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Human genomic analysis interpretive software IVD - UK MHRA Medical Device Registration

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 165809. The device is manufactured by Ziwig from France, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Obelis 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.

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In Vitro Diagnostic Device
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Human genomic analysis interpretive software IVD
MHRA Device ID: 165809โ€ขRef: 165809

Device Type

In Vitro Diagnostic Device

Devices

Human genomic analysis interpretive software IVD

Type

IVD General

Date Registered

Oct 29, 2024

Last Updated

Jan 23, 2024

Manufacturer Information

Name

Ziwig

Address

19 rue Riboud

Lyon, France

Created Date

Feb 2, 2023

Authorized Representative

Relationship Type

UK Responsible Person

Address

Sandford Gate, East Point Business Park

Oxford , England, United Kingdom

Postcode: OX4 6LB

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