United Kingdom MHRA device registration 144619

Human genomic analysis interpretive software IVD

United Kingdom·In Vitro Diagnostic Device·23andMe, Inc.·Registered Nov 26, 2024

Registration details

Device ID: 144619
MHRA Reference Number: 144619
Date Registered: Nov 26, 2024
Last Updated: May 9, 2024

Device classification

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

Manufacturer

Name: 23andMe, Inc.
Address: 349 Oyster Point Blvd
South San Francisco, California, United States
Created Date: Apr 13, 2022

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

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 144619. The device is manufactured by 23andMe, Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qarad UK Ltd..

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