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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 nitrile OPTIFIRM vert taille S — 5 UDI-DI variants, MDR

MD Atlas
PAREDES DISTRIBUTION FRANCE

Data from EUDAMED, last updated May 19, 2026

Gant nitrile OPTIFIRM vert taille S

360690GTX0018ZP

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: PAREDES DISTRIBUTION FRANCE

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 360690GTX0018ZP
Device name: Gant nitrile OPTIFIRM vert taille S
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 22, 2025

Manufacturer & authorised representative

Manufacturer

Name: PAREDES DISTRIBUTION FRANCE
SRN: FR-MF-000047951
Country: France
Email: service.qualite@paredes.fr

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01K85EESXECE15ZEGQM85FWW80

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 Nitrile OPTIFIRM VERT taille L03606900021762
Gant Nitrile OPTIFIRM VERT taille M03606900021755
Gant Nitrile OPTIFIRM VERT taille S03606900021748
Gant Nitrile OPTIFIRM VERT taille XL03606900021779
Gant Nitrile OPTIFIRM VERT taille XXL03606900021786