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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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URGOTUL — 43 UDI-DI variants, MDR (LABORATOIRES URGO)

MD Atlas
LABORATOIRES URGO

Data from EUDAMED, last updated May 19, 2026

URGOTUL

354689UM00234U

43 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

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 354689UM00234U
Device name: URGOTUL
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jan 7, 2026

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

43 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KEBTHV62ZWTFD8495P17MQTZ

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

60291203546890042104
60333203546890043408
60330303546890043279
60433603546890048113
60436703546890048359
60290903546890042074
60429603546890047956
60435203546890048243
60436403546890048328
60439203546890048434
60437003546890048373
60436903546890048366
60429403546890047949
60290503546890042043
60435403546890048267
60427203546890047772
60423103546890047598
60427703546890047857

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