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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 K2 - URGO KTwo — 40 UDI-DI variants, MDR (LABORATOIRES URGO)

MD Atlas
LABORATOIRES URGO

Data from EUDAMED, last updated May 19, 2026

URGO K2 - URGO KTwo

354689UM00314T

40 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: 354689UM00314T
Device name: URGO K2 - URGO KTwo
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 4, 2022

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

40 UDI-DI variants

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Applied filters

basicUdiUlid01G6MEXZWC603M8PXZCEND8RS9

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

No registered UDI-DI variants for this device family.