Diemer P1800 RIDICON Manual página 113

± 2 kV for power
supply lines
Electrostatic
transient / burst
± 1 kV for
IEC 61000-4-4
input/output
lines
± 1 kV
differential
Surge
mode
IEC 61000-4-5
± 2 kV common
mode
< 5 % U
dip in U
cycle
Voltage dips,
short 40 % U
dip in U
interruptions
for 5 cycles
and voltage
variations on
70 % U
power supply
dip in U
input lines
for 25 cycles
IEC 61000-4-11
< 5 % U
(>95 % dip in
U
T
Power
frequency
(50/60 Hz)
400 A/m
magnetic field
IEC 61000-4-8
NOTE U is the a. c. mains voltage prior to application of the test level.
T
9.3 Guidance and manufacturer´s declaration – electromagnetic immunity – for
LIFE-SUPPORTING ME EQUIPMENT and ME SYSTEMS
Guidance and manufacturer´s declaration – electromagnetic immunity
The Syringe Pump is intended for use in the electromagnetic environment specified below. The customer or
the user of the Syringe Pump should assure that it is used in such an environment.
± 2 kV for
power supply
lines
± 1 kV for
input/output
lines
± 1 kV
differential
mode
± 2 kV common
mode
(>95 % < 5 %U
T T
dip in U
) for 0.5
T
0.5 cycle
(60 % 40 % U
T T
) dip in U
T
for 5 cycles
(30 % 70 % U
T
) dip in U
T
for 25 cycles
< 5
T
(>95 % dip in
)for 5 sec U )for 5 sec
T
400A/m
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.
(>95 %
)for
T
(60 %
Mains power quality should be that of a typical
)
T
commercial or hospital environment. If the user of
the Syringe Pump requires continued operation
during power mains interruptions, it is
(30 %
T
recommended that the Syringe Pump be powered
)
T
from an uninterruptible power supply or a battery.
% U
T
Power frequency magnetic fields should be at levels
characteristic of a typical location in a typical
commercial or hospital environment.
115