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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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Comcord / Włókno kompozytowe — 6 UDI-DI variants, MDR

MD Atlas
ARKONA Laboratorium Farmakologii Stomatologicznej Grzegorz Kalbarczyk

Data from EUDAMED, last updated May 30, 2026

Comcord / Włókno kompozytowe

590443371TF0227E

6 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: ARKONA Laboratorium Farmakologii Stomatologicznej Grzegorz Kalbarczyk

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Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 590443371TF0227E
Device name: Comcord / Włókno kompozytowe
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 11, 2026

Manufacturer & authorised representative

Manufacturer

Name: ARKONA Laboratorium Farmakologii Stomatologicznej Grzegorz Kalbarczyk
SRN: PL-MF-000029550
Country: Poland
Email: biuro@arkonadent.com
Phone: +48 887 883 001

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KH5RAJ4FXMGSW7K9AE6EM98X

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

Comcord05904433718288
Comcord A305904433718363
Comcord A3.505904433718851
-05904433711876
-05904433718356
-05904433718844