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Terraillon Tensio Instruction Manual page 77

Wrist blood pressure monitor
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Table 2 – Guidance and MANUFACTURER'S declaration – electromagnetic IMMUNITY – for all ME EQUIPMENT
and ME SYSTEMS
ME
IMMUNITY test
Electrostatic
discharge (ESD)
IEC 61000-4-2
.
ly
Electrical fast
nt
transient/burst
IEC 61000-4-4
Surge
IEC 61000-4-5
Voltage dips,
short interruptions
and voltage
variations
on power supply
input lines
IEC 61000-4-11
Power frequency
(50/60 Hz)
magnetic field
IEC 61000-4-8
Guidance and manufacturer's declaration – electromagnetic immunity
The device is intended for use in the electromagnetic environment specified below.
The customer or the user of the device should assure that it is used in such an environment.
IEC 60601- test level
± 6 kV contact
± 8 kV air
± 2 kV for power supply lines
± 1 kV for input/output lines
± 1 kV line(s) to line(s)
± 2 kV line(s) to earth
<5 %
(>95 % dip in
for 0,5 cycle
40 %
(60 % dip in
for 5 cycles
70 %
(30 % dip in
for 25 cycles
<5 %
(>95 % dip in
for 5 s
3 A/m
NOTE
is the a.c. mains voltage prior to application of the test level.
Compliance level
± 6 kV contact
± 8 kV air
Not applicable
Not applicable
)
)
Not applicable
)
)
3 A/m
Electromagnetic environment –
guidance
Floors should be wood, concrete or
ceramic tile. If floors are covered with
synthetic material,
the relative humidity should be at
least 30 %.
Mains power quality should be that
of a typical commercial or hospital
environment.
Mains power quality should be that
of a typical commercial or hospital
environment.
Mains power quality should be that
of a typical commercial or hospital
environment. If the user of the device
requires continued operation
during power mains interruptions,
it is recommended that the device
be powered from an uninterruptible
power supply or a battery.
Power frequency magnetic fields
should be at levels characteristic
of a typical location in a typical
commercial or hospital environment.
77

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