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 - REBOTEC Rehabilitationsmittel GmbH

Address:

Artlandstr. 57-59

Quakenbrück

49610

Germany

Authorised Representative/ UK Responsible Person
Name: OMC MEDICAL Ltd
Address:

Planet House North Heath Lane

Horsham

West Sussex RH12 5QE

United Kingdom

Code/Term Type

Elbow crutch Elbow crutch Class I

Handgrip disability-assistive walker non-powered non-foldable Handgrip disability-assistive walker non-powered non-foldable 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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Code/Term		Type
Elbow crutch	Elbow crutch	Class I
Handgrip disability-assistive walker non-powered non-foldable	Handgrip disability-assistive walker non-powered non-foldable	Class I