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Arthroplasty force sensor - UK MHRA Medical Device Registration

Arthroplasty force sensor is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 168000. The device is manufactured by Orthosensor, Inc. 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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General Medical Device
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Arthroplasty force sensor
MHRA Device ID: 168000โ€ขRef: 168000

Device Type

General Medical Device

Devices

Arthroplasty force sensor

Type

Class IIa

Last Updated

Oct 7, 2023

Manufacturer Information

Address

1855 Griffin Road Dania Beach

Florida, Florida, United States

Created Date

Mar 8, 2023

Authorized Representative

Relationship Type

UK Responsible Person

Address

Stryker House Hambridge Road

Newbury, Berkshire, England, United Kingdom

Postcode: RG14 5AW

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