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 103912. The device is manufactured by One Lambda, Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qarad UK Ltd..

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Human genomic analysis interpretive software

MHRA Device ID: 103912•Ref: 103912

Device Type

In Vitro Diagnostic Device

Devices

Human genomic analysis interpretive software

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Aug 6, 2024

Manufacturer Information

Name

One Lambda, Inc.

Address

22801 Roscoe Blvd.

West Hills, California, United States

Created Date

Sep 14, 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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DJ Fang

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