AGFA DX-D 300 User Manual page 37

2.8 ELECTROMAGNETIC COMPATIBILITY (EMC)
0171F EN 20181009
This equipment generates, uses, and can radiate radio frequency energy.
The equipment may cause radio frequency interference to
other medical or non medical devices and to radio
communications.
To provide reasonable protection against such interference, this equipment
complies with emissions limits for a Group 1 -- Class A Medical Devices
Directive as stated in IEC 60601--1--2: 2007 and 2014. 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
turning the equipment on and off), the operator (or qualified service personnel)
should attempt to correct the problem by one or more of the following measures:
reorient or relocate the affected device,

increase the separation between the equipment and the affected device,

power the equipment from a source different from that of the affected

device,
consult the service engineers for further suggestions.

To comply with the regulations applicable to an electromagnetic interference 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
of Federal Communications Commission regulations.
Before using this equipment make sure that all requirements
about EMC included in this manual are accomplished.
Should any interference (EMC) be detected with other
equipment, please position other equipment away from this
one.
DX-D 300 U-Arm
User Manual
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