United Kingdom MHRA device registration 153946

Cystic fibrosis IVD, kit, multiplex

United Kingdom·In Vitro Diagnostic Device·Luminex Corporation ·Registered Nov 26, 2024

Registration details

Device ID: 153946
MHRA Reference Number: 153946
Date Registered: Nov 26, 2024
Last Updated: Jul 6, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Cystic fibrosis IVD, kit, multiplex
Type: IVD General

Manufacturer

Name: Luminex Corporation
Address: 12212 Technology Blvd
Austin, Texas, United States
Created Date: Dec 23, 2021

Authorized Representative

Name: DiaSorin Italia S.p.A. UK Branch
Relationship Type: UK Responsible Person
Address: Central Road
Dartford, England, United Kingdom
Postcode: DA1 5LR

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About this record

Cystic fibrosis IVD, kit, multiplex is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 153946. The device is manufactured by Luminex Corporation from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is DiaSorin Italia S.p.A. UK Branch.

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