United Kingdom MHRA device registration 175369

Serum amyloid A IVD, kit, nephelometry/turbidimetry

United Kingdom·In Vitro Diagnostic Device·Shenzhen Dymind Biotechnology Co.Ltd.·Registered Sep 29, 2024

Registration details

Device ID: 175369
MHRA Reference Number: 175369
Date Registered: Sep 29, 2024
Last Updated: Aug 13, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Serum amyloid A IVD, kit, nephelometry/turbidimetry
Type: IVD General

Manufacturer

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

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About this record

Serum amyloid A IVD, kit, nephelometry/turbidimetry is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 175369. 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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