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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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URGO K1 - URGO KOne — 18 UDI-DI variants, MDR (LABORATOIRES URGO)

MD Atlas
LABORATOIRES URGO

Data from EUDAMED, last updated May 19, 2026

URGO K1 - URGO KOne

354689UM01535A

18 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: LABORATOIRES URGO

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 354689UM01535A
Device name: URGO K1 - URGO KOne
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 23, 2024

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

18 UDI-DI variants

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Applied filters

basicUdiUlid01G6A73YD2NPWGKYRQH0N6P04Q

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

60254103546890031436
60192003546890039906
60412303546890046768
19314203546890039296
60113103546890038886
60412103546890046744
60113003546890038893
60113303546890038862
60192103546890037742
19315003546890039289
60254303546890033010
60311103546890042807
60113203546890038879
60412203546890046751
60412003546890046737
60311003546890042791
URGO KOne03546890044931
URGO KOne03546890044948