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EN
20
Guidance and Manufacturer’s Declaration – Electromagnetic Immunity
The Bone Growth Stimulator is intended for use in the electromagnetic environment
specified below. The customer or the user of the Bone Growth Stimulator 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
±2kV, ±4kV,
±6kV contact
±2kV, ±4kV,
±8kV air
±2kV, ±4kV,
±6kV contact
±2kV, ±4kV,
±8kV air
Floors should be wood,
concrete or ceramic tile.
If floors are covered
with synthetic material,
the relative humidity
should
be at least 30%.
Electrical Fast
Transient/Burst
IEC 61000-4-4
N/A
N/A
N/A
Surge
IEC 61000-4-5
N/A
N/A
N/A
Voltage
dips, short
interruptions
and voltage
variations on
power supply
input lines
IEC 61000-4-11
N/A
N/A
N/A
Power Frequency
(50/60Hz)
Magnetic Fields
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:
U
T
is the a.c mains voltage prior to application of the test level.