Embolic protection filtering guidewire - UK MHRA Medical Device Registration

Embolic protection filtering guidewire is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 159182. 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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Embolic protection filtering guidewire

MHRA Device ID: 159182•Ref: 159182

Device Type

General Medical Device

Devices

Embolic protection filtering guidewire

Type

Class III

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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Embolic protection filtering guidewire - UK MHRA Medical Device Registration

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