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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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VWR Nitrile extra light gloves — 5 UDI-DI variants, MDR

MD Atlas
VWR International bv

Data from EUDAMED, last updated May 23, 2026

VWR Nitrile extra light gloves

731205T005AG

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: VWR International bv

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 731205T005AG
Device name: VWR Nitrile extra light gloves
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 29, 2025

Manufacturer & authorised representative

Manufacturer

Name: VWR International bv
SRN: BE-MF-000016952
Country: Belgium
Email: belgium_regulatory_affairs@vwr.com
Phone: +32 16 385 011

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01K6AM6ZDSY8ZYJXXSVA0BJAR3

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

GLOVE NITRILE PF EXTRA LIGHT L(8-9)07312056676881
GLOVE NITRILE PF EXTRA LIGHT M(7-8)07312056676874
GLOVE NITRILE PF EXTRA LIGHT S(6-7)07312056676867
GLOVE NITRILE PF EXTRA LIGHT XL(9-10)07312056676898
GLOVE NITRILE PF EXTRA LIGHT XS(5-6)07312056676850