United Kingdom MHRA device registration 160204

Neutrophil gelatinase-associated lipocalin (NGAL) IVD, kit, fluorescent immunoassay

United Kingdom·In Vitro Diagnostic Device·CITEST DIAGNOSTICS INC·Registered Nov 26, 2024

Registration details

Device ID: 160204
MHRA Reference Number: 160204
Date Registered: Nov 26, 2024
Last Updated: May 14, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Neutrophil gelatinase-associated lipocalin (NGAL) IVD, kit, fluorescent immunoassay
Type: IVD General

Manufacturer

Name: CITEST DIAGNOSTICS INC
Address: 170-422 Richards Street Vancouver BC V6B 2Z4 Canada
Vancouver, Canada
Created Date: Aug 3, 2021

Authorized Representative

Name: UK RepMed Ltd.
Relationship Type: UK Responsible Person
Address: Unit D, Crondall Place Coxbridge Business Park Alton Road Farnham, Surrey,
Farnham, England, United Kingdom
Postcode: GU10 5EH

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About this record

Neutrophil gelatinase-associated lipocalin (NGAL) IVD, kit, fluorescent immunoassay is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 160204. The device is manufactured by CITEST DIAGNOSTICS INC from Canada, classified as In Vitro Diagnostic Device. The authorized representative in the UK is UK RepMed Ltd..

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