SARS-CoV-2 antigen IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

SARS-CoV-2 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 158836. The device is manufactured by Beijing Jinwofu Bioengineering Technology Co.,Ltd. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is lotus global co ltd.

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.

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SARS-CoV-2 antigen IVD, kit, rapid ICT, clinical

MHRA Device ID: 158836•Ref: 158836

Device Type

In Vitro Diagnostic Device

Devices

SARS-CoV-2 antigen IVD, kit, rapid ICT, clinical

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Jan 16, 2024

Manufacturer Information

Name

Beijing Jinwofu Bioengineering Technology Co.,Ltd.

Address

Room 206, 1st Building, No.26, Jinyuan Road, Daxing District

Beijing, China

Created Date

Oct 23, 2022

Authorized Representative

Name

lotus global co ltd

Relationship Type

UK Responsible Person

Address

23 Maine Street

Reading, Reading, England, United Kingdom

Postcode: RG2 6AG

DJ Fang

MedTech Regulatory Expert

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SARS-CoV-2 antigen IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

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Date Registered

Last Updated

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Created Date

Name

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Address

DJ Fang

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