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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.

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Retinal image analysis software
MHRA Device ID: 122716โ€ขRef: 122716

Device Type

General Medical Device

Devices

Retinal image analysis software

Type

Class IIa

Date Registered

Apr 11, 2024

Last Updated

Dec 9, 2022

Manufacturer Information

Address

269 East Grand Avenue

South San Francisco, California, United States

Created Date

Dec 16, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

Compass House, Vision Park Histon c/o Cr360 โ€“ UL International

Cambridge, England, United Kingdom

Postcode: CB24 9BZ

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