OLA 8 & 4 provide regular periods of pressure reduction to vulnerable tissue INTRODUCTION areas, aiding blood and lymphatic flow which is vital to maintaining healthy tissue.
OLA 8 Control Unit (Q2-02): • Do not use the control unit near flammable gas or in oxygen rich • Audible low pressure alert environments as this poses a fire risk or risk of explosion. • Pressure adjustment for optimum therapy •...
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(e.g. mains cable) – If damage Do not fold. Roll pack the system is noticed to the control unit or mains cable assembly turn off at the mains supply and contact your provider or Select Medical Ltd. immediately. Do not use sharp objects...
2. Air Cells Control Unit 3. Male Air Connector 4. Base Cover OLA 8 - Q2-02 Control Unit OLA 4 - D30 Control Unit 5. Securing Straps (elasticated corner straps only on OLA 4) 1. Control Panel 1. Control Panel 6.
2). caution notes carefully. These highlight risk areas to ensure patient 3. Place the mattress on top of the bed frame (OLA 8), or on top of the safety. existing mattress (OLA 4), with the top cover facing upwards and the air hose at the foot end of the bed.
2. The low pressure indicator (orange) will illuminate as inflation commences. 4. Normal Pressure Indicator 3. OLA 8 /Q2-02 only - the audible alert is activated, press the ‘alert mute’ A visible indicator (green) identifies that the pressure has reached the button to mute the alarm and its indicator will flash.
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‘low pressure’ indicator (and audible Incontinence products, such as sheets or pads, can be used with the system, alarm on the OLA 8/Q2-02 ) will turn off. however this may compromise the effectiveness of the alternating pressure distribution.
1. Check for external damage – do not use if damage is found. • The mattress will remain inflated for up to 24 hours - return the system to the mains supply as soon as possible. 2. Place the pump on a work surface and using a clean cloth wipe the outside •...
General Cleaning: 5. Store in a sealed polythene bag to protect from dirt, debris, fluids etc. with 1. Wipe down with a clean cloth moistened with a mild detergent and diluted a suitable identification tag. in warm water (40˚C). 6. Store the control unit in a separate, sealed polythene bag to protect from 2.
Only Select Medical approved components specified for OLA 8 & silence the power failure indication). 4 are to be used - if in doubt contact Select Medical Ltd or your 2. Check the mains socket is working - plug in a device that is local distributor.
When the electrical system has come to the end of its useful life, contact your Maximum Patient Weight: OLA 8: 190kg (30 stone) provider or Select Medical Ltd. (see pg 2) to arrange for collection, OLA 4: 114kg (18 stone) alternatively follow local recycling and W.E.E.E. (Waste Electrical and No.
Requirements according to IEC 60601-1-2:2007 ELECTROMAGNETIC COMPATIBILITY OLA 8 & 4 are intended for use in the electromagnetic environment specified below. The control unit has been designed to meet the EMC requirements of IEC 60601-1-2:2007. This standard defines the levels of immunity to •...
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If the measured field strength in the location in which the or hospital OLA 8 or 4 is used exceeds the applicable RF compliance level above, OLA 8 or 4 should environment. be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as re-orienteering or relocating the system.
OLA 8 & 4 are intended for use in an electromagnetic environment in which WARRANTY & SERVICE radiated RF disturbances are controlled. The customer/user of OLA 8 or 4 can help prevent electromagnetic interference by maintaining a minimum • Select Medical Ltd guarantees this equipment under normal use for a...
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Contact Information T: 01254 668899 | E: sales@selectmedical.co.uk www.selectmedical.co.uk Registered in England No. 4281283 | VAT Reg No. 785 7314 91...
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