United Kingdom MHRA device registration 90248

Tick-borne encephalitis (TBE) virus immunoglobulin M (IgM) antibody IVD, control

United Kingdom·In Vitro Diagnostic Device·Virion\Serion GmbH·Registered Jul 12, 2021

Registration details

Device ID: 90248
MHRA Reference Number: 90248
Date Registered: Jul 12, 2021
Last Updated: Oct 13, 2022

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Tick-borne encephalitis (TBE) virus immunoglobulin M (IgM) antibody IVD, control
Type: IVD General

Manufacturer

Name: Virion\Serion GmbH
Address: Friedrich-Bergius-Ring 19
Wurzburg, Germany
Created Date: Jul 12, 2021

Authorized Representative

Name: Launch Diagnostics Limited
Relationship Type: UK Responsible Person
Address: Ash House Ash Road New Ash Green
Longfield, Kent, United Kingdom
Postcode: DA3 8JD

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About this record

Tick-borne encephalitis (TBE) virus immunoglobulin M (IgM) antibody IVD, control is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 90248. The device is manufactured by Virion\Serion GmbH from Germany, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Launch Diagnostics Limited.

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