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.

URGOFIT - URGOTÜL Flex — 13 UDI-DI variants, MDR (LABORATOIRES URGO)

MD Atlas
LABORATOIRES URGO

Data from EUDAMED, last updated May 19, 2026

URGOFIT - URGOTÜL Flex

354689UM01495K

13 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: LABORATOIRES URGO

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: 354689UM01495K
Device name: URGOFIT - URGOTÜL Flex
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Dec 2, 2025

Manufacturer & authorised representative

Manufacturer

Name: LABORATOIRES URGO
SRN: FR-MF-000002559
Country: France
Email: eudamed.lu@fr.urgo.com

Variants by status

UDI-DI variants

13 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

basicUdiUlid01KBFTE4HC61HF9GVYVVCR3AX6

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

60371203546890045662
60386203546890046188
60430803546890047994
60414103546890046911
60414303546890046935
60414403546890046942
60414203546890046928
60503103546890049820
60413703546890046904
60434903546890048229
60524003546890049981
60524703546890050079
60524203546890050017