Human genomic analysis interpretive software - UK MHRA Medical Device Registration

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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In Vitro Diagnostic Device

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Human genomic analysis interpretive software

MHRA Device ID: 100008•Ref: 100008

Device Type

In Vitro Diagnostic Device

Devices

Human genomic analysis interpretive software

Type

IVD Annex II List B

Date Registered

Nov 26, 2024

Last Updated

Jul 2, 2024

Manufacturer Information

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

DJ Fang

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Human genomic analysis interpretive software - UK MHRA Medical Device Registration

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Created Date

Name

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DJ Fang

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