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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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DORA POWDERED LATEX GLOVES — 5 UDI-DI variants, MDR

MD Atlas
Vik Dental d.o.o.

Data from EUDAMED, last updated May 24, 2026

DORA POWDERED LATEX GLOVES

385989147510002YX

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: Vik Dental d.o.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 385989147510002YX
Device name: DORA POWDERED LATEX GLOVES
Device model: 10002
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 30, 2023

Manufacturer & authorised representative

Manufacturer

Name: Vik Dental d.o.o.
SRN: HR-MF-000033824
Country: Croatia
Email: dijana@vik-dental.hr
Phone: +385 91 2334232

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01GWRWB2PEZT2TR26JRBSJZY24

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

DORA LATEX POWDERED GLOVES L03859891475872
DORA LATEX POWDERED GLOVES M03859891475865
DORA LATEX POWDERED GLOVES S03859891475841
DORA LATEX POWDERED GLOVES XL03859891475889
DORA LATEX POWDERED GLOVES xs03859891475858