C-reactive protein (CRP) IVD, kit, nephelometry/turbidimetry - UK MHRA Medical Device Registration

C-reactive protein (CRP) IVD, kit, nephelometry/turbidimetry is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 122717. The device is manufactured by Shenzhen Dymind Biotechnology Co.Ltd. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is PureUKCA Ltd.

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C-reactive protein (CRP) IVD, kit, nephelometry/turbidimetry

MHRA Device ID: 122717•Ref: 122717

Device Type

In Vitro Diagnostic Device

Devices

C-reactive protein (CRP) IVD, kit, nephelometry/turbidimetry

Type

IVD General

Date Registered

Nov 10, 2021

Last Updated

Dec 22, 2022

Manufacturer Information

Name

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, China

Created Date

Nov 10, 2021

Authorized Representative

Name

PureUKCA Ltd

Relationship Type

UK Responsible Person

Address

59 St. Martin's Lane

London, Middlesex, England, United Kingdom

Postcode: WC2N 4JS

DJ Fang

MedTech Regulatory Expert

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C-reactive protein (CRP) IVD, kit, nephelometry/turbidimetry - UK MHRA Medical Device Registration

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