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 - HAIMEN SHENGBANG LABORATORY EQUIPMENT CO. LTD

Address:

No.126 Group 9 Zhangbei Village Haimen

Jiangsu Province

226110

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

General specimen collection kit IVD clinical General specimen collection kit IVD clinical IVD General

Urine specimen collection kit IVD Urine specimen collection kit IVD IVD General

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

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