United Kingdom MHRA device registration 121107

Human genomic analysis interpretive software IVD

United Kingdom·In Vitro Diagnostic Device·Agilent Technologies Belgium·Registered Nov 26, 2024

Registration details

Device ID: 121107
MHRA Reference Number: 121107
Date Registered: Nov 26, 2024
Last Updated: Nov 30, 2023

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Human genomic analysis interpretive software IVD
Type: IVD General

Manufacturer

Name: Agilent Technologies Belgium
Address: De Kleetlaan 5 bus 9
1831 Diegem, Belgium
Created Date: Dec 14, 2021

Authorized Representative

Name: Agilent Technologies LDA UK Limited
Relationship Type: UK Responsible Person
Address: 5500 Lakeside Cheadle Royal Business Park
Cheadle, Cheshire, England, United Kingdom
Postcode: SK8 3GR

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About this record

Human genomic analysis interpretive software IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 121107. The device is manufactured by Agilent Technologies Belgium from Belgium, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Agilent Technologies LDA UK Limited.

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