Dura mater biomatrix implant - UK MHRA Medical Device Registration

Dura mater biomatrix implant is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 71799. The device is manufactured by Aesculap AG from Germany, classified as General Medical Device. The authorized representative in the UK is B. Braun Medical 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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Dura mater biomatrix implant

MHRA Device ID: 71799•Ref: 71799

Device Type

General Medical Device

Devices

Dura mater biomatrix implant

Type

Class III

Date Registered

Sep 8, 2024

Last Updated

Jul 18, 2024

Manufacturer Information

Name

Aesculap AG

Address

Am Aesculap Platz

Tuttlingen, Germany

Created Date

Mar 26, 2021

Authorized Representative

Name

B. Braun Medical Ltd

Relationship Type

UK Responsible Person

Address

Brookdale Road Chapeltown

Sheffield, South Yorkshire, United Kingdom

Postcode: S35 2PW

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Other Products from Aesculap AG (10)

Other Products from Same Authorized Representative (10)

Dura mater biomatrix implant - UK MHRA Medical Device Registration

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Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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