Mindray BeneFusion VP3 Vet Operator's Manual page 77

Infusion pump
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If the device is operated within the electromagnetic environment listed in Table
Guidance and Declaration —Electromagnetic Immunity, the system will remain
safe and provide the following essential performance:
Operating mode
Accuracy
Function
Protection against UNINTENDED BOLUS volumes
Occlusion
ALARM CONDITIONS regarded
Data stored
Guidance and 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.
Immunity test
IEC 60601 test
level
Electrostatic
± 8 kV contact
discharge
± 15kV air
(ESD)
IEC 61000-4-2
Electrical fast
± 2 kV for power
transient/burst
supply lines
IEC 61000-4-4
± 1 kV for
input/output lines
(length greater
than 3 m)
Surge
± 1 kV line(s) to
IEC 61000-4-5
line(s)
± 2 kV line(s) to
earth
Voltage dips
0 % U
and Voltage
cycle
interruptions
IEC 61000-4-11
0 % U
and 70 % U
25/30 cycles
0 % U
cycle
Compliance level
± 8 kV contact
± 15kV air
± 2 kV for power
supply lines
± 1 kV for
input/output lines
(length greater
than 3 m)
± 1 kV line(s) to
line(s)
± 2 kV line(s) to
earth
for 0,5
0 % U
T
cycle
for 1 cycle
0 % U
T
for
and 70 % U
T
25/30 cycles
for 250/300
0 % U
T
cycle
B-3
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.
for 0,5
Mains power quality
T
should be that of a
typical commercial or
for 1 cycle
hospital environment. If
T
for
the user of our product
T
requires continued
operation during power
for 250/300
mains interruptions, it is
T
recommended that our
product be powered
from an uninterruptible

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