United Kingdom MHRA device registration 95798

Cryptococcus neoformans antigen IVD, kit, rapid agglutination, clinical

United Kingdom·In Vitro Diagnostic Device·Meridian Bioscience Inc.·Registered Nov 26, 2024

Registration details

Device ID: 95798
MHRA Reference Number: 95798
Date Registered: Nov 26, 2024
Last Updated: Sep 10, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Cryptococcus neoformans antigen IVD, kit, rapid agglutination, clinical
Type: IVD General

Manufacturer

Name: Meridian Bioscience Inc.
Address: 3471 River Hills Drive
Cincinnati, OH, United States
Created Date: Aug 18, 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

Cryptococcus neoformans antigen IVD, kit, rapid agglutination, clinical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 95798. The device is manufactured by Meridian Bioscience Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Launch Diagnostics Limited.

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