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 84735. The device is manufactured by Humasis Co., Ltd. from South Korea, classified as In Vitro Diagnostic Device. The authorized representative in the UK is MT Promedt Consulting Ltd.

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

MHRA Device ID: 84735•Ref: 84735

Device Type

In Vitro Diagnostic Device

Devices

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

Type

IVD General

Date Registered

Jun 7, 2021

Last Updated

Oct 5, 2023

Manufacturer Information

Name

Humasis Co., Ltd.

Address

Rm.114, 502, 504, 604, 604-1, B03-01, B03-02, 88, Jeonpa-ro, Dongan-gu

Anyang-si, Gyeonggi-do, South Korea

Created Date

Jun 7, 2021

Authorized Representative

Name

MT Promedt Consulting Ltd

Relationship Type

UK Responsible Person

Address

Beaver House, 23-38 Hythe Bridge Street

Oxford, England, United Kingdom

Postcode: OX1 2EP

DJ Fang

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Registered: Jun 7, 2021

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

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