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.

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Polyolefin/fluoropolymer suture, monofilament

MHRA Device ID: 91953•Ref: 91953

Device Type

General Medical Device

Devices

Polyolefin/fluoropolymer suture, monofilament

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Jul 20, 2024

Manufacturer Information

Name

Betatech Medikal Cih. San. Mum. Ic ve Dis Tic. Ltd. Sti

Address

Ikitelli OSB.Ataturk Oto San. Sit.Unal Is Merkezi, 22.Sk. No:9 Basaksehir

Istanbul, Turkey

Created Date

Aug 3, 2021

Authorized Representative

Name

CMC Medical Devices LTD

Relationship Type

UK Responsible Person

Address

Office 32 19-21 Crawford Street

London, United Kingdom

Postcode: W1H 1PJ

DJ Fang

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Other Products from Betatech Medikal Cih. San. Mum. Ic ve Dis Tic. Ltd. Sti (10)

Other Products from Same Authorized Representative (10)

Polyolefin/fluoropolymer suture, monofilament - UK MHRA Medical Device Registration

Device Type

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Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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