United Kingdom MHRA device registration 181497

Multiple drugs of abuse IVD, kit, rapid ICT, clinical

United Kingdom·In Vitro Diagnostic Device·LumiQuick Diagnostics Inc.·Registered Nov 26, 2024

Registration details

Device ID: 181497
MHRA Reference Number: 181497
Date Registered: Nov 26, 2024
Last Updated: Aug 13, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Multiple drugs of abuse IVD, kit, rapid ICT, clinical
Type: IVD General

Manufacturer

Name: LumiQuick Diagnostics Inc.
Address: 2946 Scott Blvd
Santa Clara, California, United States
Created Date: Nov 9, 2023

Authorized Representative

Name: Qarad UK Ltd.
Relationship Type: UK Responsible Person
Address: 8 Northumberland Ave
Westminster, London , England, United Kingdom
Postcode: WC2N 5BY

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About this record

Multiple drugs of abuse IVD, kit, rapid ICT, clinical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 181497. The device is manufactured by LumiQuick Diagnostics Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qarad UK Ltd..

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