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 - Intervascular SAS

Address:

ZI Athélia I 13705

CEDEX

LA CIOTAT

13705

France

Authorised Representative/ UK Responsible Person
Name: Getinge Ltd.
Address:

14-15 Burford Way Boldon Business Park

Boldon Colliery Tyne and Wear

Boldon

NE35 9PZ

England United Kingdom

Code/Term Type

Open-surgery blood vessel sizer single-use Open-surgery blood vessel sizer single-use Class IIa

Synthetic vascular graft Synthetic vascular graft Class III

Cardiovascular patch animal-derived Cardiovascular patch animal-derived 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
Open-surgery blood vessel sizer single-use	Open-surgery blood vessel sizer single-use	Class IIa
Synthetic vascular graft	Synthetic vascular graft	Class III
Cardiovascular patch animal-derived	Cardiovascular patch animal-derived	Class III