Posterior eye segment analyser software - UK MHRA Medical Device Registration

Posterior eye segment analyser software is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 95178. 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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Posterior eye segment analyser software

MHRA Device ID: 95178•Ref: 95178

Device Type

General Medical Device

Devices

Posterior eye segment analyser 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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Posterior eye segment analyser software - UK MHRA Medical Device Registration

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Date Registered

Last Updated

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Address

Created Date

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DJ Fang

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