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 - SomnoMed AG

Address:

Steinhauserstrasse 74

Zug

6300

Switzerland

Authorised Representative/ UK Responsible Person
Name: SOMNOMED UK LIMITED
Address:

Raleigh House 14c Compass Point Business Park Stocks Bridge Way

St. Ives

Huntingdonshire PE27 5JL

England United Kingdom

Code/Term Type

Mandible-repositioning sleep-disordered breathing orthosis Mandible-repositioning sleep-disordered breathing orthosis Class I

Denture cleanser Denture cleanser Class I

Bite registration rim Bite registration rim Class I

Dental occlusal splint custom-made Dental occlusal splint custom-made

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
Mandible-repositioning sleep-disordered breathing orthosis	Mandible-repositioning sleep-disordered breathing orthosis	Class I
Denture cleanser	Denture cleanser	Class I
Bite registration rim	Bite registration rim	Class I
Dental occlusal splint custom-made	Dental occlusal splint custom-made