United Kingdom MHRA device registration 111996

Rubella virus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)

United Kingdom·In Vitro Diagnostic Device·ORGENTEC Diagnostika GmbH·Registered Aug 10, 2021

Registration details

Device ID: 111996
MHRA Reference Number: 111996
Date Registered: Aug 10, 2021
Last Updated: Oct 12, 2023

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Rubella virus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)
Type: IVD General

Manufacturer

Name: ORGENTEC Diagnostika GmbH
Address: Carl-Zeiss-Str. 49-51
Mainz, Rheinhessen-Pfalz, Germany
Created Date: Aug 10, 2021

Authorized Representative

Name: Qarad UK Ltd.
Relationship Type: UK Responsible Person
Address: 8 Northumberland Ave
Westminster, London , England, United Kingdom
Postcode: WC2N 5BY

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About this record

Rubella virus immunoglobulin G (IgG) 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 111996. The device is manufactured by ORGENTEC Diagnostika GmbH from Germany, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qarad UK Ltd..

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