Cardiac/peripheral vascular guidewire, single-use - UK MHRA Medical Device Registration

Cardiac/peripheral vascular guidewire, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 159188. 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.

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Cardiac/peripheral vascular guidewire, single-use

MHRA Device ID: 159188•Ref: 159188

Device Type

General Medical Device

Devices

Cardiac/peripheral vascular guidewire, single-use

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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Other Products from Same Authorized Representative (10)

Cardiac/peripheral vascular guidewire, single-use - UK MHRA Medical Device Registration

Device Type

Devices

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Date Registered

Last Updated

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Address

Created Date

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Address

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