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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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VISIOLITE MASTER GT — 2 UDI-DI variants, MDR (FIM Médical)

MD Atlas
FIM Médical

Data from EUDAMED, last updated May 19, 2026

VISIOLITE MASTER GT

376025345FF1017TE

2 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: FIM Médical

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 376025345FF1017TE
Device name: VISIOLITE MASTER GT
Device model: VISIOLITE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 2, 2022

Manufacturer & authorised representative

Manufacturer

Name: FIM Médical
SRN: FR-MF-000017090
Country: France
Email: contact@fim-medical.com
Phone: +33472348989

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G9EPF44T50Z5PX3SHDHC67C9

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

FF105503760253450089
VISIOLITE MASTER Edition Computerized03760253450119