Emc Declaration - Diemer P1800 RIDICON Manual

9 EMC Declaration

The pump accord with EMC IEC60601-1-2.
9.1 Guidance and manufacturer´s declaration – electromagnetic emission – for all
EQUIPMENT AND SYSTEMS
1 Guidance and manufacturer´s declaration – electromagnetic emission
The Syringe Pump is intended for use in the electromagnetic environment specified below. The
2
customer or the user of Syringe Pump should assure that it is used in such an environment.
3 Emissions test
RF emissions
4
CISPR 11
RF emissions
5
CISPR 11
Harmonic
6 emissions
IEC 61000-3-2
Voltage
fluctuations /
7
flicker emissions
IEC 61000-3-3
9.2 Guidance and manufacturer's declaration – electromagnetic immunity – for all
EQUIPMENT and SYSTEMS
Guidance and manufacturer´s declaration – electromagnetic immunity
The Syringe Pump is intended for use in the electromagnetic environment specified below. The customer or
the user of the Syringe Pump should assure that it is used in such an environment.
EN 60601
Immunity test
test level
Electrostatic
± 8kV contact
discharge (ESD)
± 15kV air
IEC 61000-4-2
Compliance Electromagnetic environment - guidance
The Syringe Pump uses RF energy only for its internal function.
Group 1 Therefore, its RF emissions are very low and are not likely to
cause any interference in nearby electronic equipment.
Class B
The Syringe Pump System is suitable for use in all establishments,
Class A
including domestic establishments and those directly connected to
the public low-voltage power supply network that supplies
buildings used for domestic purposes.
Complies
Compliance
level
± 8 kV contact
± 15 kV air
Electromagnetic environment -
guidance
Floors should be wood, concrete or ceramic tile. If
floors are covered with synthetic material, the
relative humidity should be at least 30 %.
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