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 - Tomed GmbH

Address:

Im Rapsfeld 57

Koln

50933

Germany

Authorised Representative/ UK Responsible Person
Name: PMF Consultants Ltd
Address:

10 Vail

Donaghadee

Co Down BT21 0QL

Northern Ireland United Kingdom

Code/Term Type

Mandible-repositioning sleep-disordered breathing orthosis Mandible-repositioning sleep-disordered breathing orthosis 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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