United Kingdom MHRA device registration 137295

Mycoplasma pneumoniae immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)

United Kingdom·In Vitro Diagnostic Device·NeoMedica doo·Registered Apr 11, 2024

Registration details

Device ID: 137295
MHRA Reference Number: 137295
Date Registered: Apr 11, 2024
Last Updated: Oct 17, 2023

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Mycoplasma pneumoniae immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)
Type: IVD General

Manufacturer

Name: NeoMedica doo
Address: Bulevar Svetog Cara Konstantina 82-86,
Nis, Serbia
Created Date: Nov 26, 2020

Authorized Representative

Name: Wellkang Ltd
Relationship Type: Authorised Representative (Northern Ireland)
Address: Enterprise Hub, NW Business Complex 1 Beraghmore Road
Derry, Northern Ireland, Northern Ireland, United Kingdom
Postcode: BT48 8SE

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About this record

Mycoplasma pneumoniae immunoglobulin M (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 137295. The device is manufactured by NeoMedica doo from Serbia, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Wellkang Ltd.

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