HIV1/HIV2 antigen/antibody IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

HIV1/HIV2 antigen/antibody IVD, kit, rapid ICT, clinical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 148747. The device is manufactured by TURKLAB TIBBI MAL.SAN.VE TIC.A.S. from Turkey, classified as In Vitro Diagnostic Device. The authorized representative in the UK is E&E MEDICAL SUPPLIES LTD..

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In Vitro Diagnostic Device

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HIV1/HIV2 antigen/antibody IVD, kit, rapid ICT, clinical

MHRA Device ID: 148747•Ref: 148747

Device Type

In Vitro Diagnostic Device

Devices

HIV1/HIV2 antigen/antibody IVD, kit, rapid ICT, clinical

Type

IVD Annex II List A

Date Registered

Nov 26, 2024

Last Updated

Sep 3, 2024

Manufacturer Information

Name

TURKLAB TIBBI MAL.SAN.VE TIC.A.S.

Address

ITOB 10017 Sokak NO:2 Tekeli Menderes

Izmir, Turkey

Created Date

May 30, 2022

Authorized Representative

Name

E&E MEDICAL SUPPLIES LTD.

Relationship Type

UK Responsible Person

Address

Unit 2 Fairway Business Centre Westergate Road

Brighton, Sussex, England, United Kingdom

Postcode: BN2 4JZ

DJ Fang

MedTech Regulatory Expert

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HIV1/HIV2 antigen/antibody IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

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