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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 Lite Latex Free - URGO KTwo… — 12 UDI-DI variants, MDR

MD Atlas
LABORATOIRES URGO

Data from EUDAMED, last updated May 19, 2026

URGO K2 Lite Latex Free - URGO KTwo Reduced Latex Free

354689UM00785M

12 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: 354689UM00785M
Device name: URGO K2 Lite Latex Free - URGO KTwo Reduced Latex Free
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 23, 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

12 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G68M4MDGDQ0AE5038Y0W0EA2

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

60588203546890051069
60596803546890051298
60525203546890050130
60596903546890051304
60525403546890050147
60588303546890051076
55291203546890029532
55293603546890029372
55291103546890029549
55293703546890029365
URGO KTwo Reduced Latex Free03546890029631
URGO KTwo Reduced Latex Free03546890029624