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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/treatment glove — 6 UDI-DI variants, MDR

MD Atlas
Ansell Healthcare Europe NV

Data from EUDAMED, last updated May 23, 2026

Nitrile examination/treatment glove

5414566MF93868FE

6 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: Ansell Healthcare Europe NV

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5414566MF93868FE
Device name: Nitrile examination/treatment glove
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 3, 2023

Manufacturer & authorised representative

Manufacturer

Name: Ansell Healthcare Europe NV
SRN: BE-MF-000000691
Country: Belgium
Email: samantha.marshall@ansell.com
Phone: +447919410683

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01GTHDVCB1RR5N8VQZE654DB30

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

93868120 XXXL10076490436411
93868080 M10076490436374
93868100 XL10076490436398
93868070 S10076490436367
93868090 L10076490436381
93868110 XXL10076490436404