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HEPRO Standard Series - Page 4

HEPRO Standard Series
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SERVICE MANUAL for
Work Chairs, Coxit-chairs and Standing support chairs
4
HEPRO aid manufacturer
HEPRO is a Norwegian industrial company that develops, manufactures and sells technical aids for adults and children
with mobility impairment. The company was established in 1987 and has today about 30 employees. The company`s
head quarter and factory is located in Rognan, Nordland: Hepro AS, Øvermoan 9, 8250 Rognan, N-Norway. Phone +47
46 74 55 55.
Technical Service
Services are performed in the factory at Rognan, but also by partners in many parts of the country. Our sales
personnel are also trained in technical maintenance. By defect of the products or other queries, please contact your
distributor or importer.
Warranty
When used in accordance with the Operating Instructions and the User Reference Manual, Hepro provides a two-year
warranty against defects in material and workmanship. Please address warranty complaints or other inquiries about
the product to your distributer or importer. Always state the product`s serial number as a reference.
The product is designed, tested and produced in conformity to following regulations and requirements:
NS-EN 12182
Technical aids for disabled persons General requirements and test methods”.
NS-EN 1335-1
Office work chair. Dimensions Determination of dimensions.
NS-EN 1335-2
Office work chair. Safety requirements.
NS-EN 1335-3
Office work chair. Safety test methods.
EN 60601-1
Medical electric equipment Part 1: General requirements for safety.
EN 60601-1-2
Medical electric equipment Part 1: General requirements for safety 1 Collateral
standard: Electromagnetic compatibility Requirements and test.
NS-EN 1021-1
Furniture Assessment of the ignitability of upholstered furniture part 1: Ignition
source: smouldering cigarette.
NS-EN 1021-2
Furniture Assessment of the ignitability of upholstered furniture part 1: Ignition
source: match flame equivalent.
93/42/EØF
marked. (Equipment class I)
NS-EN ISO 14971
Medical devices. Application of risk management to medical devices.

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