Percutaneous radio-frequency ablation system generator - UK MHRA Medical Device Registration

Percutaneous radio-frequency ablation system generator is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 68612. The device is manufactured by Smith & Nephew, Inc., Endoscopy Division from United States, classified as General Medical Device. The authorized representative in the UK is T.J.Smith and Nephew,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 system generator

MHRA Device ID: 68612•Ref: 68612

Device Type

General Medical Device

Devices

Percutaneous radio-frequency ablation system generator

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Jan 20, 2024

Manufacturer Information

Name

Smith & Nephew, Inc., Endoscopy Division

Address

150 Minuteman Road

Andover, Massachusetts, United States

Created Date

Mar 5, 2021

Authorized Representative

Name

T.J.Smith and Nephew,Limited

Relationship Type

UK Responsible Person

Address

101 Hessle Road

Hull, England, United Kingdom

Postcode: HU3 2BN

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Percutaneous radio-frequency ablation system generator - UK MHRA Medical Device Registration

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DJ Fang

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