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 203201. The device is manufactured by Kai Health, Inc from South Korea, classified as General Medical Device. The authorized representative in the UK is CMC Medical Devices 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.
Device Type
General Medical Device
Devices
Assisted reproduction embryo-assessment software
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Oct 17, 2024
Name
Kai Health, IncAddress
B2-Google Startups Campus, 417, Yeongdong- daero, Gangnam-gu,
Seoul,, South Korea
Created Date
Oct 16, 2024
Relationship Type
Address
Office 32 19-21 Crawford Street
London, United Kingdom
Postcode: W1H 1PJ
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