Knee arthroplasty force sensor balance kit - UK MHRA Medical Device Registration

Knee arthroplasty force sensor balance kit is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 131829. 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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Knee arthroplasty force sensor balance kit

MHRA Device ID: 131829•Ref: 131829

Device Type

General Medical Device

Devices

Knee arthroplasty force sensor balance kit

Type

Class I

Date Registered

Sep 22, 2021

Last Updated

Jun 30, 2023

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

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Knee arthroplasty force sensor balance kit - UK MHRA Medical Device Registration

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DJ Fang

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