United Kingdom MHRA device registration 42546

Echovirus antigen (serotypes EV1-EV33) IVD, kit, enzyme immunoassay (EIA)

United Kingdom·In Vitro Diagnostic Device·EMD Millipore Corporation·Registered Jul 17, 2018

Registration details

Device ID: 42546
MHRA Reference Number: 42546
Date Registered: Jul 17, 2018
Last Updated: Aug 5, 2023

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Echovirus antigen (serotypes EV1-EV33) IVD, kit, enzyme immunoassay (EIA)
Type: IVD General

Manufacturer

Name: EMD Millipore Corporation
Address: 28820 Single Oak Drive Temecula
Temecula, California, United States
Created Date: Jul 17, 2018

Authorized Representative

Name: Millipore (UK) Ltd
Relationship Type: UK Responsible Person
Address: 2 Fleming Road Kirkton Campus
Livingston, West Lothian, Scotland, United Kingdom
Postcode: EH54 7BN

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About this record

Echovirus antigen (serotypes EV1-EV33) IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 42546. The device is manufactured by EMD Millipore Corporation from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Millipore (UK) Ltd.

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