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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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Antykoagulanty do pobierania krwi — 9 UDI-DI variants, IVDR

MD Atlas
KOLASA SPÓŁKA JAWNA

Data from EUDAMED, last updated May 30, 2026

Antykoagulanty do pobierania krwi

590649294ADPKJN

9 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: KOLASA SPÓŁKA JAWNA

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 590649294ADPKJN
Device name: Antykoagulanty do pobierania krwi
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Mar 17, 2025

Manufacturer & authorised representative

Manufacturer

Name: KOLASA SPÓŁKA JAWNA
SRN: PL-MF-000044993
Country: Poland
Email: m.brandebura@aqu-med.pl

Variants by status

UDI-DI variants

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JP2D3PK3WH4MYZKRG3KAVDTW

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

2001.505906492941041
2001.205906492941065
2001.305906492941058
2005.505906492941096
2005.205906492941072
2005.305906492941089
2002.505906492941102
2002.205906492941126
2002.305906492941119