Influenza A/B virus antigen IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration
Influenza A/B virus 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 152393. The device is manufactured by Tianjin Bioscience Diagnostic Technology Co., Ltd. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is SUNGO Certification Company 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.
Device Type
In Vitro Diagnostic Device
Devices
Influenza A/B virus antigen IVD, kit, rapid ICT, clinical
Type
IVD General
Date Registered
Nov 26, 2024
Last Updated
Oct 8, 2023
Address
Building 14, INT Medical Device Industrial Park, No. 16 Wujing Road, Dongli Economic and T&D Zone
Tianjin, China
Created Date
Jul 20, 2022
Relationship Type
Address
3rd Floor, 70 Gracechurch Street
London, England, United Kingdom
Postcode: EC3V 0HR
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