United Kingdom MHRA device registration 88157

Chlamydia pneumoniae immunoglobulin M (IgM) antibody IVD, kit, chemiluminescent immunoassay

United Kingdom·In Vitro Diagnostic Device·Vircell, S.L.·Registered Aug 23, 2024

Registration details

Device ID: 88157
MHRA Reference Number: 88157
Date Registered: Aug 23, 2024
Last Updated: Apr 5, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Chlamydia pneumoniae immunoglobulin M (IgM) antibody IVD, kit, chemiluminescent immunoassay
Type: IVD Annex II List B

Manufacturer

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

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About this record

Chlamydia pneumoniae immunoglobulin M (IgM) antibody IVD, kit, chemiluminescent immunoassay is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 88157. 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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