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105
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 specied 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 specied 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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