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 - Carnamedica Sp z o o

Address:

Ul. Olszynki Grochowskiej 21 lok. U6

Warsaw

04-281

Poland

Authorised Representative/ UK Responsible Person
Name: Bridge to Life (Europe) Ltd.
Address:

LU311 The Light Bulb 1 Filament Walk

Wandsworth

London

Greater London SW18 4GQ

England United Kingdom

Code/Term Type

Donor-organ perfusion catheter Donor-organ perfusion catheter Class IIa

Donor-organ/tissue/cell preservation solution Donor-organ/tissue/cell preservation solution Class III

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
Donor-organ perfusion catheter	Donor-organ perfusion catheter	Class IIa
Donor-organ/tissue/cell preservation solution	Donor-organ/tissue/cell preservation solution	Class III