SARS-CoV-2/influenza A/B antigen IVD, kit, immunochromatographic test (ICT), rapid - UK MHRA Medical Device Registration

SARS-CoV-2/influenza A/B antigen IVD, kit, immunochromatographic test (ICT), rapid is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 134499. The device is manufactured by Kangmei Tianhong Biotech (Beijing) Co., Ltd. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Wellkang Ltd.

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SARS-CoV-2/influenza A/B antigen IVD, kit, immunochromatographic test (ICT), rapid

MHRA Device ID: 134499•Ref: 134499

Device Type

In Vitro Diagnostic Device

Devices

SARS-CoV-2/influenza A/B antigen IVD, kit, immunochromatographic test (ICT), rapid

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Oct 17, 2023

Manufacturer Information

Name

Kangmei Tianhong Biotech (Beijing) Co., Ltd.

Address

#16, No.1 Gaolizhang Road,

Haidian, Beijing, China

Created Date

Dec 16, 2021

Authorized Representative

Name

Wellkang Ltd

Relationship Type

Authorised Representative (Northern Ireland)

Address

Enterprise Hub, NW Business Complex 1 Beraghmore Road

Derry, Northern Ireland, Northern Ireland, United Kingdom

Postcode: BT48 8SE

DJ Fang

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Other Products from Kangmei Tianhong Biotech (Beijing) Co., Ltd. (6)

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SARS-CoV-2/influenza A/B antigen IVD, kit, immunochromatographic test (ICT), rapid - UK MHRA Medical Device Registration

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Created Date

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Address

DJ Fang

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