United Kingdom MHRA device registration 148749

Hepatitis B virus surface antigen IVD, kit, rapid ICT, clinical

United Kingdom flagUnited Kingdom·In Vitro Diagnostic Device·TURKLAB TIBBI MAL.SAN.VE TIC.A.S.·Registered Nov 26, 2024
Registration details
Device ID
148749
MHRA Reference Number
148749
Date Registered
Nov 26, 2024
Last Updated
Sep 3, 2024
Device classification
Device Type
In Vitro Diagnostic Device
Devices
Hepatitis B virus surface antigen IVD, kit, rapid ICT, clinical
Type
IVD Annex II List A
Manufacturer
Address
ITOB 10017 Sokak NO:2 Tekeli Menderes
Izmir, Turkey
Created Date
May 30, 2022
Authorized Representative
Relationship Type
UK Responsible Person
Address
Unit 2 Fairway Business Centre Westergate Road
Brighton, Sussex, England, United Kingdom
Postcode: BN2 4JZ
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About this record

Hepatitis B virus surface antigen IVD, kit, rapid ICT, clinical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 148749. 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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