United Kingdom MHRA device registration 205626

Percutaneous radio-frequency ablation probe, denervation, bipolar

United Kingdom·General Medical Device·Boston Scientific Neuromodulation Corporation·Registered Nov 26, 2024

Registration details

Device ID: 205626
MHRA Reference Number: 205626
Date Registered: Nov 26, 2024
Last Updated: Oct 18, 2024

Device classification

Device Type: General Medical Device
Devices: Percutaneous radio-frequency ablation probe, denervation, bipolar
Type: Class IIb

Manufacturer

Name: Boston Scientific Neuromodulation Corporation
Address: 25155 Rye Canyon Loop
Valencia, California, United States
Created Date: Apr 1, 2021

Authorized Representative

Name: Boston Scientific Limited
Relationship Type: UK Responsible Person
Address: Breakspear Park Breakspear Way
Hemel Hempstead, Hertfordshire, England, United Kingdom
Postcode: HP2 4TZ

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About this record

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 205626. 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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