Hip/knee/ankle/foot orthosis - UK MHRA Medical Device Registration
Hip/knee/ankle/foot orthosis is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 129570. The device is manufactured by OPPO Medical Inc. from United States, classified as General Medical Device. The authorized representative in the UK is MT Promedt Consulting 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
Hip/knee/ankle/foot orthosis
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Oct 25, 2024
Address
Seattle City Centre, 1420 Fifth Ave., Ste. 220080
Seattle, Washington, United States
Created Date
Dec 30, 2021
Relationship Type
Address
Beaver House, 23-38 Hythe Bridge Street
Oxford, England, United Kingdom
Postcode: OX1 2EP
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