Peripheral artery stent, bare-metal - UK MHRA Medical Device Registration

Peripheral artery stent, bare-metal is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 159183. The device is manufactured by Cordis Corporation from United States, classified as General Medical Device. The authorized representative in the UK is Cordis Medical UK Limited.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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General Medical Device

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Peripheral artery stent, bare-metal

MHRA Device ID: 159183•Ref: 159183

Device Type

General Medical Device

Devices

Peripheral artery stent, bare-metal

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Nov 11, 2023

Manufacturer Information

Name

Cordis Corporation

Address

14201 North West 60th Avenue

Miami Lakes, Florida, United States

Created Date

Oct 28, 2022

Authorized Representative

Name

Cordis Medical UK Limited

Relationship Type

UK Responsible Person

Address

Suite 402, Chadwick House Birchwood Park

Warrington, England, United Kingdom

Postcode: WA3 6AE

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Other Products from Cordis Corporation (10)

Other Products from Same Authorized Representative (10)

Peripheral artery stent, bare-metal - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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