Retinal image analysis software - UK MHRA Medical Device Registration
Retinal image analysis software is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 122716. The device is manufactured by Verily Life Sciences LLC from United States, classified as General Medical Device. The authorized representative in the UK is Emergo Consulting (UK) Limited .
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
Retinal image analysis software
Type
Class IIa
Date Registered
Apr 11, 2024
Last Updated
Dec 9, 2022
Address
269 East Grand Avenue
South San Francisco, California, United States
Created Date
Dec 16, 2021
Relationship Type
Address
Compass House, Vision Park Histon c/o Cr360 โ UL International
Cambridge, England, United Kingdom
Postcode: CB24 9BZ
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