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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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Venoflex Fantaisie — 12 UDI-DI variants, MDR (THUASNE)

MD Atlas
THUASNE

Data from EUDAMED, last updated May 19, 2026

Venoflex Fantaisie

311179FR0001KEM

12 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: THUASNE

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 311179FR0001KEM
Device name: Venoflex Fantaisie
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 17, 2025

Manufacturer & authorised representative

Manufacturer

Name: THUASNE
SRN: FR-MF-000001201
Country: France
Email: service.conseil@thuasne.fr
Phone: +33 4 77 81 40 40

Variants by status

UDI-DI variants

12 UDI-DI variants

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Applied filters

basicUdiUlid01JXZWZQ7H6778XXN17QN07XPQ

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

6323012011021303111790081593
6325012031021303111790076155
6325012031021203111790076148
6325012011021303111790076117
6323012021021303111790081616
6325012011021203111790076100
6323012031021203111790081623
6325012021021303111790076131
6325012021021203111790076124
6323012011021203111790081586
6323012031021303111790081630
6323012021021203111790081609