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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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rtx1 adaptive optics retinal camera — 2 UDI-DI variants, MDR

MD Atlas
IMAGINE EYES

Data from EUDAMED, last updated May 19, 2026

rtx1 adaptive optics retinal camera

3770029591camera6J

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: IMAGINE EYES

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 3770029591camera6J
Device name: rtx1 adaptive optics retinal camera
Device model: rtx1 (MDR)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: IMAGINE EYES
SRN: FR-MF-000004148
Country: France
Email: qualite@imagine-eyes.com
Phone: +331 64 86 15 66

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KFDV53VJ6M13Q9F54FXK7NB4

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

RCTFI010037700295910384
RCSTD010037700295910216