Percutaneous radio-frequency ablation probe, denervation, monopolar, single-use - UK MHRA Medical Device Registration
Percutaneous radio-frequency ablation probe, denervation, monopolar, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 191130. The device is manufactured by Medtronic Sofamor Danek 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
Percutaneous radio-frequency ablation probe, denervation, monopolar, single-use
Type
Class IIb
Date Registered
Nov 26, 2024
Last Updated
Dec 16, 2023
Address
1800 Pyramid Place
Memphis, TN, United States
Created Date
Mar 9, 2021
Relationship Type
Address
Building 9 Croxley Park
Watford, Herts, England, United Kingdom
Postcode: WD18 8WW
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