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 79657. The device is manufactured by Beijing Unidiag Technology Inc. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is NPZ technology 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: 79657•Ref: 79657

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

Feb 9, 2024

Manufacturer Information

Name

Beijing Unidiag Technology Inc.

Address

Tower 10-208, No.09, Tianfu Ave, China Bio-medicine Industry Park, Daxing District

Beijing, China

Created Date

May 5, 2021

Authorized Representative

Name

NPZ technology Ltd

Relationship Type

UK Responsible Person

Address

Stirling House Cambridge Innovation Park, Denny End Road, Waterbeach

Cambridge, Cambridgeshire, United Kingdom

Postcode: CB25 9QE

DJ Fang

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

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