HEINE NC2 Manual Del Usuario página 36

Dermatoscopio
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Electromagnetic disturbances – Requirements and tests
The device is intended for use in the electromagnetic environment specified below. The customer
or the user of the device should assure that it is used in such environments.
Statement for the operational
environments
Performance features of the
ME system that have been
determined to be essential to
the performance
Warning
A list of all cables, transducers
and other accessories that are
relevant for the EMC compliance
Test
RF emissions CISPR11
Harmonic Emissions
Voltage Fluctuations/Flicker
*n/a: "Not applicable" in the internally powered mode
36/40
Inside hospitals except for: near active HF surgical equipment
and the RF shielded room of an ME system for magnetic
resonance imaging, where the intensity of EM disturbances
are high.
Use of this equipment adjacent to or stacked with other
equipment should be avoided because it could result in
improper operation. If such use is necessary, this equipment
and the other equipment should be observed to verify that
they are operating normally.
Use of accessories, transducers and cables other than those
specified or provided by the manufacturer of this equipment
could result in increased electromagnetic emissions or
decreased electromagnetic immunity of this equipment and
result in improper operation.
Portable RF communications equipment (including peripherals
such as antenna cables and external antennas) should be
used no closer than 30 cm (12 inches) to any part of the
NC2, including cables specified by the manufacturer.
Otherwise, degradation of the performance of this equipment
could result.
MED 113857
2018-02-02
None
See attachment
Compliance
Group 1
Class B
Passed*
Passed*

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Med 113857

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