Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

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

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Venoflex Incognito absolu — 295 UDI-DI variants, MDR (THUASNE)

MD Atlas
THUASNE

Data from EUDAMED, last updated May 19, 2026

Venoflex Incognito absolu

311179FR0001BE3

295 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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 311179FR0001BE3
Device name: Venoflex Incognito absolu
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

295 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01JXZWXWPT4AV4ZWWSYWF1KQC1

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

5023022030631303111790246510
5023022040151203111790246602
5020022040901303111790245735
5020022040152203111790245568
5020022020861203111790245186
5020022041061303111790097723
5020022040641203111790245681
5020022021062303111790097662
5025022030031203111790248040
5025022020031203111790247784
5023022020151203111790246329
5020022010901303111790244950
5025022020431303111790247876
5025022040861203111790248507
5020022010621203111790244844
5025022020432203111790247883
5025022010621203111790247647
5025022010631203111790247685
5025022030031303111790248057
5023022040431303111790246633
5020022020641303111790245179
5020022040631303111790245674
5020022020931203111790245223
5020022041062203111790097730
5020022010631203111790244882

1 2 3 4 5