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 - Vivostat A/S

Address:

Vivostat A/S Borupvang 2

Lillerød

3450

Denmark

Authorised Representative/ UK Responsible Person
Name: Pegamento Ltd
Address:

Th'Owd Woolpack 42 Woods Lane

Dobcross

Oldham

Lancashire OL3 5AN

England United Kingdom

Code/Term Type

Platelet rich fibrin biochemical preparation/application kit endoscopic Platelet rich fibrin biochemical preparation/application kit endoscopic Class IIa

Platelet rich fibrin biochemical preparation/application kit endoscopic Platelet rich fibrin biochemical preparation/application kit endoscopic Class IIa

Platelet rich fibrin biochemical preparation/application kit endoscopic Platelet rich fibrin biochemical preparation/application kit endoscopic 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
Platelet rich fibrin biochemical preparation/application kit endoscopic	Platelet rich fibrin biochemical preparation/application kit endoscopic	Class IIa
Platelet rich fibrin biochemical preparation/application kit endoscopic	Platelet rich fibrin biochemical preparation/application kit endoscopic	Class IIa
Platelet rich fibrin biochemical preparation/application kit endoscopic	Platelet rich fibrin biochemical preparation/application kit endoscopic	Class III