Dengue virus immunoglobulin A (IgA)/IgG/IgM antibody IVD, kit, fluorescent immunoassay - UK MHRA Medical Device Registration

Dengue virus immunoglobulin A (IgA)/IgG/IgM antibody IVD, kit, fluorescent immunoassay is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 151830. The device is manufactured by Hangzhou Alltest Biotech Co Ltd from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Medimap Ltd.

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Dengue virus immunoglobulin A (IgA)/IgG/IgM antibody IVD, kit, fluorescent immunoassay

MHRA Device ID: 151830•Ref: 151830

Device Type

In Vitro Diagnostic Device

Devices

Dengue virus immunoglobulin A (IgA)/IgG/IgM antibody IVD, kit, fluorescent immunoassay

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Jun 15, 2024

Manufacturer Information

Name

Hangzhou Alltest Biotech Co Ltd

Address

#550 Yinhai Street Hangzhou Economic & Technological Development Area

Hangzhou, China

Created Date

Mar 9, 2021

Authorized Representative

Name

Medimap Ltd

Relationship Type

UK Responsible Person

Address

2 The Drift

Thurston, Suffolk, United Kingdom

Postcode: IP31 3RT

DJ Fang

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Dengue virus immunoglobulin A (IgA)/IgG/IgM antibody IVD, kit, fluorescent immunoassay - UK MHRA Medical Device Registration

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Address

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