Public Access Database for Medical Device Registration

Registration does not represent any form of accreditation, certification or approval by the UK Competent Authority(MHRA)
Where a conformity assessment certificate is listed as expired, existing products already placed on the market prior to the expiry may not be affected by this expiry and can continue to be used. This expiry stops new products being placed on the market until there is a new certificate of conformity

Manufacturer's By Name

By Device

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Manufacturer's Devices - Humasis Co. Ltd.

Address:

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

Anyang-si

Gyeonggi-do 14042

South Korea

Authorised Representative/ UK Responsible Person
Name: MT Promedt Consulting Ltd
Address:

Beaver House 23-38 Hythe Bridge Street

Oxford

OX1 2EP

England United Kingdom

Code/Term Type

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

Multiple Plasmodium species antigen IVD kit rapid ICT clinical Multiple Plasmodium species antigen IVD kit rapid ICT clinical IVD General

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

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Code/Term		Type
SARS-CoV-2 antigen IVD kit rapid ICT clinical	SARS-CoV-2 antigen IVD kit rapid ICT clinical	IVD General
Multiple Plasmodium species antigen IVD kit rapid ICT clinical	Multiple Plasmodium species antigen IVD kit rapid ICT clinical	IVD General