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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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Epruveta — 4 UDI-DI variants, IVDR (ŽIKPLAST Žitnik Anja s.p.)

MD Atlas
ŽIKPLAST Žitnik Anja s.p.

Data from EUDAMED, last updated May 31, 2026

Epruveta

383008604TESTTUBE85

4 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: ŽIKPLAST Žitnik Anja s.p.

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 383008604TESTTUBE85
Device name: Epruveta
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 23, 2026

Manufacturer & authorised representative

Manufacturer

Name: ŽIKPLAST Žitnik Anja s.p.
SRN: SI-MF-000054229
Country: Slovenia
Email: zikplast@siol.net

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRDQD91JQDRR7QBM6GB6PCW5

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

01198403830086040051
01198203830086040044
01200003830086040037
01197903830086040020