United Kingdom MHRA device registration 88782

Assisted reproduction embryo-assessment software

United Kingdom·General Medical Device·AIVF Ltd·Registered Nov 26, 2024

Registration details

Device ID: 88782
MHRA Reference Number: 88782
Date Registered: Nov 26, 2024
Last Updated: Jun 15, 2024

Device classification

Device Type: General Medical Device
Devices: Assisted reproduction embryo-assessment software
Type: Class I

Manufacturer

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

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About this record

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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