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 121232. The device is manufactured by Zimmer Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Zimmer Biomet 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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Shoulder glenoid fossa prosthesis, prefabricated

MHRA Device ID: 121232•Ref: 121232

Device Type

General Medical Device

Devices

Shoulder glenoid fossa prosthesis, prefabricated

Type

Class III

Date Registered

Nov 19, 2024

Last Updated

Apr 23, 2024

Manufacturer Information

Name

Zimmer Inc.

Address

1800 West Center Street

Indiana, Warsaw, United States

Created Date

Apr 30, 2021

Authorized Representative

Name

Zimmer Biomet UK Limited

Relationship Type

UK Responsible Person

Address

Stella Building Windmill Hill Business Park Whitehill Way

Swindon, England, United Kingdom

Postcode: SN5 6NX

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

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