Assisted reproduction embryo-assessment software - UK MHRA Medical Device Registration

Assisted reproduction embryo-assessment software is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 100812. The device is manufactured by Genea Biomedx Pty Ltd from Australia, classified as General Medical Device. The authorized representative in the UK is Donawa Lifescience 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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Assisted reproduction embryo-assessment software

MHRA Device ID: 100812•Ref: 100812

Device Type

General Medical Device

Devices

Assisted reproduction embryo-assessment software

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Feb 6, 2024

Manufacturer Information

Name

Genea Biomedx Pty Ltd

Address

Level 2 321 Kent Street

Sydney, Australia

Created Date

May 4, 2021

Authorized Representative

Name

Donawa Lifescience Ltd

Relationship Type

UK Responsible Person

Address

Aviation Business Park Enterprise Close

Christchurch, England, United Kingdom

Postcode: BH23 6NX

DJ Fang

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Assisted reproduction embryo-assessment software - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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