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 79484. The device is manufactured by Lake Region Medical Ltd. 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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Cardiac/peripheral vascular guidewire, single-use

MHRA Device ID: 79484•Ref: 79484

Device Type

General Medical Device

Devices

Cardiac/peripheral vascular guidewire, single-use

Type

Class III

Date Registered

Sep 24, 2024

Last Updated

May 2, 2024

Manufacturer Information

Name

Lake Region Medical Ltd.

Address

Butlersland

New Ross, Co. Wexford, Ireland

Created Date

May 4, 2021

Authorized Representative

Name

Emergo Consulting (UK) Limited

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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Other Products from Lake Region Medical Ltd. (2)

Peripheral vascular guidewire, manual

Type: General Medical Device

Registered: Nov 26, 2024

Peripheral vascular guidewire, manual

Type: General Medical Device

Registered: Nov 26, 2024

Other Products from Same Authorized Representative (10)

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

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