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 - Respiri Ltd.

Address:

Suite 1 Level 9

432 St. Kilda Road

Melbourne

Victoria 3004

Australia

Authorised Representative/ UK Responsible Person
Name: European Device Solutions Ltd
Address:

15 COANWOOD DRIVE Whitley Bay

WHITLEY BAY

TYNE AND WEAR NE25 9GB

England United Kingdom

Code/Term Type

Electronic stethoscope Electronic stethoscope 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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