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 71938. The device is manufactured by Abbott Medical from United States, classified as General Medical Device. The authorized representative in the UK is Abbott Medical UK 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, monopolar, single-use

MHRA Device ID: 71938•Ref: 71938

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

Jul 5, 2024

Manufacturer Information

Name

Abbott Medical

Address

5050 Nathan Lane North

Plymouth, Minnesota, United States

Created Date

Jan 15, 2021

Authorized Representative

Name

Abbott Medical UK Limited

Relationship Type

UK Responsible Person

Address

Elder House Central Boulevard Blythe Valley Business Park

Solihull, West Midlands, England, United Kingdom

Postcode: B90 8AJ

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Percutaneous radio-frequency ablation probe, denervation, monopolar, single-use - UK MHRA Medical Device Registration

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Date Registered

Last Updated

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Address

Created Date

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Address

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