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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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Gant d'examen Latex non poudré… — 5 UDI-DI variants, MDR

MD Atlas
LABORATOIRES EUROMEDIS

Data from EUDAMED, last updated May 19, 2026

Gant d'examen Latex non poudré EUROTEX® 240 MM

338936131RF

5 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 EUROMEDIS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 338936131RF
Device name: —
Device model: Gant d'examen Latex non poudré EUROTEX® 240 MM
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 24, 2026

Manufacturer & authorised representative

Manufacturer

Name: LABORATOIRES EUROMEDIS
SRN: FR-MF-000036597
Country: France
Email: service.qualite@euromedis.fr

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01HHPH71NRB7YRA79K6QFFCMBQ

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

Gant d'examen Latex non poudré EUROTEX® 240 MM Taille L03389360006042
Gant d'examen Latex non poudré EUROTEX® 240 MM Taille M03389360006059
Gant d'examen Latex non poudré EUROTEX® 240 MM Taille S03389360006066
Gant d'examen Latex non poudré EUROTEX® 240 MM Taille XL03389360006073
Gant d'examen Latex non poudré EUROTEX® 240 MM Taille XS03389360006080