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PHYSIO-PORT / PHYSIO-PORT AS
A8136 Revision A
Electromagnetic Compatibility (EMC)
9
Appendix–Electromagnetic Compatibility (EMC)
Changes or modifications to this system not expressly
approved by PAR Medizintechnik could cause EMC
issues with this or other equipment. This system is
designed to com- ply with applicable regulations
regarding EMC. Its compliance with these requirements
has been verified. It needs to be installed and put into
service according to the EMC information stated as
follows.
Guidance and Manufacturer’s Declaration—Electromagnetic Emissions
The PHYSIO-PORT devices are intended for use in the electromagnetic environment specified below. It is the
responsibility of the customer or user to ensure that the PHYSIO-PORT devices are used in such an environment.
Emissions Test
Übereinstimmung
Elektromagnetische Umgebung – Leitlinien
RF emissions to EN 55011/
CISPR 11
Group 1
The PHYSIO-PORT devices use RF energy only for their
internal function. Therefore, their RF emissions are very
low and are not likely to cause any interference in nearby
electronic equipment.
RF emissions to EN 55011/
CISPR 11
Class B
The PHYSIO-PORT devices are suitable for use in all
establishments, including domestic and those directly
connected to the public low-voltage power supply network
that supplies buildings used for domestic purposes.
Harmonic emissions to
EN 61000-3-2/IEC 61000-3-2
not applicable
Voltage fluctuations/flicker
emissions to EN 61000-3-
3/IEC 61000-3-3
not applicable
Warning
Use of portable telephones or other radio frequency
(RF) emitting equipment near the system may
cause unexpected or adverse operation.
Warning
The equipment or system should not be used adja-
cent to, or stacked with, other equipment. If adja-
cent or stacked use is necessary, the equipment or
system should be tested to verify normal operation
in the configuration in which it is being used.
