GE Vivid 7 User Manual

Safety
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infection. Inspect probes frequently for sharp, pointed or rough 
surface damage that could cause injury or tear protective 
barriers (gloves and sheaths).
Transesophageal probe safety 
Never use excessive force when manipulating the 
transesophageal probe. The detailed operator manual 
enclosed with the transesophageal probe must be read 
carefully.
Electrical Hazard 
A damaged probe may increase the risk of electric shock if 
conductive solutions...

Safety
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Personnel and equipment safety
Explosion hazard
Never operate the equipment in the presence of flammable or 
explosive liquids, vapors or gases. Malfunctions in the unit, or 
sparks generated by fan motors, can electrically ignite these 
substances. Operators should be aware of the following points 
to prevent such explosion hazards.
•  If flammable substances are detected in the environment, 
do not plug in or turn on the system. 
•  If flammable...

Safety
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seeping into the active circuit components may cause short 
circuiting, which could result in an electrical fire. 
•  An electrical hazard may exist if any light, monitor or visual 
indicator remains on after the unit is turned off.
Fuses blown within 36 hours of being replaced may indicate a 
malfunctioning electrical circuit within the system. In this event, 
the unit must be checked by GE Ultrasound service personnel. 
No attempt should be made to...

Safety
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Pacemaker hazard
The possibility of the system interfering with pacemakers is 
minimal. However, as this system generates high frequency 
electrical signals, the operator should be aware of the potential 
hazard this could cause. 

Safety
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Electrical safety
Device classifications
The Vivid 7/Vivid 7 PRO ultrasound unit is a Class I device, 
type CF, according to Sub-clause 14 of IEC 60601-1 (1988).
Inter nally connected peripheral devices
The system, together with peripheral devices, such as video 
tape recorders and printers, meets UL 2601-1 and IEC 60601-1 
(1988) standards for electrical isolation and safety. These 
standards are applicable only when the specified peripheral 
devices...

Safety
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Allergic reactions to latex-containing 
medical devices
Due to reports of severe allergic reactions to medical devices 
containing latex (natural rubber), the FDA advises health-care 
professionals to identify latex-sensitive patients, and be 
prepared to treat allergic reactions promptly. Latex is a 
component of many medical devices, including surgical and 
examination gloves, catheters, incubation tubes, anesthesia 
masks and dental dams. Patient...

Safety
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Electromagnetic Compatibility (EMC)
This unit carries the 
CE mark. The 
Vivid 7/
Vivid 7 PRO unit 
complies with regu-
latory require-
ments of the 
European Directive 
93/42/EEC con-
cerning medical de-
vices. It also 
complies with emis-
sion limits for a 
Group 1, Class B 
Medical Device as 
stated in EN 60601-
1-2 (2001) 
(IEC 60601-1-2 
(2001)).AII types of electronic equipment may characteristically cause 
electromagnetic interference with other...

Safety
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products, in the vicinity of this equipment as it may cause 
performance outside the published specifications. Keep the 
power to these types of devices turned off when near this 
equipment. 

Safety
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Environmental protection
System disposal
Please follow the disassembly procedure and part disposition 
attached inside the unit. To access to the procedure, remove 
the right side panel by unscrewing the two screws on the lower 
part. 

Safety
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