Automatic cranial perforator, single-use - UK MHRA Medical Device Registration

Automatic cranial perforator, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 148357. The device is manufactured by adeor medical AG from Germany, classified as General Medical Device. The authorized representative in the UK is Adveniunt Medical International Limited (trading as Quality First International).

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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Automatic cranial perforator, single-use

MHRA Device ID: 148357•Ref: 148357

Device Type

General Medical Device

Devices

Automatic cranial perforator, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Nov 7, 2023

Manufacturer Information

Name

adeor medical AG

Address

Martinshof 5

Valley, Germany

Created Date

May 24, 2022

Authorized Representative

Name

Adveniunt Medical International Limited (trading as Quality First International)

Relationship Type

UK Responsible Person

Address

1 Cooks Road Stratford

London, England, United Kingdom

Postcode: E15 2PW

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Automatic cranial perforator, single-use - UK MHRA Medical Device Registration

Device Type

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Date Registered

Last Updated

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Created Date

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Address

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