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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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Nitrile Examination Gloves,… — 5 UDI-DI variants, MDR (Prosenso ApS)

MD Atlas
Prosenso ApS

Data from EUDAMED, last updated May 31, 2026

Nitrile Examination Gloves, Accelerator-free, Biodegradable, Powder Free, Chlorinated, Non-Sterile

5745000094EB2011HR

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: Prosenso ApS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5745000094EB2011HR
Device name: Nitrile Examination Gloves, Accelerator-free, Biodegradable, Powder Free, Chlorinated, Non-Sterile
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 20, 2025

Manufacturer & authorised representative

Manufacturer

Name: Prosenso ApS
SRN: DK-MF-000043015
Country: Denmark
Email: info@prosenso.com
Phone: +45 7070 1711

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

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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

EWBIO35MTG2-S05745000094264
EWBIO35MTG2-XL05745000094271
EWBIO35MTG2-L05745000094240
EWBIO35MTG2-M05745000094257
EWBIO35MTG2-XS05745000094288