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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 79494. The device is manufactured by Brivant Limited T/A Lake Region Medical from Ireland, classified as Active implantable device (Directive 90/385/EEC only). 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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MHRA Registered
Active implantable device (Directive 90/385/EEC only)
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Cardiac/peripheral vascular guidewire, single-use
MHRA Device ID: 79494

Device Type

Active implantable device (Directive 90/385/EEC only)

Devices

Cardiac/peripheral vascular guidewire, single-use

Type

Active implantable Medical device

Date Registered

May 5, 2021

Last Updated

Dec 22, 2022

Manufacturer Information

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 โ€“ UL International

Cambridge, England, United Kingdom

Postcode: CB24 9BZ

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