Drive DeVilbiss Healthcare Elite, Руководство пользователя

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Elite Mattress with PUMP1000 12
Technical Description
Pump Specification
Power Supply 220-240V 50-60Hz 0.07A 16W
Fuse Rating T1A / 250v
Cycle Time 10 minutes
Dimensions 291 x 200 x117 (mm)
Weight 2.8kg
Modes Alternating, Static & Cushion
Air Output 8 litres per minute
Pressure Range 15mmHg – 40mmHg±10%
Environment
Temperature Operation 10°C to 40°C (50°F to 104°F)
Storage -15°C to 50°C (5°F to 122°F)
Shipping -15°C to 70°C (5°F to 158°F)
Humidity Operation 20% to 90% (non-condensing)
Storage: 10% to 90% (non-condensing)
Shipping: 10% to 90% (non-condensing)
• Not suitable for use in the presence of a flammable anaesthetic mixture (No AP or APG protection)
Noise Level 30 dB
Classification
o
Class I medical device
o
Type BF
Electrical classification Class II
Ingress Protection • IP21 (Protection against fingers or other object not greater than 80mm
in length and 12mm in diameter) & (Vertically dripping water shall have
no harmful effect when the enclosure is tilted at an angle of 15° from its
normal position)
Applied Part • Elite Mattress & Elite Cushion
Usage • Continuous operation
Mattress Specification
Dimensions 1880 x 890 x175mm
Weight 6Kg
Max Patient Weight 190kg
Top Cover Material Xtreme fabric (PU coated fabric substrate)
Cell Material Nylon / PVC
Cell Configuration 16 single cell formation
Fire Classification BS5852 / BS7175 composite – (Risk assessment to be carried out)
Risk Factor Very High Risk with pump
Electromagnetic Interference
•
This device has been tested to withstand electromagnetic interference (EMI) from
commonly found electrical equipment.
•
EMI can affect some types of electronic medical devices (such as pacemakers, defibrillators,
ECG monitors and infusion pumps). If in any doubt before use, a risk assessment should be
carried out before using this or any other electrical device around sensitive devices.
•
Electrical equipment may be susceptible to EMI from sources such as mobile phones, walkie-
talkies, TV broadcast and emergen
cy services’ radio. A risk assessment should also be carried
out before using electronic medical devices in areas close to these sources.
•
The addition of components or accessories may affect the EMI susceptibility of the device.
Do not fit accessories other than Drive DeVilbiss Healthcare authorised accessories.