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 68883. The device is manufactured by Diasia Biomedical Technology Co., Ltd. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is CMC Medical Devices 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: 68883•Ref: 68883

Device Type

In Vitro Diagnostic Device

Devices

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

Type

IVD General

Date Registered

Mar 8, 2021

Last Updated

Nov 9, 2022

Manufacturer Information

Name

Diasia Biomedical Technology Co., Ltd.

Address

3th B, 4th Floor, Building No.4, Chuangfu Industrial Park, Xixiang Tiegang Reservoir Road, Baoan District,

Shenzhen, China

Created Date

Mar 8, 2021

Authorized Representative

Name

CMC Medical Devices LTD

Relationship Type

UK Responsible Person

Address

Office 32 19-21 Crawford Street

London, United Kingdom

Postcode: W1H 1PJ

DJ Fang

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Other Products from Diasia Biomedical Technology Co., Ltd. (4)

Other Products from Same Authorized Representative (10)

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

Device Type

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Created Date

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Address

DJ Fang

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