Coagulation factor II (prothrombin) mutation IVD, kit, nucleic acid technique (NAT) - UK MHRA Medical Device Registration

Coagulation factor II (prothrombin) mutation IVD, kit, nucleic acid technique (NAT) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 164951. The device is manufactured by Anatolia Tanı ve Biyoteknoloji Ürünleri Ar-Ge San. ve Tic. AŞ from Turkey, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Launch Diagnostics Limited.

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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In Vitro Diagnostic Device

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Coagulation factor II (prothrombin) mutation IVD, kit, nucleic acid technique (NAT)

MHRA Device ID: 164951•Ref: 164951

Device Type

In Vitro Diagnostic Device

Devices

Coagulation factor II (prothrombin) mutation IVD, kit, nucleic acid technique (NAT)

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Apr 5, 2024

Manufacturer Information

Name

Anatolia Tanı ve Biyoteknoloji Ürünleri Ar-Ge San. ve Tic. AŞ

Address

Hasanpasa Mah. Beydagi Sk No: 1-9 H

Istanbul, Sultanbeyli, Turkey

Created Date

Apr 28, 2021

Authorized Representative

Name

Launch Diagnostics Limited

Relationship Type

UK Responsible Person

Address

Unit 20 Ash Way Thorp Arch Estate

Wetherby, England, United Kingdom

Postcode: LS23 7FA

DJ Fang

MedTech Regulatory Expert

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Coagulation factor II (prothrombin) mutation IVD, kit, nucleic acid technique (NAT) - UK MHRA Medical Device Registration

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