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 - Shenzhen Huaree Technology Co. Ltd

Address:

101 201 No. 17 Shouli Road Central Community Pingdi Street Longgang District Shenzhen

Guangdong Province

518117

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

Oral/upper respiratory tract specimen collection swab Oral/upper respiratory tract specimen collection swab Class I

General specimen collection kit IVD clinical General specimen collection kit IVD 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
Oral/upper respiratory tract specimen collection swab	Oral/upper respiratory tract specimen collection swab	Class I
General specimen collection kit IVD clinical	General specimen collection kit IVD clinical	IVD General