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

Back to MHRA

Manufacturer's Devices - REBOTEC® Rehabilitationsmittel GmbH

Address:

Artlandstraße 57

Quakenbrück

49610

Germany

Authorised Representative/ UK Responsible Person
Name: Trulife
Address:

41 Amos Road

Sheffield

South Yorkshire S9 1BX

United Kingdom

Code/Term Type

Elbow crutch Elbow crutch 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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