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 136820. The device is manufactured by Tornier, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Stryker UK 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: 136820•Ref: 136820

Device Type

General Medical Device

Devices

Shoulder glenoid fossa prosthesis, prefabricated

Type

Class III

Date Registered

Apr 26, 2021

Last Updated

Oct 13, 2022

Manufacturer Information

Name

Tornier, Inc.

Address

10801 Nesbitt Avenue South

Bloomington, Minnesota, United States

Created Date

Apr 26, 2021

Authorized Representative

Name

Stryker UK Ltd

Relationship Type

UK Responsible Person

Address

Stryker House Hambridge Road

Newbury, Berkshire, England, United Kingdom

Postcode: RG14 5AW

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

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