United Kingdom MHRA device registration 100008

Human genomic analysis interpretive software

United Kingdom·In Vitro Diagnostic Device·Natera, Inc·Registered Nov 26, 2024

Registration details

Device ID: 100008
MHRA Reference Number: 100008
Date Registered: Nov 26, 2024
Last Updated: Jul 2, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Human genomic analysis interpretive software
Type: IVD Annex II List B

Manufacturer

Name: Natera, Inc
Address: 201 Industrial Road, Suite 410
San Carlos, California, United States
Created Date: Aug 27, 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

Human genomic analysis interpretive software is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 100008. The device is manufactured by Natera, Inc from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qarad UK Ltd..

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