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 - ResApp Health Limited

Address:

Level 12 100 Creek Street

Brisbane

Queensland 4000

Australia

Authorised Representative/ UK Responsible Person
Name: MT Promedt Consulting Ltd
Address:

Beaver House 23-38 Hythe Bridge Street

Oxford

OX1 2EP

England United Kingdom

Code/Term Type

Respiratory sound analysis software professional-only Respiratory sound analysis software professional-only Class IIa

Sleep disorder interpretive software patient-use Sleep disorder interpretive software patient-use Class I

Cough ambulatory recording system Cough ambulatory recording system 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
Respiratory sound analysis software professional-only	Respiratory sound analysis software professional-only	Class IIa
Sleep disorder interpretive software patient-use	Sleep disorder interpretive software patient-use	Class I
Cough ambulatory recording system	Cough ambulatory recording system	Class I