Femoral stem prosthesis trial - UK MHRA Medical Device Registration

Femoral stem prosthesis trial is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 99263. The device is manufactured by MAKO Surgical 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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Femoral stem prosthesis trial

MHRA Device ID: 99263•Ref: 99263

Device Type

General Medical Device

Devices

Femoral stem prosthesis trial

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Dec 5, 2023

Manufacturer Information

Name

MAKO Surgical Corp

Address

3365 Enterprise Avenue

Weston, Florida, United States

Created Date

Mar 2, 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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Femoral stem prosthesis trial - UK MHRA Medical Device Registration

Device Type

Devices

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Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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