Manual goniometer - UK MHRA Medical Device Registration
Manual goniometer is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 123392. The device is manufactured by Howmedica Osteonics 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.
Device Type
General Medical Device
Devices
Manual goniometer
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Dec 28, 2023
Address
325 Corporate Drive
Mahwah, New Jersey, United States
Created Date
Mar 26, 2021
Name
Stryker UK LtdRelationship Type
Address
Stryker House Hambridge Road
Newbury, Berkshire, England, United Kingdom
Postcode: RG14 5AW
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