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9 Technical specification
CuroCell UNO®
Model
Input voltage
Power consumption
Fuse
Mode of operation
Duty cycle
Power supply
Dimensions (L x W x H)
Weight
Sound level, control unit,
max
Environmental
Backup battery (option)
Electrical classification
IP classification
Degree of safety in presence
of inflammable anastethics
Applied part
9.1
Standards
The system has been tested and approved according to following standards where applicable
demands are fulfilled:
IEC 600601‐1
EN 597‐1
IEC 60601-1-2
EN 597-2
IEC 60601‐1-11
EN 12182
(Pulsating and alternating)
Ungrounded AC outlet,
electrical safety class II
Temperature
Version with backup
battery
Humidity
Atmospheric
EN ISO 10993
EN ISO 14971
17
CuroCell UNO®
100‐240 V / 50‐60 Hz
15A
No Fuse
Constant low pressure, Pulsating and
Alternating
10 min, 15 min, 20 min, 25 min
Use only power supply with P/N
RR9KE5000LRPYIMG2806
15,6 cm x 38,7 cm x 25,1 cm
5.2 kg (fully equipped)
EN ISO 11201:2010 -20 dBA (at operator
position), 18 dBA (at head end). ISO
3746:2010 -40 dBA.
Operation: +5 °C – 40 °C
Storage: ‐ 25 °C – 70 °C
Storage: ‐ 20 °C – 45 °C
Transport: ‐ 25 °C – 70 °C
Operation: 15 % – 93 % non‐condensing
Storage: < 93 % non‐condensing
700 hPa – 1060 hPa
10 x Ni‐MH, 1.2 V, 3500 mAh
Class I, Class II, Type BF
IP42
The device is not intended for use with
flammable anaesthetic gases
Mattress
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