Human genomic analysis interpretive software IVD - UK MHRA Medical Device Registration

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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Human genomic analysis interpretive software IVD

MHRA Device ID: 121107•Ref: 121107

Device Type

In Vitro Diagnostic Device

Devices

Human genomic analysis interpretive software IVD

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Nov 30, 2023

Manufacturer Information

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

DJ Fang

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Human genomic analysis interpretive software IVD - UK MHRA Medical Device Registration

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