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 Dymind Biotechnology Co.Ltd.

Address:

10th Floor Building B High-tech Park GuangqiaoRoad Tianliao Community Yutang Street Guangming District Shenzhen 518107 P.R. China

Shenzhen

518107

China

Authorised Representative/ UK Responsible Person
Name: PureUKCA Ltd
Address:

59 St. Martin's Lane

London

Middlesex WC2N 4JS

England United Kingdom

Code/Term Type

C-reactive protein (CRP) IVD control C-reactive protein (CRP) IVD control IVD General

Serum amyloid A IVD kit nephelometry/turbidimetry Serum amyloid A IVD kit nephelometry/turbidimetry IVD General

Blood cell lysis reagent IVD Blood cell lysis reagent IVD 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
C-reactive protein (CRP) IVD control	C-reactive protein (CRP) IVD control	IVD General
Serum amyloid A IVD kit nephelometry/turbidimetry	Serum amyloid A IVD kit nephelometry/turbidimetry	IVD General
Blood cell lysis reagent IVD	Blood cell lysis reagent IVD	IVD General