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 - P+F Products + Features GmbH

Address:

Argelsrieder Feld 1a

Weßling

Starnberg

Oberbayern 82234

Germany

Authorised Representative/ UK Responsible Person
Name: Jump Start Consulting Limited
Address:

Unit 24 Cranfield Innovation Centre

University Way

Cranfield

Bedfordshire MK43 0BT

England United Kingdom

Code/Term Type

Bicaval valve bioprosthesis Bicaval valve bioprosthesis 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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