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 88782. The device is manufactured by AIVF Ltd from Israel, classified as General Medical Device. The authorized representative in the UK is Medimap 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: 88782•Ref: 88782

Device Type

General Medical Device

Devices

Assisted reproduction embryo-assessment software

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Jun 15, 2024

Manufacturer Information

Name

AIVF Ltd

Address

26 HaBarzel Street

Tel Aviv, Israel

Created Date

Jul 13, 2021

Authorized Representative

Name

Medimap Ltd

Relationship Type

UK Responsible Person

Address

2 The Drift

Thurston, Suffolk, United Kingdom

Postcode: IP31 3RT

DJ Fang

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

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