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 - ResMed SAS

Address:

Parc Technologique de Lyon 292 Allee Jacques Monod

Saint Priest Cedex

69791

France

Authorised Representative/ UK Responsible Person
Name: ResMed (UK) Limited
Address:

Becquerel Avenue Quad 1 First Floor

Harwell Campus

Didcot

Oxfordshire OX11 0RA

England 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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