9. Technical description
Control unit
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 anaesthetics:
Applied part
Model
Dimensions (WxLxH)
Weight
SPECIFICATION
CuroCell UNO®
100‐240 V / 50‐60 Hz
1.5 A
No Fuse
Constant low pressure, Pulsating and Alternating
10 min, 15 min, 20 min, 25 min
Use only power supply with P/N RR9KE5000LRPYIMG2806
Use only power supply with P/N RR9LE5000LRPYIMG2768
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
SPECIFICATION
CuroCell UNO®
80/85/90/105/120 x 200/210/220 x 20 cm
11 kg (80x200 cm)
(Pulsating and Alternating)
Ungrounded AC outlet,
electrical safety class II
Grounded AC outlet, electri‐
cal safety class I
Temperature
Version with backup battery
Humidity
Atmospheric
9.1 Technical specification
NB:
Care of Sweden reserves the right to modify the product specification at any time.
WARNING
Follow the operation and maintenance instructions carefully in order to prevent physical injury, as well as damage to the product or other
equipment.
9.2 Standards
The system has been tested and approved according to the following standards:
IEC 600601‐1
EN ISO 10993
EN 597‐1
EN ISO 14971
IEC 60601‐1‐2
EN 12182
EN 597‐2
IEC 60601‐1‐11
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