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 - Biotech GmbH

Address:

Hagenauer Str. 17-19

Wiesbaden

65203

Germany

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

Langton Kennels DUNS

TD11 3QN

Langton Kennels

TD11 3QN

Scotland United Kingdom

Code/Term Type

Funnel chest remodelling bar Funnel chest remodelling bar Class IIb

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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