United Kingdom MHRA device registration 130318

Urea IVD, kit, enzyme spectrophotometry

United Kingdom·In Vitro Diagnostic Device·HORIBA ABX SAS·Registered Nov 26, 2024

Registration details

Device ID: 130318
MHRA Reference Number: 130318
Date Registered: Nov 26, 2024
Last Updated: Oct 10, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Urea IVD, kit, enzyme spectrophotometry
Type: IVD General

Manufacturer

Name: HORIBA ABX SAS
Address: Parc Euromédecine - Rue du Caducée BP 7290
34184 Montpellier, France
Created Date: Nov 24, 2021

Authorized Representative

Name: HORIBA UK Limited
Relationship Type: UK Responsible Person
Address: KYOTO CLOSE MOULTON PARK
NORTHAMPTON, Northants, United Kingdom
Postcode: NN3 6FL

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About this record

Urea IVD, kit, enzyme spectrophotometry is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 130318. The device is manufactured by HORIBA ABX SAS from France, classified as In Vitro Diagnostic Device. The authorized representative in the UK is HORIBA UK Limited.

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