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 73664. The device is manufactured by AGA Medical Corporation from United States, classified as General Medical Device. The authorized representative in the UK is Abbott Medical 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.
Device Type
General Medical Device
Devices
Cardiac/peripheral vascular guidewire, single-use
Type
Class III
Date Registered
Nov 26, 2024
Last Updated
Jul 5, 2024
Address
5050 Nathan Lane North
Plymouth, Minnesota, United States
Created Date
Feb 18, 2021
Relationship Type
Address
Elder House Central Boulevard Blythe Valley Business Park
Solihull, West Midlands, England, United Kingdom
Postcode: B90 8AJ
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