Brain biopsy procedure kit - UK MHRA Medical Device Registration

Brain biopsy procedure kit is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 168855. 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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Brain biopsy procedure kit

MHRA Device ID: 168855•Ref: 168855

Device Type

General Medical Device

Devices

Brain biopsy procedure kit

Type

Class III

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

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Brain biopsy procedure kit - UK MHRA Medical Device Registration

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