Polyolefin/fluoropolymer suture, monofilament - UK MHRA Medical Device Registration
Polyolefin/fluoropolymer suture, monofilament is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 91953. The device is manufactured by Betatech Medikal Cih. San. Mum. Ic ve Dis Tic. Ltd. Sti from Turkey, classified as General Medical Device. The authorized representative in the UK is CMC Medical Devices 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
Polyolefin/fluoropolymer suture, monofilament
Type
Class III
Date Registered
Nov 26, 2024
Last Updated
Jul 20, 2024
Address
Ikitelli OSB.Ataturk Oto San. Sit.Unal Is Merkezi, 22.Sk. No:9 Basaksehir
Istanbul, Turkey
Created Date
Aug 3, 2021
Relationship Type
Address
Office 32 19-21 Crawford Street
London, United Kingdom
Postcode: W1H 1PJ
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