Toxoplasma gondii immunoglobulin G (IgG) antibody IVD, control - UK MHRA Medical Device Registration

Toxoplasma gondii immunoglobulin G (IgG) antibody IVD, control is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 88472. 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.

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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Toxoplasma gondii immunoglobulin G (IgG) antibody IVD, control

MHRA Device ID: 88472•Ref: 88472

Device Type

In Vitro Diagnostic Device

Devices

Toxoplasma gondii immunoglobulin G (IgG) antibody IVD, control

Type

IVD Annex II List B

Date Registered

Jul 12, 2021

Last Updated

Oct 13, 2022

Manufacturer Information

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

DJ Fang

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Other Products from Virion\Serion GmbH (10)

Other Products from Same Authorized Representative (10)

Toxoplasma gondii immunoglobulin G (IgG) antibody IVD, control - UK MHRA Medical Device Registration

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Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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