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 90233. The device is manufactured by Smith & Nephew Orthopaedics AG from Switzerland, classified as General Medical Device. The authorized representative in the UK is T.J.Smith and Nephew,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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Femoral stem prosthesis trial

MHRA Device ID: 90233•Ref: 90233

Device Type

General Medical Device

Devices

Femoral stem prosthesis trial

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Feb 10, 2024

Manufacturer Information

Name

Smith & Nephew Orthopaedics AG

Address

Oberneuhofstrasse 10d

Baar, Switzerland

Created Date

Feb 26, 2021

Authorized Representative

Name

T.J.Smith and Nephew,Limited

Relationship Type

UK Responsible Person

Address

101 Hessle Road

Hull, England, United Kingdom

Postcode: HU3 2BN

DJ Fang

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Other Products from Smith & Nephew Orthopaedics AG (10)

Other Products from Same Authorized Representative (10)

Femoral stem prosthesis trial - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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