United Kingdom MHRA device registration 159189

Cardiac/peripheral vascular guidewire, single-use

United Kingdom·General Medical Device·Cordis Corporation·Registered Nov 26, 2024

Registration details

Device ID: 159189
MHRA Reference Number: 159189
Date Registered: Nov 26, 2024
Last Updated: Nov 11, 2023

Device classification

Device Type: General Medical Device
Devices: Cardiac/peripheral vascular guidewire, single-use
Type: Class IIa

Manufacturer

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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About this record

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 159189. 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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