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 - MaRhyThe Systems GmbH & Co. KG

Address:

Industriestr 29

Grobenzell

82194

Germany

Authorised Representative/ UK Responsible Person
Name: Matrix Rhythm Therapy UK Ltd
Address:

5 Beswicks Road

Northwich

Cheshire CW8 1AP

England United Kingdom

Code/Term Type

Circulatory/musculoskeletal vibration therapy unit hand-held Circulatory/musculoskeletal vibration therapy unit hand-held Class IIa

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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