Automatic cranial perforator, reusable - UK MHRA Medical Device Registration

Automatic cranial perforator, reusable is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 95618. 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.

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Automatic cranial perforator, reusable

MHRA Device ID: 95618•Ref: 95618

Device Type

General Medical Device

Devices

Automatic cranial perforator, reusable

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Sep 5, 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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Automatic cranial perforator, reusable - UK MHRA Medical Device Registration

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