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
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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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.
IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
Chapter 1
Introduction
Section 1-1
Overview
1-1-1Purpose 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.
IRECTION FR291740-1EN, REVISION 2VIVID 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.
1-2-1Contents 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 NUMBERTITLEDESCRIPTION
Chapter 1Introduction
Chapter 2Site Preparations
Chapter 3System Setup
Chapter 4
Chapter 5
Chapter 6Service Adjustments
Chapter 7Diagnostics/ Troubleshooting
Chapter 8Replacement Procedures
Chapter 9Renewal Parts
Chapter 10Care 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.
1-2Section 1-1 - Overview
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1-2-2Typical 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
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1-2-3Vivid™ S60N/Vivid™ S70N Models Covered in this Manual
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1-2-4Product Description
1-2-4-1Overview 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.
1-2-4-2Purpose 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
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Section 1-3
Important Conventions
1-3-1Conventions Used in this Manual
1-3-1-1Model 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.
1-3-1-2Icons
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.
1-3-1-3Safety 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.
1-6Section 1-1 - Overview
OR
TAG
&
EYE
PROTECTION
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1-3-2Standard 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
ELECTRICALMECHANICALRADIATION
LASERHEATPINCH
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 ELECTRICITYTAG AND LOCK OUTWEAR EYE PROTECTION
OR
HAND PROTECTIONFOOT PROTECTION
Chapter 1 - Introduction 1-7
PRELIMINARY
DANGER
WARNINGWARNING
WARNINGWARNING
WARNINGWARNING
WARNINGWARNING
WARNINGWARNING
WARNINGWARNING
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Section 1-4
Safety Considerations
1-4-1Introduction
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.
1-4-2Human 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.
1-8Section 1-1 - Overview
WARNINGWARNING
CAUTION
CAUTION
CAUTION
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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
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1-4-3Mechanical 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.
1-10Section 1-1 - Overview
CAUTION
CAUTION
CAUTION
CAUTION
CAUTION
CAUTION
WARNINGWARNING
CAUTION
WARNINGWARNING
WARNINGWARNING
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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.
Chapter 1 - Introduction 1-11
PRELIMINARY
WARNINGWARNING
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1-4-4Electrical 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 S70NSCANNER TO INCORRECT VOLTAGE LEVEL
WILL DESTROY THE SYSTEM!
CONNECT THE SYSTEM ONLY IN ACCORDANCE WITH THE VOLTAGE INDICATED ON
THE PRODUCT LABEL.
1-4-4-1Probes
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.
1-12Section 1-1 - Overview
WARNINGWARNING
WARNINGWARNING
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1-4-4-2Peripherals
1-4-4-2-1Safety and Environmental Guidelines
Environmental Dangers
All devices meeting IEC60950 must be kept outside the patient environment as defined
in IEC60601-1 Clause 16, unless the devices, according to IEC60601-1 Clause 16, are
equipped with the following:
A) Additional fixed earth protection
or:
B) An extra isolating transformer
Commercial devices such as laser cameras, printers, VCRs and external monitors,
usually exceed allowable leakage current limits and, when plugged into separate
AC outlets, are in violation of patient safety standards. Suitable electrical isolation of
such external AC outlets, or the provision of extra protective earth for the device, is
required in order to meet IEC60601-1 Clause 16 standards for electrical leakage.
•Patient Environment EN 60601-1
Sub clause 3.79 - Patient Environment
It is difficult for this standard to define dimensions for the volume in which diagnosis, monitoring or
treatment occurs. The dimensions for the PATIENT ENVIRONMENT given in Figure 1-1 have be en
justified in practice.
Figure 1-1 Example of Patient Environment
Chapter 1 - Introduction 1-13
PRELIMINARY
CAUTION
WARNINGWARNING
CAUTION
WARNINGWARNING
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1-4-5Vivid 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
1-4-6Patient 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.
1-14Section 1-1 - Overview
DANGER
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.
1-16Section 1-1 - Overview
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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.
1-7-1Universal 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.
1-7-1-1System 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 #DescriptionIllustration
1.
Rating Label - Vivid™ S60N/Vivid™ S70N
(100-240V)
(Assembled in China)
2.
Rating Label - Vivid™ S60N/Vivid™ S70N
(100-240V)
(Assembled in Romania)
Chapter 1 - Introduction 1-17
PRELIMINARY
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1-7-1-2General Label
A General Label (below) provides details regarding regulatory compliance - as well as warnings and
cautions.
Table 1-6 General Label - v203
Item #DescriptionIllustration
1.
General Label - International
(Manufactured in China)
2.
General Label - International
(Manufactured in Norway)
1-18Section 1-1 - Overview
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1-7-2Label 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 NamePurposeLocationStandard
Identification PlateManufacturer'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.
RearN/A- by GE Healthcare
Control panelIEC 60417-5010
Rear of system.
Probes.
IEC 60417-5333
Defibrillator-proof Type CF equipmentECG connectorIEC 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 currentVariousIEC 60417-5032
Protective earth (ground)InternalIEC 60417-5019
Rear of systemN/A- by certification body
Rear of system.IEC 60417-5140
Chapter 1 - Introduction 1-19
PRELIMINARY
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Table 1-7 Label Icons and Symbols - Description and Location (Continued)
Label NamePurposeLocationStandard
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 weightRear of systemN/A- by GE Healthcare
Rear of system.
Various.
Various.ISO 7010-W001
Rear of systemN/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
1-20Section 1-1 - Overview
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Table 1-7 Label Icons and Symbols - Description and Location (Continued)
Label NamePurposeLocationStandard
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 addressRear of system.ISO 7000-3082
Rear of system.ISO 7000-2497
Assembled in XXXXX
(XXXXX represents the
country name)
Serial number.
Brand and model identifierRear 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 identifierRear of systemN/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
Chapter 1 - Introduction 1-21
PRELIMINARY
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1-7-3Vivid 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.
1-7-3-1GND 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
1-22Section 1-1 - Overview
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IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
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.
Chapter 1 - Introduction 1-23
PRELIMINARY
WARNINGWARNING
WARNINGWARNING
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Section 1-9
EMC, EMI, and ESD
1-9-1Electromagnetic 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.
1-9-2CE 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.
1-24Section 1-8 - Returning/Shipping Probes and Repair Parts
WARNINGWARNING
WARNINGWARNING
CAUTION
WARNINGWARNING
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1-9-3Electrostatic 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.
1-9-4General 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.
Chapter 1 - Introduction 1-25
PRELIMINARY
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Section 1-10
Customer Assistance
1-10-1Contact 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
1-26Section 1-8 - Returning/Shipping Probes and Repair Parts
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1-10-1-1Phone Numbers for Customer Assistance
Table 1-8 Phone Numbers for Customer Assistance
Chapter 1 - Introduction 1-27
PRELIMINARY
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1-28Section 1-8 - Returning/Shipping Probes and Repair Parts
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Chapter 2
Site Preparations
Section 2-1
Overview
2-1-1Purpose 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.
IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
Section 2-2
Console Requirements
2-2-1Unit Environmental Requirements
2-2-1-1Environmental Requirements - v203
Table 2-1 Environmental Requirements - v 203
Relative Humidity
RequirementTemperature
(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.
2-2-2Cooling 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.
2-2-3Lighting 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.
2-2-4Time 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.
2-2Section 2-2 - Console Requirements
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2-2-5Electrical 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.
2-2-5-1Vivid S60N/Vivid S70N Power Requirements
Electrical specifications for the Vivid S60N/Vivid S70N system are as follows:
Table 2-2 Electrical Requirements
Input VoltageTolerancesOp. CurrentFrequency
100V AC to 240V AC±10%500VA50-60 Hz
2-2-5-2Inrush 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 V4.5 A
240 V2.3 A
2-2-5-3Site 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.
2-2-5-4Mains 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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2-2-5-5Power 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.
2-2-6EMI 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.
2-4Section 2-2 - Console Requirements
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2-2-7EMI Prevention/Abatement
The following table lists recommendations for preventing EMI:
Table 2-4 EMI Prevention/ Abatement
EMI RuleDetails
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.
2-2-8Probe 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
2-3-1Purchaser 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.
2-6Sect ion 2-3 - Facility Needs
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IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
2-3-2Mandatory 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.
2-3-3Site 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 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
2-3-3-1Recommended 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)
2-8Sect ion 2-3 - Facility Needs
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IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
2-3-3-2Minimal 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
1314
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IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
2-3-3-3Recommended 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
2-10Section 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 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
2-3-3-4Suggested 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 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
2-3-4Networking Pre-Installation Requirements
2-3-4-1Stand-alone Unit (without Network Connection)
None.
2-3-4-2Scanner Connected to Hospital’s Network
Supported networks:
•Wireless LAN
•10/100/1000 Mbps Ethernet/DICOM network
2-3-4-3InSite™ 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.
2-3-4-4Purpose 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.
2-3-4-5DICOM 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.
2-12Section 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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IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
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/REVISIONIP ADDRESSESPORTAE TITLE
Store 5
Store 6
Store 4
Storage
Commit
MPPS
Work list
...
...
...
...
...
...
...
...
...
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IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
Figure 2-6 Worksheet for DICOM Network Information
IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
Chapter 3
System Setup
Section 3-1
Overview
3-1-1Purpose 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.
IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
Section 3-2
Setup Reminders
3-2-1Average 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 minutesTime may vary, according to the required configuration
30 minutesTime 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.
3-2-2Setup 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.
3-2Section 3-2 - Setup Reminders
CAUTION
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IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
3-2-2-1System 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
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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IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
3-2-3Safety 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.
.
3-4Section 3-2 - Setup Reminders
CAUTION
CAUTION
CAUTION
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IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
Section 3-3
Receiving and Unpacking the Equipment
3-3-1Warnings 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.
3-3-2Overview
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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IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
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.
3-6Section 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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IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
Table 3-3 Shipping Cartons - Dimensions and Weights
DescriptionHeightWidthDepth
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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IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
3-3-3Additional labels on the Shipping Carton
Figure 3-3 Additional Labels on Shipping Carton
3-8Section 3-3 - Receiving and Unpacking the Equipment
CAUTION
CAUTION
Note: Picture for illustration only
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IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
3-3-4Unpacking 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:
3-3-4-1Unpacking 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.
3-3-4-2Unpacking 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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IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
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.
3-10Section 3-3 - Receiving and Unpacking the Equipment
Foam Support
Wheeling Ramp
Foam Support
Foam Support
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IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
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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IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
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.
3-12Section 3-3 - Receiving and Unpacking the Equipment
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IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
3-3-4-3Unpacking the Ocean Shipping package
3-3-4-3-1Part List
Table 3-4 Part List for Ocean shipping package
ItemDescriptionQTYMaterial
1Pallet1Poplar plywood
2Carton box2Corrugated card board
3Ex-Pak type-P lid1Poplar plywood
4Foam for handle1PE, laminated
5Foam for front1PE, laminated
6Left foam 1PE, laminated
7Right foam1PE, laminated
8Foam for plastic1PE, laminated
9Tilt watch label1
10Anti-static nylon 1.5m1Nylon
11Foam tube4PE, laminated
12500g desiccant2Silica
13Country specific label1Polyester
14Chemical label for Alton system1Polyester
15Ratchet tightening belt1
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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IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
3-3-4-4Unpacking instruction (Ocean package)
Table 3-5 Unpacking instruction (Ocean package) 1 of 5
3-14Section 3-3 - Receiving and Unpacking the Equipment
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IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
Table 3-5 Unpacking instruction (Ocean package) (Continued)2 of 5
Chapter 3 - System Setup 3-15
PRELIMINARY
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IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
Table 3-5 Unpacking instruction (Ocean package) (Continued)3 of 5
3-16Section 3-3 - Receiving and Unpacking the Equipment
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IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
Table 3-5 Unpacking instruction (Ocean package) (Continued)4 of 5
Chapter 3 - System Setup 3-17
PRELIMINARY
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IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
Table 3-5 Unpacking instruction (Ocean package) (Continued)5 of 5
3-18Section 3-3 - Receiving and Unpacking the Equipment
WARNINGWARNING
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IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
3-3-5Physical 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.
3-3-5-1System 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 S70NSCANNER TO INCORRECT VOLTAGE LEVEL
WILL MOST LIKELY DESTROY IT.
CONNECT THE SYSTEM ONLY IN ACCORDANCE WITH THE VOLTAGE INDICATED ON
THE PRODUCT LABEL.
3-3-6EMI 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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IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
Section 3-4
Preparing for Setup
3-4-1Verifying 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.
3-4-2Physical 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.
3-4-3Component 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.
3-4-3-1Damage 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
StepItemRecommended 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.
3-20Section 3-3 - Receiving and Unpacking the Equipment
Clamp securing AC cable
AC cable
AC cable secured with plastic clamp
D
IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
Probe HoldersClean the gel wells with warm water and a damp cloth to remove all traces of gel.
11
CoversCheck 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.
D
IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
3-4-3-2Front 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.
4Rear Handle16Up/down “Flex-Fit” Arm
5OPIO 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).
7Speakers: Two loudspeakers provided for Doppler sound.19Doppler 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.
12Front USB port.24
3-22Section 3-3 - Receiving and Unpacking the Equipment
13Front handle
14Probe-cable hooks
15Pull-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.
18Probe 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.
21Probe 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.
D
IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
3-4-3-3Rear View of the Vivid S60N/Vivid S70N ultrasound system
Figure 3-10 Vivid S60N/Vivid S70N Rear View
#Item#Item
1Display Monitor - rear9
2Touch Screen - rear10Power ON/OFF switch - provides power to the scanner
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).
11Ventilation port
12Black/White Video Printer (optional)
13CD/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
1234
5
6
D
IRECTION FR291740-1EN, REVISION 2VIVID S60N/VIVID S70N BASIC SERVICE MANUAL
3-4-3-4Peripheral/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
1Ethernet LAN connector — 1000 Base-TX Ethernet IEEE 802.3
2Isolated USB connector (USB 1.0 only)
3Dual USB connector
4DVI-D Display OUT connector (DVI-I type with digital output only [DVDI-D])
5LED - Network activity
6LED - Network activity
3-4-4EMI 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.
3-24Section 3-3 - Receiving and Unpacking the Equipment
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