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 160523. The device is manufactured by Cordis Cashel from Ireland, 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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Peripheral artery stent, bare-metal

MHRA Device ID: 160523•Ref: 160523

Device Type

General Medical Device

Devices

Peripheral artery stent, bare-metal

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Nov 10, 2023

Manufacturer Information

Name

Cordis Cashel

Address

Cahir Road

Cashel, Co. Tipperary, Ireland

Created Date

Nov 14, 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 Same Authorized Representative (10)

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

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Date Registered

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