Public Access Database for Medical Device Registration

Registration does not represent any form of accreditation, certification or approval by the UK Competent Authority(MHRA)
Where a conformity assessment certificate is listed as expired, existing products already placed on the market prior to the expiry may not be affected by this expiry and can continue to be used. This expiry stops new products being placed on the market until there is a new certificate of conformity

Manufacturer's By Name

By Device

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Manufacturer's Devices - BENOIT SYSTEMES SAS

Address:

7 rue du pont

Billy-les-Chanceaux

21450

France

Authorised Representative/ UK Responsible Person
Name: Recare Ltd
Address:

13 Hanborough business park Lodge Road

Long Hanborough

Long Hanborough

Oxfordshire OX29 8LJ

United Kingdom

Code/Term Type

Wheelchair electric-motor-driven propulsion system Wheelchair electric-motor-driven propulsion system Class I

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

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