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 130955. The device is manufactured by evonos GmbH & Co. KG from Germany, classified as General Medical Device. The authorized representative in the UK is MEDAGENT INTERNATIONAL 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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Automatic cranial perforator, single-use

MHRA Device ID: 130955•Ref: 130955

Device Type

General Medical Device

Devices

Automatic cranial perforator, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Jan 16, 2024

Manufacturer Information

Name

evonos GmbH & Co. KG

Address

Stockacher Str. 134

Tuttlingen, Baden-Wuerttemberg, Germany

Created Date

Jan 5, 2022

Authorized Representative

Name

MEDAGENT INTERNATIONAL UK LIMITED

Relationship Type

UK Responsible Person

Address

2 St Andrews Place

Lewes, East Sussex, England, United Kingdom

Postcode: BN7 1UP

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Other Products from evonos GmbH & Co. KG (10)

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

Device Type

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Type

Date Registered

Last Updated

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Address

Created Date

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Address

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