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:

Rehabilitationsmittel GmbH Artlandstrasse 57-59

Quakenbrück

D-49610

Germany

Authorised Representative/ UK Responsible Person
Name: Medi-Plinth Equipment Limited
Address:

7-11 Holywells Road

Ipswich

IP3 0DL

United Kingdom

Code/Term Type

All-plastic conventional wheelchair All-plastic conventional wheelchair Class I

Freestanding patient lifting system electrically-powered Freestanding patient lifting system electrically-powered Class I

Freestanding patient lifting system electrically-powered Freestanding patient lifting system electrically-powered 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
All-plastic conventional wheelchair	All-plastic conventional wheelchair	Class I
Freestanding patient lifting system electrically-powered	Freestanding patient lifting system electrically-powered	Class I
Freestanding patient lifting system electrically-powered	Freestanding patient lifting system electrically-powered	Class I