United Kingdom MHRA device registration 161273

Assisted reproduction embryo-assessment software

United Kingdom flagUnited Kingdom·General Medical Device·Fairtility Ltd·Registered Nov 26, 2024
Registration details
Device ID
161273
MHRA Reference Number
161273
Date Registered
Nov 26, 2024
Last Updated
Mar 23, 2024
Device classification
Device Type
General Medical Device
Devices
Assisted reproduction embryo-assessment software
Type
Class I
Manufacturer
Address
8 Ha'Melacha St
-, Tel-Aviv, Israel
Created Date
Nov 21, 2022
Authorized Representative
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 161273. The device is manufactured by Fairtility 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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