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Summary of Contents for Accora Altida Plus
- Page 1 Altida Plus Instruction Manual V E R S I O N T H R E E O C T O B E R 2 0 1 5...
- Page 2 The noise levels do not exceed 70Db (A). The Altida Plus adjustable nursing bed is designed to be If using the electronic functions could affect used by patients in both low and high need care...
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Page 3: Safety Instructions
The bed may not be used if faults have been detected on it that It is essential to consult Accora in advance if you wish to use may injure the patient, staff or a third person, the bed or the the bed for any purpose outside the use detailed in this surroundings. -
Page 4: Technical Specification
Side rail height above the mattress platform (without the 75mm mattress) at the lowest height Safe Working Load 180kg Maximum Patient Weight (using a typical mattress of 170kg 20kg and any additional accessories) © Accora: 01223 206100 | info@accora.uk.com | www.accora.uk.com... - Page 5 See Figure 4. Note that there are two handscrews each side at the footboard end of the bed to allow for a bed extension if required. © Accora: 01223 206100 | info@accora.uk.com | www.accora.uk.com...
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Page 6: Bed Positioning
105mm, although the safe place at the foot end of the bed. operator would normally adjust the bed height from the sides of the bed. © Accora: 01223 206100 | info@accora.uk.com | www.accora.uk.com... -
Page 7: Cleaning And Disinfection
Lifting Equipment All parts of the mattress Operations Regulations (LOLER) so there is no formal legal requirement for regular inspection by a competent person. Accessible metal parts on the mattress platform © Accora: 01223 206100 | info@accora.uk.com | www.accora.uk.com... - Page 8 If any serious fault is encountered during regular maintenance, the bed must not be used any further. If you experience any problems with this product, please contact the company who supplied you or Accora. 15. Daily Maintenance The daily maintenance work can be performed by the nursing personnel or carer: ...
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Page 9: Ec Declaration Of Conformity
Refer to product label conforms to the Requirements of Directive 93/42/EEC relating to Medical Devices Class 1 Product. Signed by: Name: Laurie Drake Position: Operations Director Done at: Cambridge Date of Validity: 03/02/15 © Accora: 01223 206100 | info@accora.uk.com | www.accora.uk.com... - Page 10 IFU-AL1-002EN Rev 03 © Accora: 01223 206100 | info@accora.uk.com | www.accora.uk.com...
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