Peripheral vascular guidewire, manual - UK MHRA Medical Device Registration

Peripheral vascular guidewire, manual is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 182251. The device is manufactured by Covidien llc from United States, classified as General Medical Device. The authorized representative in the UK is Medtronic 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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Peripheral vascular guidewire, manual

MHRA Device ID: 182251•Ref: 182251

Device Type

General Medical Device

Devices

Peripheral vascular guidewire, manual

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Aug 10, 2024

Manufacturer Information

Name

Covidien llc

Address

4600 Nathan Lane North

Plymouth, Minnesota, United States

Created Date

Oct 17, 2023

Authorized Representative

Name

Medtronic Limited

Relationship Type

UK Responsible Person

Address

Building 9 Croxley Park

Watford, Herts, England, United Kingdom

Postcode: WD18 8WW

DJ Fang

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Peripheral vascular guidewire, manual - UK MHRA Medical Device Registration

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