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 - Ectosense nv

Address:

Bosbessenlaan 19A

Rotselaar

Vlaams-Brabant 3110

Belgium

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

Sleep disorder interpretive software professional-only Sleep disorder interpretive software professional-only Class IIa

Wearable multiple physiological parameter recorder reusable Wearable multiple physiological parameter recorder reusable 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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Code/Term		Type
Sleep disorder interpretive software professional-only	Sleep disorder interpretive software professional-only	Class IIa
Wearable multiple physiological parameter recorder reusable	Wearable multiple physiological parameter recorder reusable	Class I