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MAN 01/EN/03 CRONO PAR 50 06/13
ELECTRO-MAGNETIC COMPATIBILITY
APPENDIX 7
Guide and declaration by the manufacturer - electro-magnetic emissions
CRONO PAR 50 is designed to operate in the electromagnetic environment specied below.
The client or user of the CRONO PAR 50 must ensure that it is operated in such an envi-
ronment.
Emission test Compliance Electro-magnetic environment - guide
CISPR 11 RF emissions Group 1
CRONO PAR 50 uses RF energy only for its
internal operation. As a consequence, its RF
emissions are very low and would thus not be
expected to cause any interference to electronic
devices in the vicinity.
Emissions in
RF CISPR 11
Class B
CRONO PAR 50 is designed for use in all envi-
ronments, including domestic environments and
those environments directly linked to the low vol-
tage mains supplying residential buildings.
Harmonic emissions
IEC 61000-3-2
N/A
IEC 61000-3-3 emissions
in the event of voltage
uctuations or icker
N/A
The electro-magnetic compatibility tests were performed in compliance with the
standards:
• IEC 60601-2-24:2012, Medical electrical equipment, Part 2: Particular requirements
for the safety of infusion pumps and controllers;
• IEC EN 60601-1-2 Ed. 2, Medical electrical equipment, Part 1: General requirements
for basic safety and essential performance – collateral standard: Electromagnetic
compatibility – Requirements and tests.
Guide and declaration by the manufacturer - electro-magnetic immunity
CRONO PAR 50 is designed to operate in the electromagnetic environment specied below.
The client or user of the CRONO PAR 50 must ensure that it is operated in such an envi-
ronment.
Immunity test
IEC 60601
test level
Level of
compliance
Electromagnetic environment - guide
IEC 61000-4-2
electro-static
discharge
(ESD)
15 kV in air, 8
kV on contact
15 kV in
air, 8 kV on
contact
The ooring must be wood, concrete
or ceramic. If the oor is covered in a
synthetic material, the relative humidity
must be at least 30%.
Electro-magne-
tic elds
400 A/m
50 and 60 Hz
400 A/m
50 and 60
Hz
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