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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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Test tube — 2 UDI-DI variants, IVDR (Golias d.o.o.)

MD Atlas
Golias d.o.o.

Data from EUDAMED, last updated May 31, 2026

Test tube

383003667TUBETEST6E

2 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: Golias d.o.o.

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 383003667TUBETEST6E
Device name: —
Device model: Test tube
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: Golias d.o.o.
SRN: SI-MF-000006917
Country: Slovenia
Email: info@golias.si
Phone: +386 (0)1 429 70 10

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS50APQQFCXH39YRV0BGPRRH

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

Test tube 12 x 75mm03830036677115
Test tube 16 x 100mm03830036677535