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

Mumps virus immunoglobulin A (IgA)/IgG/IgM antibody IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 195655. The device is manufactured by TestLine Clinical Diagnostics s.r.o from Czechia, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Oxford Biosystems 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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Mumps virus immunoglobulin A (IgA)/IgG/IgM antibody IVD, kit, enzyme immunoassay (EIA)

MHRA Device ID: 195655•Ref: 195655

Device Type

In Vitro Diagnostic Device

Devices

Mumps virus immunoglobulin A (IgA)/IgG/IgM antibody IVD, kit, enzyme immunoassay (EIA)

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Nov 12, 2024

Manufacturer Information

Name

TestLine Clinical Diagnostics s.r.o

Address

Křižíkova 188/68

Brno, Czechia

Created Date

Nov 24, 2022

Authorized Representative

Name

Oxford Biosystems Ltd

Relationship Type

UK Responsible Person

Address

184B Park Drive Milton Park Abingdon

Abingdon, Oxfordshire, United Kingdom

Postcode: OX14 4SE

DJ Fang

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

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