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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 NITRILE GLOVES BLACK — 4 UDI-DI variants, MDR (Vik Dental d.o.o.)

MD Atlas
Vik Dental d.o.o.

Data from EUDAMED, last updated May 24, 2026

DORA NITRILE GLOVES BLACK

385989147510007Z9

4 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: 385989147510007Z9
Device name: DORA NITRILE GLOVES BLACK
Device model: 10007
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

4 UDI-DI variants

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Applied filters

basicUdiUlid01GWS6C0S3VB4A4H2Y08AV5JGN

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 NITRILE GLOVES BLACK L03859891475339
DORA NITRILE GLOVES BLACK M03859891475322
DORA NITRILE GLOVES BLACK S03859891475315
DORA NITRILE GLOVES BLACK XL03859891475346