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.

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In Vitro Diagnostic Device

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Influenza A/B virus antigen IVD, kit, rapid ICT, clinical

MHRA Device ID: 152393•Ref: 152393

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

Manufacturer Information

Name

Tianjin Bioscience Diagnostic Technology Co., Ltd.

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

Authorized Representative

Name

SUNGO Certification Company Limited

Relationship Type

UK Responsible Person

Address

3rd Floor, 70 Gracechurch Street

London, England, United Kingdom

Postcode: EC3V 0HR

DJ Fang

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Influenza A/B virus antigen IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

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