Shoulder glenoid fossa prosthesis, prefabricated - UK MHRA Medical Device Registration

Shoulder glenoid fossa prosthesis, prefabricated is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 67365. The device is manufactured by Depuy Orthopaedics, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Johnson & Johnson 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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Shoulder glenoid fossa prosthesis, prefabricated

MHRA Device ID: 67365•Ref: 67365

Device Type

General Medical Device

Devices

Shoulder glenoid fossa prosthesis, prefabricated

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Jul 9, 2024

Manufacturer Information

Name

Depuy Orthopaedics, Inc.

Address

700 Orthopaedic Drive

warsaw, United States

Created Date

Feb 22, 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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Shoulder glenoid fossa prosthesis, prefabricated - UK MHRA Medical Device Registration

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Date Registered

Last Updated

Name

Address

Created Date

Name

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Address

DJ Fang

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