Aorta punch, single-use - UK MHRA Medical Device Registration
Aorta punch, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 86892. The device is manufactured by Medtronic, Inc 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.
Device Type
General Medical Device
Devices
Aorta punch, single-use
Type
Class IIa
Date Registered
Nov 26, 2024
Last Updated
Dec 16, 2023
Name
Medtronic, IncAddress
710 Medtronic Parkway
Minneapolis, MN, United States
Created Date
Feb 2, 2021
Relationship Type
Address
Building 9 Croxley Park
Watford, Herts, England, United Kingdom
Postcode: WD18 8WW
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