Drive DeVilbiss Healthcare Hybrid-Power, Руководство пользователя

Страница: 16 / 18

15 – Hybrid-Power
Technical Description
Pump Specification
Power Supply 220-240V 50-60Hz 0.25A 16W
Fuse Rating T1A / 250v
Cycle Time 10 minutes
Dimensions 310 x 210 x 125 (mm)
Weight 2.5kg
Modes Alternating & Static
Air Output 8 litres per minute
Pressure Range 15mmHg – 40mmHg±10%
Environment
Temperature Operation 10°C to 35°C (50°F to 95°F)
Storage -15°C to 50°C (5°F to 122°F)
Shipping -15°C to 70°C (5°F to 122°F)
Humidity Operation 20% to 80% (non-condensing)
Storage: 10% to 90% (non-condensing)
Shipping: 10% to 90% (non-condensing)
x Not suitable for use in the presence of a flammable anaesthetic mixture (No AP or APG protection)
Noise Level 30 dB
Classification
o
Class IIa medical device (in accordance with the Medical Device
Directive 93/42/EEC)
o
Type BF
Electrical classification Class I Protective Earth
Ingress Protection x 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 x Hybrid-Power Mattress
Usage x Continuous operation
Mattress Specification
Dimensions 1980 x 880 x160mm
Weight 16Kg
Max Patient Weight 254kg with a pump
Top Cover Material Xtreme fabric (PU coated fabric substrate)
Cell Material PU / Silicon
Cell Configuration 14 foam filled single cell formation
Fire Classification Complies with BS7177 –
(Risk assessment to be carried out by care provider)
Risk Factor Very High Risk with pump / Medium to High without the pump
Electromagnetic Interference
x
This device has been tested to withstand electromagnetic interference (EMI) from
commonly found electrical equipment.
x
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.
x
Electrical equipment may be susceptible to EMI from sources such as mobile phones, walkie-
talkies, TV broadcast and emergency services’ radio. A risk assessment should also be carried
out before using electronic medical devices in areas close to these sources.
x
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.