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11 Technical specification
CONTROL UNIT SPECIFICATION
Model
Input voltage
Output voltage
Power supply
Power consumption
Electrical classification
Fuse
Mode of operation
Cycle time
Patient pressure settings
Dimensions (L x W x H)
Weight
Sound pressure level
according EN ISO 11201
Sound power levels according
to EN ISO 3746
Environmental
IP classification
Degree of safety in presence
of inflammable anesthetics
Applied part
Ungrounded AC outlet,
electrical safety class II
CuroCell® iA Automatic
CuroCell® iA Manual
Gentle Alternating Low
Pressure
CuroCell® iA Automatic
CuroCell® iA Manual
A-weighted emission sound
pressure level LpA,eq (dB)
A-weighted sound power
level L WA (dB)
Temperature
Humidity
Atmospheric
26
CuroCell® iA Automatic, CuroCell®
iA Manual
100-240 V / 50-60 Hz / 0,6 A
12 V DC
Use only power supply with P/N
WR9QE1500LRPCIMG3138
Max 18 W
Class II, Type BF
No Fuse
Gentle Alternating Low Pressure,
and Constant Low Pressure (CLP)
10 min, 15 min, 20 min, 25 min
Automatic adjustment of patient
pressure (internal air pressure) in
the mattress
Operator sets the patient pressure
(internal air pressure) in the
mattress according to patients'
weight. Correct settings to be
controlled by hand check
11 cm x 27 cm x 15,5 cm
1,7 kg
28 dBA (at operator position)
25 dBA (at head end)
when placing the control unit on
the foot end.
<40 dBA
Operation: +5 – +40 °C
Storage: -25 – +70 °C
Transport: -25 – +70 °C
Operation: 15 % – 93 % non-
condensing
Storage: < 93 % non-condensing
700 hPa – 1060 hPa
IP42
The device is not intended for use
with flammable anaesthetic gases
Mattress
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