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 - YD Diagnostics CORP.

Address:

76 Seori-Ro Idong-eup

Cheoin-Gu Yongin-Si

Gyeonggi-Do

17127

South Korea

Authorised Representative/ UK Responsible Person
Name: Chirus Limited
Address:

Greenhill House 26 Greenhill Crescent

Watford Business Park

Watford

Hertfordshire WD18 8JA

England United Kingdom

Code/Term Type

Urine analyser IVD point-of-care Urine analyser IVD point-of-care IVD General

Multiple urine analyte IVD control Multiple urine analyte IVD control IVD General

Multiple urine analyte IVD kit rapid colorimetric clinical Multiple urine analyte IVD kit rapid colorimetric 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
Urine analyser IVD point-of-care	Urine analyser IVD point-of-care	IVD General
Multiple urine analyte IVD control	Multiple urine analyte IVD control	IVD General
Multiple urine analyte IVD kit rapid colorimetric clinical	Multiple urine analyte IVD kit rapid colorimetric clinical	IVD General