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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 — 10 UDI-DI variants, MDR

MD Atlas
Ansell Healthcare Europe NV

Data from EUDAMED, last updated May 23, 2026

Nitrile Examination/Treatment Glove

5414566MTNITT700S3

10 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: 5414566MTNITT700S3
Device name: Nitrile Examination/Treatment Glove
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 29, 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

10 UDI-DI variants

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Applied filters

basicUdiUlid01HGDNANYN473EVMT0PCSBHJMC

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

700114 Size L25414566720538
700112 Size S25414566720514
700111 Size XS25414566720507
700113 Size M25414566720521
700115 Size XL25414566720545
700121 Size XS25414566720606
700123 Size M25414566720620
700124 Size L25414566720637
700125 Size XL25414566720644
700122 Size S25414566720613