United Kingdom MHRA device registration 79491

Cardiac/peripheral vascular guidewire, single-use

United Kingdom flagUnited Kingdom·General Medical Device·Brivant Limited T/A Lake Region Medical·Registered May 5, 2021
Registration details
Device ID
79491
Date Registered
May 5, 2021
Last Updated
Dec 22, 2022
Device classification
Device Type
General Medical Device
Devices
Cardiac/peripheral vascular guidewire, single-use
Type
Class III
Manufacturer
Address
Parkmore West Business Park
Galway, Ireland
Created Date
May 5, 2021
Authorized Representative
Relationship Type
UK Responsible Person
Address
Compass House, Vision Park Histon c/o Cr360 – UL International
Cambridge, England, United Kingdom
Postcode: CB24 9BZ
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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 79491. The device is manufactured by Brivant Limited T/A Lake Region Medical from Ireland, classified as General Medical Device. The authorized representative in the UK is Emergo Consulting (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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