shipping carton.

TWO PEOPLE ARE REQUIRED WHEN MOVING THE Vivid™ S60/Vivid™ S70 SCANNER.

This precaution is intended to prevent injury that may be caused by the weight of the system if one person attempts to move the scanner considerable distances or on an incline.

14.)Make sure the system is standing firmly on the floor before applying the locking brake.

15.)Remove the foam sections from the top of the system and from between the main shelf and probe shelf.

16.)Using the up/down handle, raise the main shelf up to appropriate height.

17.)Pull the monitor locking pin towards you and lift the monitor into the upr ight position.

18.)Before commencing the installation procedure, follow the instructions for Physical Inspection on

page 3 - 20.

After unpacking the unit: It is recommended to keep and store the shipping carton and all other packing materials (including the support foams, anti-st atic plast ic cover, et c.), in c ase the unit ha s to be mov ed to a different location in the future.

For warranty purposes, storage of the above is required for one year from date of purchase.

Chapter 3 - System Setup 3-13

PRELIMINARY

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

3-3-4-3 Unpacking the Ocean Shipping package

3-3-4-3-1 Part List

Table 3-4 Part List for Ocean shipping package

Item Description QTY Material

1 Pallet 1 Poplar plywood 2 Carton box 2 Corrugated card bo ard 3 Ex-Pak type-P lid 1 Poplar plywood 4 Foam for handle 1 PE, laminated 5 Foam for front 1 PE, laminated 6 Left foam 1 PE, laminated 7 Right foam 1 PE, laminated 8 Foam for plastic 1 PE, laminated

9 Tilt watch label 1

10 Anti-static nylon 1.5m 1 Nylon 11 Foam tube 4 PE, laminated 12 500g desiccant 2 Silica 13 Country specific label 1 Polyester 14 Chemical label for Alton system 1 Polyester 15 Ratchet tightening belt 1

Rigid polystyrene housing with

non-magnetic steel indicator

NOTE: The Item Numbers in the table above are referred where applicable in the procedure starting

on the next page.

3-14 Section 3-3 - Receiving and Unpacking the Equipment

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

3-3-4-4 Unpacking instruction (Ocean package)

Table 3-5 Unpacking instruction (Ocean package) 1 of 5

Chapter 3 - System Setup 3-15

PRELIMINARY

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Table 3-5 Unpacking instruction (Ocean package) (Continued) 2 of 5

3-16 Section 3-3 - Receiving and Unpacking the Equipment

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Table 3-5 Unpacking instruction (Ocean package) (Continued) 3 of 5

Chapter 3 - System Setup 3-17

PRELIMINARY

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Table 3-5 Unpacking instruction (Ocean package) (Continued) 4 of 5

3-18 Section 3-3 - Receiving and Unpacking the Equipment

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

Table 3-5 Unpacking instruction (Ocean package) (Continued) 5 of 5

Chapter 3 - System Setup 3-19

PRELIMINARY

WARNINGWARNING

IRECTION BC291740-1EN, REVISION 1 VIVID™ S60/VIVID™ S70 BASIC SERVICE MANUAL

3-3-5 Physical Inspection

Verify that the ultrasound system arrived intact (visual inspection). If the ultrasound system has been damaged, please refer to:

DAMAGE IN TRANSPORTATION on page - xiii in the beginning of this manual.

3-3-5-1 System Voltage Settings

Verify that the system voltage requirements meet the available voltage on site, refer Electrical

Requirements on page 2 - 3.

CONNECTING A VIVID™ S60/VIVID™ S70 SCANNER TO INCORRECT VOLTAGE LEVEL WILL MOST LIKELY DESTROY IT. CONNECT THE SYSTEM ONLY IN ACCORDANCE WITH THE VOLTAGE INDICATED ON THE PRODUCT LABEL.

3-3-6 EMI Protection

The Vivid™ S60/Vivid™ S70 ultrasound system 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.

3-20 Section 3-3 - Receiving and Unpacking the Equipment

General Electric Vivid S60 - Vivid S70 Basic Service Manual - v203_SM_BC291740-1EN_1 IMAGEWELL IMAGE CAPTURE KIT WITH SOFTWARE Owners Manual

Specifications and Main Features

Frequently Asked Questions

User Manual

Vivid™ S60/S70 Basic Service Manual

Important Precautions

TRANSLATION POLICY

DAMAGE IN TRANSPORTATION

CERTIFIED ELECTRICAL CONTRACTOR STATEMENT - FOR USA ONLY

OMISSIONS & ERRORS

SERVICE SAFETY CONSIDERATIONS

LEGAL NOTES

TRADEMARKS

COPYRIGHTS

Revision History

Section 1-1 Overview

1-1-1 Purpose of Chapter 1

1-1-2 Contents in this Chapter

Section 1-2 Service Manual Overview

1-2-1 Contents in this Service Manual

1-2-2 Typical Users of the Basic Service Manual

1-2-3 Vivid™ S60/Vivid™ S70 Models Covered in this Manual

1-2-4 Product Description

1-2-4-1 Overview of the Vivid™ S60/Vivid™ S70 Ultrasound Scanner

1-2-4-2 Purpose of Operator Manual(s)

Section 1-3 Important Conventions

1-3-1 Conventions Used in this Manual

1-3-1-1 Model Designations

1-3-1-2 Icons

1-3-1-3 Safety Precaution Messages

1-3-2 Standard Hazard Icons

Section 1-4 Safety Considerations

1-4-1 Introduction

1-4-2 Human Safety

1-4-3 Mechanical Safety

1-4-4 Electrical Safety

1-4-4-1 Probes

1-4-4-2 Peripherals

1-4-4-2-1 Safety and Environmental Guidelines

1-4-5 Vivid™ S60/Vivid™ S70 Battery Safety (part of Power Supply)

1-4-6 Patient Data Safety

Section 1-5 Dangerous Procedure Warnings

Section 1-6 Lockout/Tagout (LOTO) Requirements

Section 1-7 Product Labels and Icons

1-7-1 Universal Product Labels

1-7-1-1 System Rating Label

1-7-1-2 General Label

1-7-2 Label Descriptions

1-7-3 Vivid™ S60/Vivid™ S70 External Labels

1-7-3-1 GND Label

Section 1-8 Returning/Shipping Probes and Repair Parts

Section 1-9 EMC, EMI, and ESD

1-9-1 Electromagnetic Compatibility (EMC)

1-9-2 CE Compliance

1-9-3 Electrostatic Discharge (ESD) Prevention

1-9-4 General Caution

Section 1-10 Customer Assistance

1-10-1 Contact Information

1-10-1-1 Phone Numbers for Customer Assistance

1-10-1-2 Phone and Fax Numbers for Manufacturer

Section 2-1 Overview

2-1-1 Purpose of Chapter 2

Section 2-2 Console Requirements

2-2-1 Unit Environmental Requirements

2-2-1-1 Environmental Requirements - v203

2-2-2 Cooling Requirements

2-2-3 Lighting Requirements

2-2-4 Time and Manpower Requirements

2-2-5 Electrical Requirements

2-2-5-1 Vivid™ S60/Vivid™ S70 Power Requirements

2-2-5-3 Site Power Outlets

2-2-5-4 Mains Power Plug

Inrush Current

2-2-5-5 Power Stability Requirements

2-2-6 EMI Limitations

2-2-7 EMI Prevention/Abatement

2-2-8 Probe Environmental Requirements

Section 2-3 Facility Needs

2-3-1 Purchaser Responsibilities

2-3-3 Site Recommendations