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 - Hubei MEIBAO Biotechnology Co. Ltd

Address:

No.5 Hongfu Road Shayang Economic Development Zone Jingmen City

Hubei Province

448200

China

Authorised Representative/ UK Responsible Person
Name: SUNGO Certification Company Limited
Address:

3rd Floor 70 Gracechurch Street

London

EC3V 0HR

England United Kingdom

Code/Term Type

Total human chorionic gonadotropin (HCG) IVD kit immunochromatographic test (ICT) rapid Total human chorionic gonadotropin (HCG) IVD kit immunochromatographic test (ICT) rapid IVD Devices for Self-Testing

Luteinizing hormone (LH) IVD kit rapid ICT clinical Luteinizing hormone (LH) IVD kit rapid ICT clinical IVD Devices for Self-Testing

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
Total human chorionic gonadotropin (HCG) IVD kit immunochromatographic test (ICT) rapid	Total human chorionic gonadotropin (HCG) IVD kit immunochromatographic test (ICT) rapid	IVD Devices for Self-Testing
Luteinizing hormone (LH) IVD kit rapid ICT clinical	Luteinizing hormone (LH) IVD kit rapid ICT clinical	IVD Devices for Self-Testing