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www.medicalsuction.co.uk
5
Guidance and manufacturer’s declaration Electromagnetic Immunity
The surgical aspiratorNEW ASKIR 230/12V BR is intended for use in the electromagnetic environment specified
below.
The customers or the user of the surgical aspirator NEW ASKIR 230/12V BR should assure that it’s used in such an
environment.
Immunity Test Compliance Electromagnetic environments -
guidance
Electrostatic discharge (ESD)
IEC/EN 61000-4-2
± 6kV on contact
± 8kV in 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/EN 61000-4-4
± 2kV power supply
Mains power quality should be that of
a typical
commercial environment or hospital
Surge
IEC/EN 61000-4-5
± 1kV differential mode
Mains power quality should be that of
a typical
commercial environment or hospital
Loss of voltage, brief voltage
interruptions and variations
IEC/EN 61000-4-11
5%U
T
for 0.5 cycle
40%U
T
for 05 cycle
70%U
T
for 25 cycle
<5%U
T
for 5 sec
Mains power quality should be that of
a
typical commercial environment or
hospital If
the user of the surgical aspirator NEW
ASKIR 230/12V BR request that the
appliance operates
continuously, the use of a continuity
unit is
recommended.
Magnetic field
IEC/EN 61000-4-8
3A/m
The power frequency magnetic field
should be
measured in the intended installation
location to
assure that it’s sufficiently low.
Conducted Immunity
IEC/EN 61000-4-6
3Vrms 150kHz to 80MHz
(for appliances that aren’t life -
supporting)
-
Irradiated Conducted
IEC/EN 61000-4-3
3V/m 80MHz to 2.5 GHz
(for appliances that aren’t life -
equipment)
-
Note U
T
is the value of the power supply voltage
ACCESSORIES SUPPLIED
DESCRIPTION
COMPLETE ASPIRATION JAR 1000cc
CONICAL FITTING
TUBES SET 6 mm x 10 mm
ASPIRATION PROBE CH20
ANTIBACTERIAL FILTER
Antibacterial Filter: The filter is produced with (PTFE) hydrophobic material to prevent fluids entering the pneumatic
circuit. It should be changed immediately if it becomes
wet or if there is any sign of contamination or discolouration. If should also be changed if the unit is used with a
patient whose risk of contamination is
unknown. Don’t use the suction unit without the protection filter. If the suction unit is used in an emergency or in a
patient where the risk of
contamination is not know the filter must be changed after each use. Available under request with different versions
with complete jar 2000cc.
Suction catheter: Single-use device to be used on a single patient. Do not wash or re-sterilize after use.
Reuse may cause cross-infections. Don’t use after lapse of the sell-by date
5


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