GE SENOGRAPHE 800T Operator's Manual page 7

GE Medical Systems
REV 6
Note:
REGULATORY REQUIREMENTS
This equipment generates, uses, and can radiate radio frequency energy. The equipment
may cause radio frequency interference to other medical and non-medical devices and
radio communications. To provide reasonable protection against such interference, this
product complies with emission limits for Group 1 Class A Medical Devices as stated in
EN 60601–1–2.
However, there is no guarantee that interference will not occur in a particular installation. If
this equipment is found to cause interference (which may be determined by switching the
equipment on and off), the user (or qualified service personnel) should attempt to correct the
problem using one or more of the following measures:
D
Reorientate or relocate the affected device(s).
D
Increase the separating space between the equipment and the affected device.
D
Power the equipment from a source different from that of the affected device.
D
Consult the point of purchase or the service representative for further suggestions.
The manufacturer is not responsible for any interference caused either by the use of
interconnect cables other than those recommended or by unauthorized changes or
modifications to this equipment. Unauthorized changes or modifications could void the
user's authority to operate the equipment.
To comply with the regulations applicable to an electromagnetic interface for a Group 1
Class A Medical Device, all interconnect cables to peripheral devices must be shielded and
properly grounded. Use of cables not properly shielded and grounded may result in the
equipment causing radio frequency interference in violation of the European Union
Medical Device directive and FCC regulations.
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SENOGRAPHE 800T
om 2135575–100