Percutaneous radio-frequency ablation probe, denervation, bipolar - UK MHRA Medical Device Registration
Percutaneous radio-frequency ablation probe, denervation, bipolar is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 205625. The device is manufactured by Boston Scientific Neuromodulation Corporation from United States, classified as General Medical Device. The authorized representative in the UK is Boston Scientific Limited.
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Device Type
General Medical Device
Devices
Percutaneous radio-frequency ablation probe, denervation, bipolar
Type
Class IIb
Date Registered
Nov 26, 2024
Last Updated
Oct 18, 2024
Address
25155 Rye Canyon Loop
Valencia, California, United States
Created Date
Apr 1, 2021
Relationship Type
Address
Breakspear Park Breakspear Way
Hemel Hempstead, Hertfordshire, England, United Kingdom
Postcode: HP2 4TZ
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Percutaneous radio-frequency ablation probe, denervation, bipolar
Type: General Medical Device
Registered: Nov 26, 2024
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Registered: Nov 26, 2024
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