Technical Part; Information - Invacare ScanBed 750 Manual Del Usuario

Technical part

Invacare® is certified according to DS/EN ISO 9001 and ISO 13485 which ensures that our
customers are always supplied with Invacare® products of uniform quality.
Throughout the entire production process our materials and products are quality controlled by the operators.
Furthermore there is a final test when the product is fully assembled.
The operator carrying out the final test, which comprises of checking 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® 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

Please read the entire technical information section carefully before using or servicing the bed.
All indications of right and left are based on a patient lying on his back in the bed.
Please note that there may be sections in this User's Manual, which are not relevant for your bed.
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The SB750 is CE-marked in accordance with directive 93/42/EEC concerning Medical Apparatus.
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The SB750 is tested without remarks by HMI according to EN 1970.
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SB750 is tested and approved in accordance with NF (Norme Francaise).
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SB750 TM is EMC tested and approved in accordance with EN 60601-1-2:93 by UL Demko.
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The motors and control unit of the SB750
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SB750 has undergone a risk analysis according to EN 14971.
Max. patient weight: 185 kg.
The hand control, control unit and motors are protected according to IP 66.
A lock cam must be used on the control unit - if not, Invacare®cannot guarantee the IP protection.
Electromagnetic interference between the bed and other electrical products can occur.
To reduce or eliminate such electromagnetic interference, increase the distance between the bed
and the products or switch them off.
This medical bed can be used together with medical electrical equipment connected to the heart
(intracardially) or the blood vessels (intravascularly), provided that following points are respected:
- The medical bed should be equipped with means for potential equalization connection marked
out by a symbol shown in the back of this manual.
- Medical electrical equipment should not be fixed on the bed's metallic accessories
such as side rails, lifting pole, drip rod, bed ends ect.
In addition, the medical electrical equipment power supply cord should be kept clear
of the accessories or any other moving part of the bed.
Invacare®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 11.
TM
are approved according to EN 60601:1996-03.
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QA XXX