United Kingdom MHRA device registration 125882

Cancer risk assessment interpretive software IVD

United Kingdom·In Vitro Diagnostic Device·Genomic Health, Inc.·Registered Dec 22, 2021

Registration details

Device ID: 125882
MHRA Reference Number: 125882
Date Registered: Dec 22, 2021
Last Updated: Oct 12, 2023

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Cancer risk assessment interpretive software IVD
Type: IVD General

Manufacturer

Name: Genomic Health, Inc.
Address: 301 Penobscot Drive
Redwood City, California, United States
Created Date: Dec 22, 2021

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

Cancer risk assessment interpretive software IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 125882. The device is manufactured by Genomic Health, Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qarad UK Ltd..

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