Manufacturer’s declaration of
Electromagnetic Compatibility
15
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Medical electrical devices such as en
Puls
Version 2.0 are subject to special precautions with regard to electromagnetic
compatibility (EMC) and must be installed and commissioned in accordance with the EMC advice given in the instructions for
use and accompanying documents.
Portable and mobile RF communication systems (e.g. mobile phones) may interfere with medical electrical equipment.
en
Puls
Version 2.0 should only be operated with the original mains cable specified in the list of contents delivered.
Operating the device with any other mains cable can lead to increased emissions or reduced interference immunity of the
device.
Guidelines and manufacturer's declaration – electromagnetic interference
The device en
Puls
Version 2.0 is intended for operation in an electromagnetic environment as indicated below. The
customer or user of the en
Puls
Version 2.0 should ensure that it is operated in such an environment.
Interference tests
Conformity
Electromagnetic environment guideline
RF emissions according to CISPR 11
Group 1
The device en
Puls
Version 2.0 uses RF
energy solely for its internal functioning. Its RF
emission is therefore very low and it is unlikely
that this will cause interference to
neighbouring electronic equipment.
RF emissions according to CISPR 11
Class A
Harmonic emissions according to IEC
61000-3-2
Class A
Voltage fluctuation emissions and flicker
according to IEC 61000-3-3
Conforms
The device en
Puls
Version 2.0 is suitable for
use in all installations including those in a
residential environment and those which are
directly connected to the public mains network
which also supplies buildings which are used
for residential purposes.
The device should not be used when placed immediately next to or stacked on top of other devices. If operation is necessary
when immediately next to or stacked on top of other devices, the device should be monitored to ensure it is operating as
intended in this arrangement.
Содержание enPuls
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