United Kingdom MHRA device registration 182252

Peripheral vascular guidewire, manual

United Kingdom·General Medical Device·Covidien llc·Registered Nov 26, 2024

Registration details

Device ID: 182252
MHRA Reference Number: 182252
Date Registered: Nov 26, 2024
Last Updated: Aug 10, 2024

Device classification

Device Type: General Medical Device
Devices: Peripheral vascular guidewire, manual
Type: Class I

Manufacturer

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

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About this record

Peripheral vascular guidewire, manual is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 182252. 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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