Legionella pneumophila immunoglobulin A (IgA)/IgG/IgM antibody IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

Legionella pneumophila immunoglobulin A (IgA)/IgG/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 97546. The device is manufactured by Vircell, S.L. from Spain, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Launch Diagnostics Limited.

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Legionella pneumophila immunoglobulin A (IgA)/IgG/IgM antibody IVD, kit, enzyme immunoassay (EIA)

MHRA Device ID: 97546•Ref: 97546

Device Type

In Vitro Diagnostic Device

Devices

Legionella pneumophila immunoglobulin A (IgA)/IgG/IgM antibody IVD, kit, enzyme immunoassay (EIA)

Type

IVD General

Date Registered

Aug 23, 2024

Last Updated

Apr 5, 2024

Manufacturer Information

Name

Vircell, S.L.

Address

Parque Tecnológico de la Salud Avicena 8

Granada, Spain

Created Date

Jul 9, 2021

Authorized Representative

Name

Launch Diagnostics Limited

Relationship Type

UK Responsible Person

Address

Unit 20 Ash Way Thorp Arch Estate

Wetherby, England, United Kingdom

Postcode: LS23 7FA

DJ Fang

MedTech Regulatory Expert

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Legionella pneumophila immunoglobulin A (IgA)/IgG/IgM antibody IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

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