Technical Description - Care of Sweden CuroCell IQ Cirrus Instructions For Use Manual

9. Technical description

9.1 Technical specification
NB: Care of Sweden reserves the right to modify the product specification at any time.
CONTROL UNIT SPECIFICATION
Model
Input voltage
Power consumption
Mode of operation
Duty cycle
Power supply
Dimensions (L x W x H)
Weight
Sound level, control unit,
max:
Environmental
Electrical classification
IP classification
Degree of safety in
presence of inflammable
anesthetics:
Applied part
MATTRESS SPECIFICATION
Model
CuroCell® Cirrus
9.2 Standards
The system is tested and approved according to the following European standards where applicable requirements are met.
IEC 60601-1 EN ISO 10993
IEC 60601-1-2 EN 12182
IEC 60601-1-11
EN 597-1
IEC 60601-1-6
EN 597-2
IEC 62304
EN ISO 14971
EN 14126
Ungrounded AC outlet, electrical safety
class II
Temperature
Humidity
Atmospheric
Dimensions (WxLxH)
80/85/90/100/105/120x200x21 cm
ISO 3746
ISO 11201
CuroCell® IQ Cirrus
100-240 V / 50-60 Hz
1.5 A
Pulsating
10 min
Use only power supply with P/N WR9QE1500LRPCIMG3138
11 cm x 30 cm x 20 cm
2.9 kg
17 dBA (at operator position), 16,5 dBA (at head end). Specifies the
highest value in accordance with EN ISO 11201:2010 when placing
the control unit on the foot end.
Operation: +5 to 40°C
Storage: -25 to 70°C
Transport: -25 to 70 °C
Operation: 15 % – 93 % non-condensing
Storage: < 93 % non-condensing
700 hPa – 1060 hPa
Class II, Type BF
IP42
The device is not intended for use with flammable anesthetic gases
Mattress
Weight
18 kg (width 85 cm)
17