Emc Details - Enraf Nonius Endopuls 811 Manual Del Usuario

17 EMC details

Medical electrical devices such as the Endopuls 811are 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.
The Endopuls 811 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 Endopuls 811 is intended for operation in an electromagnetic environment as
indicated below. The customer or user of the Endopuls 811 should ensure that it is operated in
such an environment.
Interference tests
RF emissions according to CISPR 11 Group 1
RF emissions according to CISPR 11 Class A
Harmonic emissions according to
IEC 61000-3-2
Voltage fluctuation emissions and
flicker according to IEC 61000-3-3
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.
Conformity Electromagnetic environment
guideline
The device Endopuls 811 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.
The device Endopuls 811 is suitable
for use in all installations including
Class A
those in a residential environment
and those which are directly
connected to the public mains
Conforms
network which also supplies buildings
which are used for residential
purposes.
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