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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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URGOSTART Plus Absorb - URGOSTART Plus… — 16 UDI-DI variants, MDR

MD Atlas
LABORATOIRES URGO

Data from EUDAMED, last updated May 19, 2026

URGOSTART Plus Absorb - URGOSTART Plus Non Border

354689UM014357

16 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

Animal tissues / cells

Identity & classification

Basic UDI-DI: 354689UM014357
Device name: URGOSTART Plus Absorb - URGOSTART Plus Non Border
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Sep 14, 2023

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

16 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HA9K8AAKTGY2YQEYNCJHQWTP

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

75423103546890030767
60420103546890047253
URGOSTART Plus Absorb03546890041343
60419003546890047215
60420303546890047277
60298203546890042326
URGOSTART Plus Absorb03546890042364
60420203546890047260
60418503546890047208
60419303546890047222
75423203546890030460
60298003546890042296
60298403546890042340
75420103546890030958
75419603546890040278
60298303546890042333