Remarks For Hf-Emission And Immunity - AGFA DX-D 300 User Manual

Remarks for HF-emission and immunity

This equipment generates, uses, and can radiate radio frequency energy.
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. 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.
DX-D 300 | Remarks for HF-emission and immunity | 79
CAUTION:
The equipment may cause radio frequency interference to other
medical or non medical devices and to radio communications.
CAUTION:
Before using this equipment make sure that all requirements
about EMC included in this manual are accomplished.
CAUTION:
Should any interference (EMC) be detected with other
equipment, please position other equipment away from this one.
CAUTION:
It is customer responsibility to assure that this equipment and
vicinity equipment complies the value of radio frequency
0172E EN 20181116 1653