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 183838. The device is manufactured by SYNTHES GMBH from Switzerland, classified as General Medical Device. The authorized representative in the UK is Johnson & Johnson Medical Ltd.

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Automatic cranial perforator, reusable

MHRA Device ID: 183838•Ref: 183838

Device Type

General Medical Device

Devices

Automatic cranial perforator, reusable

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Aug 10, 2024

Manufacturer Information

Name

SYNTHES GMBH

Address

EIMATTSTRASSE 3

4436 OBERDORF, Switzerland

Created Date

Feb 21, 2021

Authorized Representative

Name

Johnson & Johnson Medical Ltd

Relationship Type

UK Responsible Person

Address

Baird House 4 Lower Gilmore Bank

Edinburgh, Scotland, United Kingdom

Postcode: EH3 9QP

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Automatic cranial perforator, reusable - UK MHRA Medical Device Registration

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