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

Percutaneous radio-frequency ablation probe cannula, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 74350. The device is manufactured by PAJUNK GmbH Medizintechnologie from Germany, classified as General Medical Device. The authorized representative in the UK is Pajunk UK Medical Products Ltd.

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 cannula, single-use

MHRA Device ID: 74350•Ref: 74350

Device Type

General Medical Device

Devices

Percutaneous radio-frequency ablation probe cannula, single-use

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Dec 20, 2023

Manufacturer Information

Name

PAJUNK GmbH Medizintechnologie

Address

Karl-Hall-Str. 1 Karl-Hall-Str. 1

Geisingen, Baden-Wuerttemberg, Germany

Created Date

Mar 15, 2021

Authorized Representative

Name

Pajunk UK Medical Products Ltd

Relationship Type

UK Responsible Person

Address

Harlands Accountants Llp The Greenhouse Amos Drive Greencroft Industrial Park Annfield Plain

Stanley, County Durham, England, United Kingdom

Postcode: DH9 7XN

DJ Fang

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Other Products from PAJUNK GmbH Medizintechnologie (10)

Other Products from Same Authorized Representative (10)

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

Device Type

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Date Registered

Last Updated

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Address

Created Date

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Relationship Type

Address

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