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.

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.

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Percutaneous radio-frequency ablation probe, denervation, bipolar

MHRA Device ID: 205625•Ref: 205625

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

Manufacturer Information

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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Percutaneous radio-frequency ablation probe, denervation, bipolar - UK MHRA Medical Device Registration

Device Type

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Created Date

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Address

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