Herpes simplex virus 1 & 2 (HSV1 & 2) immunoglobulin G (IgG)/IgM antibody IVD, reagent - UK MHRA Medical Device Registration

Herpes simplex virus 1 & 2 (HSV1 & 2) immunoglobulin G (IgG)/IgM antibody IVD, reagent is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 94113. 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.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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In Vitro Diagnostic Device

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Herpes simplex virus 1 & 2 (HSV1 & 2) immunoglobulin G (IgG)/IgM antibody IVD, reagent

MHRA Device ID: 94113•Ref: 94113

Device Type

In Vitro Diagnostic Device

Devices

Herpes simplex virus 1 & 2 (HSV1 & 2) immunoglobulin G (IgG)/IgM antibody IVD, reagent

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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Herpes simplex virus 1 & 2 (HSV1 & 2) immunoglobulin G (IgG)/IgM antibody IVD, reagent - UK MHRA Medical Device Registration

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DJ Fang

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