Cardinal Health IVAC 571, Техническое и сервисное руководство

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IVAC® Volumetric Pump (Models 571 & 572) 86/104 1000SM00018 Issue 2
Specifications
Electromagnetic Compatibility
(continued)
Guidance and Manufacturer’s Declaration - Electromagnetic Immunity
The IVAC
®
Volumetric Pump is intended for use in the electromagnetic environment specified below.
The customer or the user of IVAC
®
Volumetric Pump should assure that it is used in such an environment.
Immunity Test
EN 60601-1-2
Test Level
Compliance Level
Electromagnetic Environment – Guidance
EN 61000-4-2
Electro-
Static Discharge (ESD)
±6 kV contact
±8 kV air ±8 kV contact (Note
2)
±15 kV air (Note 2)
Floors should be wood, concrete, or ceramic tile.
If floors are covered with synthetic material, the
relative humidity should be at least 30 %.
EN 61000-4-4
Electrical Fast Transient,
Burst (EFT) (Note 3)
±2 kV for power
supply lines
±1 kV for input/
output lines
±2 kV for power
supply lines
N/A (Note 4)
Mains power quality should be that of a typical
commercial or hospital environment.
EN 61000-4-5
Power Line Surge
(Note 3)
±1 kV Line(s) to
Line(s)
±2 kV Line(s) to
Earth
±1 kV Line(s) to
Line(s)
±2 kV Line(s) to
Earth
Mains power quality should be that of a typical
commercial or hospital environment.
EN 61000-4-8 Power
Frequency Magnetic Field
(50/60 Hz)
3 A/m 400 A/m 50 Hz
(Note 2)
Power frequency magnetic fields should be at
levels characteristic of a typical location in a
typical commercial or hospital environment.
EN 61000-4-11
Voltage Dips, Short
Interruptions, and Voltage
Variations
(Note 3)
<5 %
U
T (Note 1)
(>95 % dip in
U
T)
for 0.5 cycle
<5 %
U
T
(>95 % dip in
U
T)
for 0.5 cycle
Mains power quality should be that of a typical
commercial or hospital environment.
If the user of the pump requires continued
operation during power mains interruptions, it is
recommended that the pump be powered from
an uninterruptible power supply or a battery.
The pump does employ an internal short
duration battery.
40 %
U
T
(60 % dip in
U
T)
for 5 cycles
40 %
U
T
(60 % dip in
U
T)
for 5 cycles
70 % U T
(30 % dip in
U
T)
for 25 cycles
70 % U T
(30 % dip in
U
T)
for 25 cycles
<5 %
U
T
(>95 % dip in
U
T)
for 5 sec
<5 %
U
T
(>95 % dip in
U
T)
for 5 sec
Note 1—
U
T
is the AC mains voltage prior to application of the test level.
Note 2—Compliance levels raised by EN 60601-2-24.
Note 3—Performed at the Minimum and Maximum Rated Input Voltage.
Note 4—Cardinal Health recommends using signal cables of less than 3 meters in length and this requirement is applicable only if signal cables are 3
meters or more in length. (EN 60601-1-2:2002, Clause 36.202.4)