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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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URGOCLEAN Pad - URGOCLEAN Compresse -… — 12 UDI-DI variants, MDR

MD Atlas
LABORATOIRES URGO

Data from EUDAMED, last updated May 19, 2026

URGOCLEAN Pad - URGOCLEAN Compresse - URGOCLEAN Kompresse - URGOCLEAN Compresa

354689UM00695L

12 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: 354689UM00695L
Device name: URGOCLEAN Pad - URGOCLEAN Compresse - URGOCLEAN Kompresse - URGOCLEAN Compresa
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Aug 25, 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

12 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K3GNX292S4P2AVSZHMKQGAY0

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

60326403546890043040
60327003546890043088
60336503546890043545
60326303546890043026
60340503546890043590
60340603546890043606
60335703546890043477
60341103546890043613
60334503546890043439
60343303546890043668
60335503546890043460
60326703546890043057