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Copyright © 2020 Ultrasound Technologies Ltd
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Table 2: Guidance and Manufacturer’s Declaration - Electromagnetic Immunity
The MedicCO
2
LON device is intended for use within the electromagnetic environment specified below.
The customer or the operator of a MedicCO
2
LON Insufflator should ensure that it is used within such an
environment.
Immunity Test
IEC 60601
Test Level
Compliance Level
Electromagnetic environment
Guidance
Electrostatic discharge
(ESD) IEC 61000-4-2
± 8 kV contact
± 15 kV air
± 8 kV contact
± 15 kV 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
± 2 kV for power
supply lines
± 1 kV for input/
output lines
± 2 kV for power
supply lines
± 1 kV for input/
output lines
Mains power quality should be that
of a typical commercial or hospital
environment.
Surge IEC 61000-4-5
± 1 kV differential
mode
± 2 kV common
mode
± 1 kV differential
mode
± 2 kV common
mode
Mains power quality should be that
of a typical commercial or hospital
environment.
Power frequency
(50/60 Hz) 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.
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 seconds
<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 seconds
Mains power quality should be that
of a typical commercial or hospital
environment. If the operator
of the MedicCO2LON device
requires continued operation
during power mains interruptions,
it is recommended that the
MedicCO2LON device be powered
from an uninterruptible power
supply.
Note: Ut is the a.c. mains voltage prior to application of the test level.
7. EQUIPMENT
SPECIFICATION
