United Kingdom MHRA device registration 102676

Human genomic analysis interpretive software

United Kingdom·In Vitro Diagnostic Device·Omixon Biocomputing Ltd.·Registered Nov 26, 2024

Registration details

Device ID: 102676
MHRA Reference Number: 102676
Date Registered: Nov 26, 2024
Last Updated: Oct 1, 2024

Device classification

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

Manufacturer

Name: Omixon Biocomputing Ltd.
Address: Kaposvar u.14-18,
Budapest, Hungary
Created Date: Sep 3, 2021

Authorized Representative

Name: Emergo Consulting (UK) Limited
Relationship Type: UK Responsible Person
Address: Compass House, Vision Park Histon c/o Cr360 – UL International
Cambridge, England, United Kingdom
Postcode: CB24 9BZ

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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 102676. The device is manufactured by Omixon Biocomputing Ltd. from Hungary, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Emergo Consulting (UK) Limited .

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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