Glenoid orthopaedic reamer - UK MHRA Medical Device Registration

Glenoid orthopaedic reamer is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 99912. The device is manufactured by Stryker GmbH from Switzerland, 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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Glenoid orthopaedic reamer

MHRA Device ID: 99912•Ref: 99912

Device Type

General Medical Device

Devices

Glenoid orthopaedic reamer

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Jan 4, 2024

Manufacturer Information

Name

Stryker GmbH

Address

Bohnackerweg, 1

Selzach, Switzerland

Created Date

Mar 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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Glenoid orthopaedic reamer - UK MHRA Medical Device Registration

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Address

Created Date

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DJ Fang

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