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 95179. The device is manufactured by NIDEK CO., LTD. from Japan, classified as General Medical Device. The authorized representative in the UK is Advena 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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Retinal image analysis software

MHRA Device ID: 95179•Ref: 95179

Device Type

General Medical Device

Devices

Retinal image analysis software

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Apr 13, 2024

Manufacturer Information

Name

NIDEK CO., LTD.

Address

34-14 Maehama Hiroishi-cho Gamagori

Aichi , Japan

Created Date

Apr 22, 2021

Authorized Representative

Name

Advena Ltd

Relationship Type

UK Responsible Person

Address

Pure Offices Plato Close

Warwick, England, United Kingdom

Postcode: CV34 6WE

DJ Fang

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Other Products from NIDEK CO., LTD. (10)

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Retinal image analysis software - UK MHRA Medical Device Registration

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Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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