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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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Non-Powdered Latex Surgical Gloves — 8 UDI-DI variants, MDR

MD Atlas
Ansell Healthcare Europe NV

Data from EUDAMED, last updated May 23, 2026

Non-Powdered Latex Surgical Gloves

5414566GLGIG330083NZ

8 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Ansell Healthcare Europe NV

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5414566GLGIG330083NZ
Device name: Non-Powdered Latex Surgical Gloves
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 4, 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

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GTPNMTKVAC477BECT1WBV636

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

330083090 915414566832906
330083060 615414566832609
330083075 7.515414566832753
330083055 5.515414566832555
330083080 815414566832807
330083065 6.515414566832654
330083070 715414566832708
330083085 8.515414566832852