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 - PendraCare International BV

Address:

Van der Waalspark 22

Van der Waalspark 22

Leek

9351VC

Netherlands

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

Pure Offices Plato Close

Warwick

CV34 6WE

England United Kingdom

Code/Term Type

Vascular guide-catheter single-use Vascular guide-catheter single-use Class III

Angiographic catheter single-use Angiographic catheter single-use Conformity Assessment Certificate Expired Class III

Angiographic catheter single-use Angiographic catheter single-use 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
Vascular guide-catheter single-use	Vascular guide-catheter single-use	Class III
Angiographic catheter single-use	Angiographic catheter single-use Conformity Assessment Certificate Expired	Class III
Angiographic catheter single-use	Angiographic catheter single-use	Class III