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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 Glove XS — 5 UDI-DI variants, MDR

MD Atlas
Wellgio Medical Oy Ltd

Data from EUDAMED, last updated May 23, 2026

Nitrile Examination Glove XS

643007964WG-11013G

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: Wellgio Medical Oy Ltd

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 643007964WG-11013G
Device name: Nitrile Examination Glove XS
Device model: WG-1101
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 17, 2023

Manufacturer & authorised representative

Manufacturer

Name: Wellgio Medical Oy Ltd
SRN: FI-MF-000033705
Country: Finland
Email: info@wellgio.com
Phone: +358405405363

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01GT7BQDXXXD5MQZCC05E9ADQB

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

Wellgio Nitrile Examination Glove L06430079640045
Wellgio Nitrile Examination Glove M06430079640038
Wellgio Nitrile Examination Glove S06430079640021
Wellgio Nitrile Examination Glove XL06430079640052
Wellgio Nitrile Examination Glove XS06430079640014