Abdominal hernia truss, reusable - UK MHRA Medical Device Registration
Abdominal hernia truss, reusable is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 122058. The device is manufactured by Tytex A/S from Denmark, classified as General Medical Device. The authorized representative in the UK is Qserve Group 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
Abdominal hernia truss, reusable
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Oct 31, 2024
Relationship Type
Address
49 Greek Street
London, England, United Kingdom
Postcode: W1D 4EG
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