SARS-CoV-2 antigen IVD, kit, fluorescent immunoassay - UK MHRA Medical Device Registration

SARS-CoV-2 antigen IVD, kit, fluorescent immunoassay is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 68884. 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.

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SARS-CoV-2 antigen IVD, kit, fluorescent immunoassay

MHRA Device ID: 68884•Ref: 68884

Device Type

In Vitro Diagnostic Device

Devices

SARS-CoV-2 antigen IVD, kit, fluorescent immunoassay

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, fluorescent immunoassay - UK MHRA Medical Device Registration

Device Type

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Date Registered

Last Updated

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Address

Created Date

Name

Relationship Type

Address

DJ Fang

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