Knee femur prosthesis trial, reusable - UK MHRA Medical Device Registration

Knee femur prosthesis trial, reusable is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 150665. The device is manufactured by Howmedica Osteonics Corp. 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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Knee femur prosthesis trial, reusable

MHRA Device ID: 150665•Ref: 150665

Device Type

General Medical Device

Devices

Knee femur prosthesis trial, reusable

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Dec 28, 2023

Manufacturer Information

Name

Howmedica Osteonics Corp.

Address

325 Corporate Drive

Mahwah, New Jersey, United States

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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Other Products from Howmedica Osteonics Corp. (10)

Other Products from Same Authorized Representative (10)

Knee femur prosthesis trial, reusable - UK MHRA Medical Device Registration

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Date Registered

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Address

Created Date

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