Patella prosthesis trial - UK MHRA Medical Device Registration

Patella prosthesis trial is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 131825. The device is manufactured by Arthrex Inc from United States, classified as General Medical Device. The authorized representative in the UK is Emergo Consulting (UK) 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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Patella prosthesis trial

MHRA Device ID: 131825•Ref: 131825

Device Type

General Medical Device

Devices

Patella prosthesis trial

Type

Class IIa

Date Registered

Sep 22, 2021

Last Updated

Dec 22, 2022

Manufacturer Information

Name

Arthrex Inc

Address

1370 Creekside Blvd

Naples, Florida, United States

Created Date

Sep 22, 2021

Authorized Representative

Name

Emergo Consulting (UK) Limited

Relationship Type

UK Responsible Person

Address

Compass House, Vision Park Histon c/o Cr360 – UL International

Cambridge, England, United Kingdom

Postcode: CB24 9BZ

DJ Fang

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Other Products from Arthrex Inc (10)

Other Products from Same Authorized Representative (10)

Patella 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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