Table of Contents
Advertisement
Technical information
Invacare®EC-Høng A/S is certified according to DS/EN ISO 9001/ISO 13485 which ensures that our customers
are always supplied with Invacare®EC-Høng A/S products of uniform quality.
Throughout the entire production process our materials/products are quality controlled by the operators.
Furthermore there is a final test when the product is fully assembled.
The operator carries out the final test, which comprises a check of all
moveable parts, motors/gas springs and castors, issues a QA number on the
product thereby confirming its quality.
If the product does not correspond to the quality demands of Invacare®EC-Høng A/S, it will be discarded.
If, contrary to our expectations, a problem should arise in connection with the delivered product, please
contact your Invacare®supplier.
3. Information
Approvals
•
Invacare®Octave is
medical devices.
•
Invacare®Octave has undergone a risk analysis according to NF EN 14971.
•
Invacare®Octave is approved to carry a max. load of: 385 kg incl. equipment.
Max. patient weight: 350 kg (Only if the equipment - bedend. siderail, support handle, lifting pole and mattress
- weight max. 35 kg).
Control units and motors are protected according to IP 66.
If an electronic part has IP 66 protection, the lock cam of the control unit must be used, otherwise
Invacare®EC-Høng A/S provides no guarantee for the protection.
4. General Information
Invacare®EC-Høng A/S accepts no liability for any use, change or assembly of the product other
than as stated in this User's Manual.
If the functions of the bed change, please send the bed immediately for a check-up according to the maintenance
chart, chapter 10.
The Invacare®Octave must be stored in a room with a humidity equivalent to normal indoor conditions. The bed
must be stored in a frost-free environment.
-marked in accordance with Directive 93/42/EEC of 27 February 2002 concerning
8
QA XXX
Advertisement
Table of Contents
