Mindray DPM 1 Manuel de l'opérateur Page 93

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B-1
B EMC
The device meets the requirements of IEC60601-1-2.
NOTE
Use of accessories, transducers, and cables other than those specified may result
in increased emission and/or decreased electromagnetic immunity of the patient
monitoring equipment.
The device or its components should not be used adjacent to or stacked with
other equipment. and if adjacent or stacked use is necessary, the equipment
should be observed to verify normal operation in the configuration in which it
will be used.
The equipment needs special precautions regarding EMC and needs to be
installed and put into service according to the EMC information provided
below.
Other devices may affect this monitor even though they meet the requirements
of CISPR.
When the inputted signal is below the minimum amplitude provided in technical
specifications, erroneous measurements could result.
Portable and mobile RF communications equipment may affect this equipment.
Guidance and Declaration - Electromagnetic Emissions
The device is suitable for use in the electromagnetic environment specified below. The
customer or the user of the device should assure that it is used in such an environment.
Emission tests Compliance Electromagnetic environment - guidance
RF emissions
CISPR 11
Group 1 The equipment uses RF energy only for its internal
function. Therefore, its RF emissions are very low
and are not likely to cause any interference in nearby
electronic equipment.
RF emissions
CISPR 11
Class A
Harmonic Emissions
IEC61000-3-2
Class A
Voltage
Fluctuations/Flicker
Emissions
IEC 61000-3-3
Compliance
The equipment is suitable for use in all
establishments other than domestic and those
directly connected to the public low-voltage power
supply network that supplies buildings used for
domestic purposes.
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