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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 light gloves — 5 UDI-DI variants, MDR

MD Atlas
VWR International bv

Data from EUDAMED, last updated May 23, 2026

VWR Nitrile light gloves

731205T004AE

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: 731205T004AE
Device name: VWR Nitrile 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

basicUdiUlid01K6AFBJBQCTPT3F3D7HX93B64

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 AMBI LIGHT POWDERFREE L07312056293538
GLOVE NITRILE AMBI LIGHT POWDERFREE M07312056293521
GLOVE NITRILE AMBI LIGHT POWDERFREE S07312056293514
GLOVE NITRILE AMBI LIGHT POWDERFREE XL07312056293545
GLOVE NITRILE AMBI LIGHT POWDERFREE XS07312056293590