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 - StethoMe Sp. z o.o.

Address:

ul. Winogrady 18a

Poznan

61-663

Poland

Authorised Representative/ UK Responsible Person
Name: Compliance Solutions (Lifesciences) Ltd
Address:

Suite 10 Dunswood House 1 Dunswood Road

Cumbernauld

Glasgow

G67 3EN

United Kingdom

Code/Term Type

Electronic stethoscope Electronic stethoscope Class IIa

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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