Cancer risk assessment interpretive software IVD - UK MHRA Medical Device Registration
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 185500. 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..
This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Device Type
In Vitro Diagnostic Device
Devices
Cancer risk assessment interpretive software IVD
Type
Class C
Date Registered
Nov 26, 2024
Last Updated
Oct 23, 2024
Address
301 Penobscot Drive
Redwood City, California, United States
Created Date
Dec 22, 2021
Name
Qarad UK Ltd.Relationship Type
Address
8 Northumberland Ave
Westminster, London , England, United Kingdom
Postcode: WC2N 5BY
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