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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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EYEXPLOR FRAMIRAL — 3 UDI-DI variants, MDR (FRAMIRAL)

MD Atlas
FRAMIRAL

Data from EUDAMED, last updated May 19, 2026

EYEXPLOR FRAMIRAL

376036468FRAMI-EYEX3N

3 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: FRAMIRAL

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 376036468FRAMI-EYEX3N
Device name: EYEXPLOR FRAMIRAL
Device model: EYEXPLOR
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 18, 2025

Manufacturer & authorised representative

Manufacturer

Name: FRAMIRAL
SRN: FR-MF-000011744
Country: France
Email: contact@framiral.fr

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K5ED4SN76CZVVVPQGSSMEAXY

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

FRAMI-EYEXPLOR03760364680276
Frami-EyeXplor Module Sinusoïdal03760364680214
Frami-EyeXplor module vAGST03760364680221