General Electric Vivid S60N - Vivid S70N Basic Service Manual - v203_SM_FR291740-1EN_2 VIVID S60N AND VIVID S70N Basic Service Manual Software version v203 Direction Number: FR291740-1EN Revision: Rev. 2

PRELIMINARY
18.DEC.2018 VS60N-VS70N_FRNT_CVR.FM
g
Technical Publication
VIVID™ S60N AND VIVID™ S70N
Basic Service Manual
Software version v203
Direction Number: FR291740-1EN Revision: Rev. 2
BASIC SERVICE DOCUMENTATION. COPYRIGHT GENERAL ELECTRIC COMPANY.
© 2018 General Electric Company.
PRELIMINARY
18.DEC.2018 VS60N-VS70N_FRNT_CVR.FM
© 2018 General Electric Company.
Manufacturer:
GE Vingmed Ultrasound AS Strandpromenaden 45 3191 Horten NORWAY Tel: (+47) 3302 1100 Fax: (+47) 3302 1350
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Important Precautions

TRANSLATION POLICY

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DANGER
WARNINGWARNING
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DAMAGE IN TRANSPORTATION

All packages should be closely examined at time of delivery. If damage is apparent write “Damage In Shipment” on ALL copies of the freight or express bill BEFORE delivery is accepted or “signed for” by a GE representative or hospital receiving agent. Whether noted or concealed , damage MUST be reported to the carrier immediately upon discovery, or in any event, within 14 days after receipt, and the contents and containers held for inspection by the carrier. A transportation company will not pay a claim for damage if an inspection is not requested within this 14-day period.

CERTIFIED ELECTRICAL CONTRACTOR STATEMENT - FOR USA ONLY

All electrical Installations that are preliminary to positioning of the equipment at the site prepared for the equipment shall be performed by licensed electrical contractors. 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 any 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

© 2018 by General Electric Company Inc. All Rights Reserved.
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Revision History

Revision
1 2018-06-08 Initial version of manual. 2 2018-12-18 First released version of the manual.
Date
(YYYY-MM-DD)
Reason for change
List of Effected Pages (LOEP)
Pages Revision Pages Revision Pages Revision
Title Page 2 4-1 to 4-44 2 10-1 to 10-36 2
Important Precautions
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1-1 to 1-28 2 7-1 to 7-30 2 2-1 to 2-16 2 8-1 to 8-160 2 3-1 to 3-74 2 9-1 to 9-32 2
2 5-1 to 5-32 2 Back Cover N/A
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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™ S60N/Vivid™ S70N 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 S60N/Vivid S70N 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 - 19
Vivid S60N/Vivid S70N External Labels . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 22
Returning/Shipping Probes and Repair Parts. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1 - 23
EMC, EMI, and ESD. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 24
Electromagnetic Compatibility (EMC) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 24
CE Compliance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 24
Electrostatic Discharge (ESD) Prevention . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 25
General Caution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 25
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Customer Assistance. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 26
Contact Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 - 26
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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 - 8
Unpacking the Vivid S60N/Vivid S70N . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 9
Physical Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 19
EMI Protection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 19
Preparing for Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 20
Verifying Customer Order . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 20
Physical Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 20
Component Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 20
EMI Protection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 24
Completing the Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 25
Purpose of this Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 25
System Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 25
Electrical Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 27
Connections on the I/O Rear Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 27
Connections on the Patient I/O Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 28
Connecting Probes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 29
Power on/Boot up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 31
Power Shut Down . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 31
Complete Power Down . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 31
Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 32
Purpose of this Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 32
Ultrasound System Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 32
Service Screen Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 38
Optional Peripherals/Peripheral Connection . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 41
Software Options Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 43
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Connectivity Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 44
Physical Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 44
Stand-alone ultrasound system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 44
“Sneaker Net” Environment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 44
Wired Ethernet from ultrasound system to a Workstation . . . . . . . . . . . . . . . . 3 - 44
Connection from ultrasound system to a DICOM Server on a Network . . . . . . 3 - 44
Connectivity Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 45
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 45
Compatibility . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 45
Select TCP/IP Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 46
Changing the AE Title and/or Port Number (Port No.) . . . . . . . . . . . . . . . . . . . 3 - 47
Set the Remote Archive’s Network Information . . . . . . . . . . . . . . . . . . . . . . . . 3 - 47
Save the New Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 48
Wireless Network Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 49
Options Setup. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 50
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 50
Software Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 50
Color Video Printer Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 50
USB Flash Card Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 50
Tricefy™ . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 51
Wireless Network Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 52
Installation and set up of the View-X function . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 67
CARTO interface installation overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 68
Verifying/Installing SW option keys . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 71
External Monitor Output Resolution Adjustment . . . . . . . . . . . . . . . . . . . . . . . . 3 - 73
Paperwork After Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 74
Installation Acceptance Test Criteria . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 74
User’s Manual(s) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 74
Product Locator Installation Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 - 74
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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 S60N/Vivid S70N 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 S60N/Vivid S70N Ultrasound Scanner . . . 4 - 16
Cleaning the Trackball . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 18
Functional Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 19
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 19
Performance Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 19
2D Mode (B Mode) Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 20
M Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 23
Color Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 26
PW/CW Doppler Mode Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 31
Tissue Velocity Imaging (TVI) Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 34
Probe/Connectors Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 37
ECG Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 38
Cineloop Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 39
Back End Processor Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 40
Operating Panel Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 40
Main OLED/LCD Screen Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 41
External Monitor Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 41
Peripheral Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 41
Mechanical Functions Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 - 43
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IRECTION FR291740-1EN, REVISION 2 VIVID S60N/VIVID S70N 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™ S60N/Vivid™ S70N System Design. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5 - 4
User Interface Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 5
Main Scanner Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 5
Power Supply Section . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 - 5
Vivid™ S60N/Vivid™ S70N 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™ S60N/Vivid™ S70N Ultrasound Scanner - Electronic Cage (v203) . . . . . . . . . 5 - 11
Scanner Electronic Cage - Main Assemblies (v203) . . . . . . . . . . . . . . . . . . . . 5 - 11
Service Access to the Vivid S60N/Vivid S70N 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
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IRECTION FR291740-1EN, REVISION 2 VIVID S60N/VIVID S70N 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
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IRECTION FR291740-1EN, REVISION 2 VIVID S60N/VIVID S70N 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
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IRECTION FR291740-1EN, REVISION 2 VIVID S60N/VIVID S70N 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 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 9
Disruptive mode (v203) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 10
Color statuses . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 10
Licenses (v203) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7 - 11
Home (v203) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 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
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IRECTION FR291740-1EN, REVISION 2 VIVID S60N/VIVID S70N 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
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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 - 157
DVD/CD-RW Drive Replacement Procedure . . . . . . . . . . . . . . . . . . . . . . . . . 8 - 157
Black and White Printer Replacement Procedure . . . . . . . . . . . . . . . . . . . . . 8 - 159
-xii Table of Contents
PRELIMINARY
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IRECTION FR291740-1EN, REVISION 2 VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
CHAPTER 9 Renewal Parts
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 1
Purpose of Chapter 9 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 1
List of Abbreviations. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 3
Renewal Parts Lists and Diagrams . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9 - 4
Mechanical Hardware Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9 - 4
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
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IRECTION FR291740-1EN, REVISION 2 VIVID S60N/VIVID S70N 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
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IRECTION FR291740-1EN, REVISION 2 VIVID S60N/VIVID S70N 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™ S60N/Vivid™ S70N 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. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-23
1-9 EMC, EMI, and ESD. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-24
1-10 Customer Assistance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-26
Chapter 1 - Introduction 1-1
PRELIMINARY
D
IRECTION FR291740-1EN, REVISION 2 VIVID S60N/VIVID S70N BASIC SERVICE MANUAL

Section 1-2 Service Manual Overview

This manual provides setup and service information for the Vivid™ S60N/Vivid™ S70N ultrasound
scanner. The ten chapters it contains are outlined in Table 1-1 below.

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™ S60N/Vivid™ S70N
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 the Vivid™ S60N/Vivid™ S70N ultrasound scanner.
Provides instructions for setting up and running diagnostic, troubleshooting and other related routines for the Vivid™ S60N/ Vivid™ S70N 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™ S60N/Vivid™ S70N ultrasound scanner.
Provides periodic maintenance procedures for the Vivid™ S60N/ Vivid™ S70N 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
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IRECTION FR291740-1EN, REVISION 2 VIVID S60N/VIVID S70N 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
D
IRECTION FR291740-1EN, REVISION 2 VIVID S60N/VIVID S70N BASIC SERVICE MANUAL

1-2-3 Vivid™ S60N/Vivid™ S70N Models Covered in this Manual

Table 1-2 Vivid™ S60N/Vivid™ S70N Models
Product Cat No. Part Number Description
Vivid S70N v203CH H45601GA BC000700 Vivid™ S70N ultrasound imaging scanner Vivid S70N v203 H45601GC FR000700 Vivid™ S70N ultrasound imaging scanner Vivid S70N v203 Russia H45601RZ FR000700-RU Vivid™ S70N ultrasound imaging scanner Vivid S60N v203CH H45601GB BC000710 Vivid™ S60N ultrasound imaging scanner Vivid S60N v203 H45601GD FR000710 Vivid™ S60N ultrasound imaging scanner Vivid S60N v203 Russia H45601SA FR000710-RU Vivid™ S60N ultrasound imaging scanner
1-4 Section 1-1 - Overview
D
IRECTION FR291740-1EN, REVISION 2 VIVID S60N/VIVID S70N BASIC SERVICE MANUAL

1-2-4 Product Description

1-2-4-1 Overview of the Vivid S60N/Vivid S70N Ultrasound Scanner
The Vivid S60N/Vivid S70N 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 S60N/Vivid S70N 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 S60N/Vivid S70N. 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 S60N/Vivid S70N system, and also kept near the unit for quick reference.
Chapter 1 - Introduction 1-5
PRELIMINARY
DANGER
WARNINGWARNING
CAUTION
D
IRECTION FR291740-1EN, REVISION 2 VIVID S60N/VIVID S70N 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 S60N/Vivid S70N ultrasound units listed in Vivid™ S60N/Vivid™ S70N
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
OR
TAG
&
EYE
PROTECTION
D
IRECTION FR291740-1EN, REVISION 2 VIVID S60N/VIVID S70N 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 S60N/Vivid S70N system has no uninte nded 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 a rm).
Table 1-4 Standard Icons Indicating a Special Procedure Be Used
AVOID STATIC ELECTRICITY TAG AND LOCK OUT WEAR EYE PROTECTION
OR
HAND PROTECTION FOOT PROTECTION
Chapter 1 - Introduction 1-7
PRELIMINARY
DANGER
WARNINGWARNING
WARNINGWARNING
WARNINGWARNING
WARNINGWARNING
WARNINGWARNING
WARNINGWARNING
D
IRECTION FR291740-1EN, REVISION 2 VIVID S60N/VIVID S70N 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 o ve the Ultrasound system covers.
Servicing should be performed by authorized personnel only.
Only personnel who have participated in a Vivid S60N/Vivid S70N Trainin g 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 S60N/VIVID S70N 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 S60N/VIVID S70N 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
CAUTION
CAUTION
D
IRECTION FR291740-1EN, REVISION 2 VIVID S60N/VIVID S70N 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
WARNINGWARNING
DANGER
DANGER
DANGER
CAUTION
WARNINGWARNING
WARNINGWARNING
D
IRECTION FR291740-1EN, REVISION 2 VIVID S60N/VIVID S70N 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™ S60N/VIVID™ S70N 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™ S60N/Vivid™ S70N ultrasound scanner weighs 75kg (165 lb s.) or 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 S60N/Vivid S70N 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.
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CAUTION
CAUTION
CAUTION
CAUTION
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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.
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.
-
ALWAYS:
DO NOT TRANSPORT THE VIVID S60N/VIVID S70N 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 S60N/VIVID S70N 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 S60N/Vivid S70N 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 S60N/Vivid S70N 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.
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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 international electrical standards.
CONNECTING A VIVID S60N/VIVID S70N 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 S60N/Vivid S70N 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 ™ S60N/Vivid™ S70N User Manual for detailed probe handling instructions.
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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
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1-4-5 Vivid S60N/Vivid S70N Battery Safety (part of Power Supply)

NOTE: The Vivid™ S60N/Vivid™ S70N ultrasound scanner is supplied with a lithium 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 S60N/VIVID S70N ULTRASOUND SCANNER
The Vivid S60N/Vivid S70N 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.
o
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
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WARNINGWARNING
WARNINGWARNING
DANGER
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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 S60N/VIVID S70N 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
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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™ S60N/VIVID™ S70N. 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.
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Section 1-7 Product Labels and Icons

The Vivid™ S60N/Vivid™ S70N 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 S60N/Vivid S70N ultrasound unit. For an
explanation of label icons and symbols, refer to Table 1-7 on page 1-19.
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 - v203
Item # Description Illustration
1.
Rating Label - Vivid™ S60N/Vivid™ S70N
(100-240V)
(Assembled in China)
2.
Rating Label - Vivid™ S60N/Vivid™ S70N
(100-240V)
(Assembled in Romania)
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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 - v203
Item # Description Illustration
1.
General Label - International
(Manufactured in China)
2.
General Label - International
(Manufactured in Norway)
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1-7-2 Label Descriptions

The following table shows the labels and symbols that may be found on the Vivid S60N/Vivid S70N 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
Identification Plate Manufacturer's name and address
Model Device Listing/Certification Labels
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 N/A- by GE Healthcare
Control panel IEC 60417-5010
Rear of system. Probes.
IEC 60417-5333
Defibrillator-proof Type CF equipment ECG connector IEC 60417-5336
Indicates that the product is in compliance with all relevant European Directives and under surveillance by Notified Body 0123.
Non-ionizing electromagnetic radiation.
Alternating current Various IEC 60417-5032
Protective earth (ground) Internal IEC 60417-5019
Rear of system N/A- by certification body
Rear of system. IEC 60417-5140
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Table 1-7 Label Icons and Symbols - Description and Location (Continued)
Label Name Purpose Location Standard
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.
Attention - Consult accompanying documents: Alerts the user to refer to the user documentation when complete information cannot be provided on the label.
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. Various.
Various. ISO 7010-W001
Rear of system N/A- by GE Healthcare
Top console (both sides).
Display rear panel.
Rear of system. EN 50419
ISO 7010-W012
ISO 7010-P017
ISO 7010-P012
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Table 1-7 Label Icons and Symbols - Description and Location (Continued)
Label Name Purpose Location Standard
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
Rear of system. ISO 7000-2497
Assembled in XXXXX (XXXXX represents the country name)
Serial number.
Brand and model identifier Rear of system. ISO 7000-3082
Unique Device Identification (UDI). Every system has a unique marking for identification. Scan or enter the UDI information into the patient health record as required by governing laws.
Device part number identifier Rear of system N/A- by GE Healthcare
Identify the Customs Country of Origin of the materials.
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.
Rear of the system.
Rear of system. N/A- by GE Healthcare
Rear of system. N/A- by GE Healthcare
Service documentation
ISO 7000-2498
N/A- by GE Healthcare
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1-7-3 Vivid S60N/Vivid S70N External Labels

In addition to the labels described in the previous section, an additional label may be found on the Vivid S60N/Vivid S70N ultrasound system, as described in the following section.
1-7-3-1 GND Label
Indicates the protective earth (grou ndin g) ter mina l. The GND la bel ( F igur e 1-2 below) is located at the rear of the system.
Figure 1-2 GND Label
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Section 1-8 Returning/Shipping Probes and Repair Parts

Equipment being returned must be clean and free of blood and other infectious substances. GE policy states that body fluids must be properly removed from any part or equipment prior to
shipment. GE employees, as well as customers, are responsible for ensuring 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, bod y 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 “regulate d medi cal waste” for transportation pur poses 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™ S60N/Vivid™ S70N ultrasound scanner is not meant to be used for long-term storage of patient data or images. The user is responsible for the data on the Vivid S60N/Vivid S70N and a regular backup is highly recommended.
If the Vivid S60N/Vivid S70N is sent for repair, ensure that any patient information is backed up and erased from the Vivid S60N/Vivid S70N before shipping. It is always possible during system failure and repair to lose patient data. GE is not responsible for the loss of this data.
If PHI (Patient Healthcare Information) data needs to be sent to GE employees for service purposes, GE will ascertain agreement from the customer. Patient information shall only be transferred by approved service processes, tools and devices restricting access, protecting or encrypting data 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.
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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 referred to as radio–frequency or electromagnetic interference (RFI/EMI) and can be radiated throu gh space or conducted over interconnecting power or signal cables. In addition to electromagnetic ener gy, EMC also includes possible effects from electrical fields, magnetic fields, electrostatic discharge and disturbances in the electrical power supply.
NOTE: The Vivid™ S60N/Vivid™ S70N ultrasound scanner needs special precautions regarding EMC and
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™ S60N/Vivid™ S70N
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™ S60N/VIVID™ S70N AS REPLACEMENT PARTS FOR INTERNAL COMPONENTS, MAY RESULT IN INCREASED EMISSIONS OR DECREASED IMMUNITY OF THE VIVID™ S60N/VIVID™ S70N.
THE VIVID™ S60N/VIVID™ S70N SHOULD NOT BE USED ADJACENT TO OR STACKED WITH OTHER EQUIPMENT AND THAT IF ADJACENT OR STACKED USE IS NECESSARY, THE VIVID™ S60N/VIVID™ S70N SHOULD BE OBSERVED TO VERIFY NORMAL OPERATION IN THE CONFIGURATION IN WHICH IT WILL BE USED.

1-9-2 CE Compliance

The Vivid™ S60N/Vivid™ S70N ultrasound scanner conform s 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™ S60N/Vivid™ S70N User Manual. NOTE: For EMC Guidance and Manufacturer’s Declarations, refer to the tables provided in Electrostatic
Discharge (ESD) Prevention on page 1 - 25.
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.
1-24 Section 1-8 - Returning/Shipping Probes and Repair Parts
WARNINGWARNING
WARNINGWARNING
CAUTION
WARNINGWARNING
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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 appr oved by the manufacturer. Ignoring this advice may compromise the regulatory approvals obtained for the product.
IF THE COVERS ARE REMOVED FROM AN OPERATING VIVID™ S60N/VIVID™ S70N, SOME METAL SURFACES MAY BE WARM ENOUGH TO POSE A POTENTIAL HEAT HAZARD IF TOUCHED, EVEN WHILE IN SHUTDOWN MODE.
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Section 1-10 Customer Assistance

1-10-1 Contact Information

If this equipment does not operate as indicated in this Service Manual or in the Vivid™ S60N/Vivid™ S70N 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 ca ll:
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.
See also:
Phone Numbers for Customer Assistance on page 1 - 27
Phone and Fax Numbers for Manufacturer on page 1 - 28
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1-10-1-1 Phone Numbers for Customer Assistance
Table 1-8 Phone Numbers for Customer Assistance
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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 VINGMED ULTRASOUND A/S STRANDPROMENADEN 45 P.O. BOX 141 3191 HORTEN NORWAY
This page was intentionally left blank.
+47 3302 1100 +47 3302 1350
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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™ S60N or Vivid™ S70N ultrasound system. Included are descriptions of the electrical and facility requirements 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
CAUTION
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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
-20 — +60
o
C (50 — 95oF)
o
C (-4 — 140oF)
o
C (-4 — 140oF))
30 — 85% 700 — 1060 hPa
10 — 95% 700 — 1060 hPa
10 — 95% 700— 1060 hPa
NOTE: The Vivid S60N/Vivid S70N system may be ope rat ed 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 S60N/Vivid S70N 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 S60N/Vivid S70N 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
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IRECTION FR291740-1EN, REVISION 2 VIVID S60N/VIVID S70N 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 S60N/Vivid S70N Power Requirements
Electrical specifications for the Vivid S60N/Vivid S70N 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 S60N/Vivid S70N 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
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IRECTION FR291740-1EN, REVISION 2 VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
2-2-5-5 Power Stability Requirements
Voltage drop-out
Max 10 msec
Power Transients
The Vivid™ S60N/Vivid™ S70N 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 S60N/Vivid S70N 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
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IRECTION FR291740-1EN, REVISION 2 VIVID S60N/VIVID S70N 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
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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 to 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
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IRECTION FR291740-1EN, REVISION 2 VIVID S60N/VIVID S70N 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 Recomme ndations (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
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IRECTION FR291740-1EN, REVISION 2 VIVID S60N/VIVID S70N 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
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IRECTION FR291740-1EN, REVISION 2 VIVID S60N/VIVID S70N 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
4
1
2
18
5
6
9
16
17
15
8
7
10
11
12
3
13 14
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IRECTION FR291740-1EN, REVISION 2 VIVID S60N/VIVID S70N 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)
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IRECTION FR291740-1EN, REVISION 2 VIVID S60N/VIVID S70N 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
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IRECTION FR291740-1EN, REVISION 2 VIVID S60N/VIVID S70N 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 S60N/Vivid S70N ultrasound system to work with other network conn ections, the network administrator must provide the required information, which should include the following:
Details: DICOM network details for the Vivid S60N/Vivid S70N unit, including the host name, local port, IP address, AE title and net mask.
Routing Information: IP addresses for the default gateway 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 S60N/ Vivid S70N 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:
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Section 2-4 Connectivity Installation Worksheet

Figure 2-5 Connectivity Installation Worksheet
Chapter 2 - Site Preparations 2-13
PRELIMINARY
Vivid S60N/Vivid S70N 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
...
...
...
...
...
...
...
...
...
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IRECTION FR291740-1EN, REVISION 2 VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
Figure 2-6 Worksheet for DICOM Network Information
2-14 Section 2-4 - Connectivity Installation Worksheet
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Table 2-6 Vivid S60N/Vivid S70N 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
D
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This page was intentionally left blank.
2-16 Section 2-4 - Connectivity Installation Worksheet
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IRECTION FR291740-1EN, REVISION 2 VIVID S60N/VIVID S70N 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 S60N/Vivid S70N 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 tha t 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. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-20
3-5 Completing the Setup. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-25
3-6 Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-32
3-7 Connectivity Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-44
3-8 Connectivity Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-45
3-9 Options Setup. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-50
3-10 Paperwork After Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-74
Chapter 3 - System Setup 3-1
PRELIMINARY
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Section 3-2 Setup Reminders

3-2-1 Average Setup Time

The Vivid S60N/Vivid S70N setup and functional checkout will take approximately one hour; Vivid S60N/Vivid S70N consoles with optional equipment (such as Alphanumeric Keyboard) may take slightly 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 S60N/Vivid S70N 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 3-3 on
page 3-8.
3-2 Section 3-2 - Setup Reminders
CAUTION
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3-2-2-1 System Acclimation Time
Following transport, the Vivid S60N/Vivid S70N 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
o
C or above 40oC.
o
C increment,
Turning the system ON after arrival at the site - without allowing time for acclimation - may cause system damage!
Table 3-2 Vivid S60N/Vivid S70N 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
CAUTION
CAUTION
CAUTION
WARNINGWARNING
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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 S60N/Vivid S70N 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™ S60N/Vivid™ S70N 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
CAUTION
CAUTION
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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 S60N/Vivid S70N 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 S60N/Vivid S70N 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 S60N/Vivid S70N Scanner with Peripherals on page 3 - 9
Unpacking the Vivid S60N/Vivid S70N Scanner on page 3 - 9
Unpacking the Ocean Shipping package on page 3 - 13
NOTE: For details of weights and dimensions of the shipping cartons, refer to Table 3-3 on page 3- 7.
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:
Ins pe ct the ca rto n for visib le da m ag e .
Inspect the Tilt indicators (on the TiltWatch labels) 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
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Figure 3-1 Drop and Tilt Indicators
NOTE: The above illustrations are examples only; indicators actually supplied may be differ from those above.
If the carton is damaged, or if the Tilt indicators have turned red (indicating damage incident), please inform the GE sales repr esentative immediately. In addition, mark on the shipp ing consignment note or packing slip/post-delivery checklist (in the “Package” column) that the Tilt 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)
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Height, Width and Depth: Se table below.
Figure 3-2 Shipping Carton size - Vivid S60N/Vivid S70N with Peripherals
Table 3-3 Shipping Cartons - Dimensions and Weights
Description Height Width Depth
Vivid S60N/Vivid S70N scanner
with peripherals and accessories
Vivid S60N/Vivid S70N 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
a
Chapter 3 - System Setup 3-7
PRELIMINARY
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3-3-3 Additional labels on the Shipping Carton

Figure 3-3 Additional Labels on Shipping Carton
3-8 Section 3-3 - Receiving and Unpacking the Equipment
CAUTION
CAUTION
Note: Picture for illustration only
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3-3-4 Unpacking the Vivid S60N/Vivid S70N

As previously described, the Vivid S60N/Vivid S70N ultrasound system is packed in a single cardboard shipping carton comprising a durable outer cardboard carton cover and a wooden platform ba se; these are firmly joined together with plastic straps. After completing a visual inspection of the shippin g carton and Drop/Tilt indicators, proceed to the unpacking instructions below, as appropriate:
3-3-4-1 Unpacking the Vivid S60N/Vivid S70N 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 shipp ing ca rton ) fr om th e 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 - 20.
6.) Continue with unpacking the main cardboard shipping carton th at contains the scanner, as indicated in Unpacking the Vivid S60N/Vivid S70N Scanner on page 3 - 9.
3-3-4-2 Unpacking the Vivid S60N/Vivid S70N 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 op en the four folded flaps - see Figure 3-4.
Figure 3-4 Opening the Shipping Carton
3.) Remove the outer cardboard walls pulling them gently upwards and away from the system (Figure 3-5).
Chapter 3 - System Setup 3-9
PRELIMINARY
Wooden Base
Guide Rail
Wheeling Ramp
(in upright position)
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Figure 3-5 Wheeling Ramp in Upright Position
Note: The front side of the carton is reinforced with wooden guide rails and, when dropped 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 - 20.
5.) From each side, remove the screws securing the scanner to the wooden base.
3-10 Section 3-3 - Receiving and Unpacking the Equipment
Foam Support
Wheeling Ramp
Foam Support
Foam Support
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6.) Lower the wheeling ramp into the unloading position, as shown in Figure 3-6 on page 3-11.
Figure 3-6 Wheeling Ramp in Unloading Position for Scanner Removal
7.) Carefully remove the foam supports (from the side and top of the monitor) - see Figure 3-7.
Figure 3-7 Foam Supports Protecting the LCD Screen
Chapter 3 - System Setup 3-11
PRELIMINARY
CAUTION
NOTICE
Silica gel bags
Locking brake
Anti-static nylon on floor
Note: Picture for illustration only
(image does not show Touch Screen)
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8.) Remove the two screws that secure the console holder, then remove the holder (Figure 3-6).
9.) Carefully remove the adhesive tape from the top of th e syste m and spread the anti-static nylo n 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 3-8).
Figure 3-8 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 S60N/Vivid S70N 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 upright position.
18.)Before commencing the installation procedure, follow the instructions for Physical Inspection on
page 3 - 19.
After unpacking the unit: It is recommended to keep and store the shipping carton and all other packing materials (including the support foams, anti-static plastic 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.
3-12 Section 3-3 - Receiving and Unpacking the Equipment
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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 board 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.
Chapter 3 - System Setup 3-13
PRELIMINARY
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3-3-4-4 Unpacking instruction (Ocean package)
Table 3-5 Unpacking instruction (Ocean package) 1 of 5
3-14 Section 3-3 - Receiving and Unpacking the Equipment
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Table 3-5 Unpacking instruction (Ocean package) (Continued)2 of 5
Chapter 3 - System Setup 3-15
PRELIMINARY
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Table 3-5 Unpacking instruction (Ocean package) (Continued)3 of 5
3-16 Section 3-3 - Receiving and Unpacking the Equipment
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Table 3-5 Unpacking instruction (Ocean package) (Continued)4 of 5
Chapter 3 - System Setup 3-17
PRELIMINARY
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Table 3-5 Unpacking instruction (Ocean package) (Continued)5 of 5
3-18 Section 3-3 - Receiving and Unpacking the Equipment
WARNINGWARNING
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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 S60N/VIVID S70N 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 S60N/Vivid S70N 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.
Chapter 3 - System Setup 3-19
PRELIMINARY
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Section 3-4 Preparing for Setup

3-4-1 Verifying Customer Order

Compare items received by the customer to that which is listed on the delivery or der. Report any items that are missing, back ordered, or damaged.

3-4-2 Physical Inspection

Verify that the ultrasound system arrived intact (visual inspection). If the ultrasound system has been damaged, please refer to DAMAGE IN TRANSPORT ATION on page
xiii in the beginning of this manual.

3-4-3 Component Inspection

After verifying that all the required parts are included in the shipping crate, inspect the system components using the checklist supplied below. In addition, ensure that all the labels described in Chapter 1 -
Introduction are present, accurate and in good condition, and enter the serial number printed on the main
label into the system installation details card, as described in Paperwork After Setup on page 3-74.
3-4-3-1 Damage Inspection Checklist
Visually inspect the contents of the shipping carton for damage. If any parts are damaged or missing, contact an authorized GE Service Representative.
A Damage Inspection Checklist for the Vivid S6 0N/Vivid S70N portable ultrasound scan ner is provided in Table 3-6 below.
Table 3-6 Damage Inspection Checklist - Vivid S60N/Vivid S70N Systems
Step Item Recommended Procedure
1
Console
2
Control Console
3
Probes
4
LCD Display
5
Touch Screen
6
Fans
Verify that the system is switched OFF and unplugged. Clean the console and control panel.
Physically inspect the control console for missing or damaged items. Verify the proper illumination of all the control panel buttons.
Check all probes for wear and tear on the lens, cable, and connector. Look for bent or damaged pins on the connector and in the connector socket on the unit. Verify that the EMI fingers around the probe connector socket housing are intact. Check the probe locking mechanism and probe switch.
Clean the LCD display by gently wiping with a dry, soft, lint-free non-abrasive folded cloth. Inspect the monitor for scratches and raster burn.
Clean the Touch Screen by gently wiping with a dry, soft, lint-free non-abrasive folded cloth. Inspect the screen surface for scratches and raster burn.
Turn on the system and verify that the system’s cooling fans and peripheral fans are operating.
7
8
9
Rear Panel
Covers
Peripherals
Check the rear panel connectors for bent pins, loose connections and loose or missing hardware. Screw all the cable connectors tightly to the connector sockets on the panel. Verify that the labeling is in good condition.
Check that all screws are tightly secured in place, that there are no dents or scratches and that no internal parts are exposed.
Check and clean the peripherals in accordance with the manufacturer’s directions. To prevent EMI or system overheating, dress the peripheral cables inside the peripheral cover.
3-20 Section 3-3 - Receiving and Unpacking the Equipment
Clamp securing AC cable
AC cable
AC cable secured with plastic clamp
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Table 3-6 Damage Inspection Checklist - Vivid S60N/Vivid S70N Systems (Continued)
Step Item Recommended Procedure
10
Probe Holders Clean the gel wells with warm water and a damp cloth to remove all traces of gel.
11
Covers Check that all screws are in place, all chassis and internal covers are installed.
12
13
14
Peripherals
AC System
Power Cord
Check and clean the peripherals in accordance with the manufacturer’s directions. To prevent EMI or system overheating, dress the peripheral cables inside the peripheral cover.
Check the AC board connectors and the associated cabling for good connection and proper insulation. Verify that the connections are secured.
Check the power cord for cuts, loose hardware, tire marks, exposed insulation, or any deterioration. Verify continuity.
Tighten the clamps that secure the power cord to the unit and the outlet plug to the cord. Replace the power cord and/or clamp, as required.
Note! Illustration is for a v201 system.
Secure the cable to the back of the system using the plastic clamp provided.
15
Plastic Clamp
16
Front Casters
17
Rear Casters
Chapter 3 - System Setup 3-21
Note! Illustration is for a v201 system.
Check that the front casters can roll and swivel, and can be placed in the locked position by pressing the foot brake (lower lever) down on each. Ensure that the wheels are locked and there is no movement in any direction.
Check that the front casters can roll and swivel, and can be placed in the locked position by pressing the foot brake (lower lever) down on each. Ensure that the wheels are locked, unable to swivel left or right, and that there is no movement forwards or backwards.
PRELIMINARY
1
2
3
10 11
23
17
24
9
4
8
5
6
15
13
7
22
16
18
21
19
20
12 14
Note! Illustration is for a v201 system.
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3-4-3-2 Front View of the Vivid S60N/Vivid S70N ultrasound system
Figure 3-9 Front View of the Vivid S60N/Vivid S70N Ultrasound Scanner
# Item # Item
Display Monitor:
1
Tilts up and down and swivels left and right. Touch Screen: Mounted in a fixed position behind the Control
2
Panel at a convenient angle for viewing. Monitor Articulated Arm. Includes Release pin that enables
3
locking of the monitor in the 90 degree position.
4 Rear Handle 16 Up/down “Flex-Fit” Arm 5 OPIO Basket: Holds paper and other utensils, as required. 17
ON/OFF: Power ON/OFF knob enables the user turn ON the
6
system (when power is connected and the system is either in Shutdown or Standby mode).
7 Speakers: Two loudspeakers provided for Doppler sound. 19 Doppler Pencil Probe Connector
Control Panel: Contains the buttons used to operate the
8
ultrasound system and the alphanumeric keyboard (optional).
Probe and gel holders: Provides a safe, rubber-cushioned
9
resting place for probes. (Both sides of the Control Panel). Control Panel swivel release handle: Enables locking of the
10
control panel in position; swiveling it left or right. Control Panel up/down release handle:
Enables locking of the control panel in position, or changing
11
the location of the arm by moving it upwards and away from the user, or downwards and away from the system. Provides leg room for the user who may then be seated beside system.
12 Front USB port. 24
3-22 Section 3-3 - Receiving and Unpacking the Equipment
13 Front handle
14 Probe-cable hooks
15 Pull-out Alphanumeric Keyboard (optional)
Air inlet and Sub-woofer: Air flow is via a built-in filter on the side cover, for system air cooling. A sub woofer speaker provides superb sound.
18 Probe Connectors (PDT type)
ECG Cable Connector: Provides External ECG input connection to an ECG monitor device outlet, or direct patient three-contact ECG lead
20
connection. Important: Do not use the Vivid 7 ECG cable with the Vivid S60N/Vivid S70N system.
21 Probe Connector (RS type for TEE probe).
Rear Caster Wheel: Enables locking of swivel motion, or free rolling and
22
swiveling.
Probe-cable management tray (removable). Note: should be used only
23
for small-footprint items of a total weight not exceeding 1 Kg (2.2 lbs).
Front Caster Wheel: Enables full-locking of swivel motion, or free rolling and swiveling.
1
2
4
3
6
5
7
8
9
10
11
12
13
16
15
14
Note! Illustration is for a v201 system.
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3-4-3-3 Rear View of the Vivid S60N/Vivid S70N ultrasound system
Figure 3-10 Vivid S60N/Vivid S70N Rear View
# Item # Item
1 Display Monitor - rear 9
2 Touch Screen - rear 10 Power ON/OFF switch - provides power to the scanner
3
4
5
6 System Labels 14
7 Rear Wheels - Swivel 15 Doppler Speakers 8 Ground - detachable Ground plug. 16 Articulated Arm
Gel Holders: Provides convenient storage for US Gel bottles. Holders are situated on either side of the control console.
Rear Handle: used to pull/push the scanner and place it in the desired position.
Rear I/O Peripheral/Accessory Connector Panel: Provides ports for LAN, Insulated USB, Dual USB and DVI, (see Figure 3-11).
11 Ventilation port
12 Black/White Video Printer (optional)
13 CD/DVD Drive
Main power input socket (AC IN); fitted with a safety spring for securing AC power cable.
Rear Cable Hooks: provides a cable management solution for probes and ECG leads.
Chapter 3 - System Setup 3-23
PRELIMINARY
1 2 3 4
5 6
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3-4-3-4 Peripheral/Accessory Connector Panel
Figure 3-1 1 shows a view of the Vivid S60N/Vivid S70N ultrasound system rear panel showing external
peripheral/accessory connectors.
Figure 3-11 View of the Vivid S60N/Vivid S70N Peripheral/Accessory Connector Panel
1 Ethernet LAN connector — 1000 Base-TX Ethernet IEEE 802.3 2 Isolated USB connector (USB 1.0 only) 3 Dual USB connector 4 DVI-D Display OUT connector (DVI-I type with digital output only [DVDI-D]) 5 LED - Network activity 6 LED - Network activity

3-4-4 EMI Protection

The 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 ultrasound 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 ultrasound system is put into operation.
See EMI Limitations on page 2 - 4 for more information about EMI protection.
3-24 Section 3-3 - Receiving and Unpacking the Equipment
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