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 - Cordis US Corp.

Address:

14201 North West 60th Avenue

Miami Lakes

Florida 33014

United States

Authorised Representative/ UK Responsible Person
Name: Cordis Medical UK Limited
Address:

Suite 402 Chadwick House Birchwood Park

Warrington

WA3 6AE

England United Kingdom

Code/Term Type

Bare-metal carotid artery stent Bare-metal carotid artery stent Class III

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

Endomyocardial biopsy forceps single-use Endomyocardial biopsy forceps single-use Class III

Peripheral angioplasty balloon catheter basic Peripheral angioplasty balloon catheter basic Class III

Peripheral angioplasty balloon catheter basic Peripheral angioplasty balloon catheter basic 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
Bare-metal carotid artery stent	Bare-metal carotid artery stent	Class III
Vascular guide-catheter single-use	Vascular guide-catheter single-use	Class III
Endomyocardial biopsy forceps single-use	Endomyocardial biopsy forceps single-use	Class III
Peripheral angioplasty balloon catheter basic	Peripheral angioplasty balloon catheter basic	Class III
Peripheral angioplasty balloon catheter basic	Peripheral angioplasty balloon catheter basic	Class III