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Guidance and Manufacturer’s Declaration - Electromagnetic Immunity
The CEFAR BASIC Electrotherapy System is intended for use in the electromagnetic environment specified below. The customer
or the user of the CEFAR BASIC Electrotherapy System should assure that it is used in such an environment
Immunity Test IEC 60601
Test Level Compliance Level Electromagnetic Environment -
Guidance
Electrostatic discharge
(ESD) IEC 61000-4-2
±6kV contact
±8kV air
±6kV contact
±8kV air
Risk assessment on the CEFAR
BASIC Electrotherapy System
indicates the compliance levels
claimed are acceptable when ESD-
precautionary measures are taken.
Electrical fast transient/
burst IEC 61000-4-4
±2kV for power supply lines
±1kV for input/output lines
Not Applicable - Battery
powered
Not Applicable - signal lines
less then 3 meters
Mains power quality should be
that of a typical commercial or
hospital environment.
Surge
IEC 61000-4-5
+ 1kV dierential mode (line
to line)
+ 2kV common mode (line
to ground)
Not Applicable - Battery
powered
Mains power quality should be
that of a typical commercial or
hospital environment.
Voltage dips, short
interruptions and voltage
variations on power supply
input lines
IEC 61000-4-11
<5% UT (>95% dip in UT) for
0,5 cycle
40% UT (60% dip in UT) for
5 cycles
70% UT (30% dip in UT) for
25 cycles
<5% UT (>95% dip in UT) for
5 sec
Not Applicable - Battery
powered
Mains power quality should be
that of a typical commercial or
hospital environment. If the user
of the CEFAR BASIC Electrotherapy
System requires continued
operation during power mains
interruptions, it is recommended
that the CEFAR BASIC Electro-
therapy System be powered from
an uninterrupted power supply.
Power frequency
(50/60Hz) magnetic field
IEC 61000-4-8
3 A/m 3 A/m Power frequency magnetic
fields should be at levels
characteristic of a typical location
in a typical commercial or hospital
environment.
NOTE: UT is the AC mains voltage prior to application of the test level.
53


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