United Kingdom MHRA device registration 203832

Zika virus immunoglobulin M (IgM) antibody IVD, kit, chemiluminescent immunoassay

United Kingdom·In Vitro Diagnostic Device·DIA.PRO Diagnostic Bioprobes S.r.l.·Registered Nov 26, 2024

Registration details

Device ID: 203832
MHRA Reference Number: 203832
Date Registered: Nov 26, 2024
Last Updated: Oct 26, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Zika virus immunoglobulin M (IgM) antibody IVD, kit, chemiluminescent immunoassay
Type: IVD General

Manufacturer

Name: DIA.PRO Diagnostic Bioprobes S.r.l.
Address: Via Giosuè Carducci, 27 20099 Sesto San Giovanni
Milan, Italy
Created Date: Oct 24, 2024

Authorized Representative

Name: A. Menarini Diagnostics Ltd.
Relationship Type: UK Responsible Person
Address: 405 Wharfedale Road
Wokingham, Berkshire, England, United Kingdom
Postcode: RG41 5RA

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About this record

Zika virus immunoglobulin M (IgM) antibody IVD, kit, chemiluminescent immunoassay is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 203832. The device is manufactured by DIA.PRO Diagnostic Bioprobes S.r.l. from Italy, classified as In Vitro Diagnostic Device. The authorized representative in the UK is A. Menarini Diagnostics Ltd..

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