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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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Aparat odwodzący kończynę górną z klinem — 3 UDI-DI variants, MDR

MD Atlas
MEK-ORTO Sp. z o.o.

Data from EUDAMED, last updated May 31, 2026

Aparat odwodzący kończynę górną z klinem

590464771400265

3 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: MEK-ORTO Sp. z o.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 590464771400265
Device name: Aparat odwodzący kończynę górną z klinem
Device model: MEK 4002
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 30, 2026

Manufacturer & authorised representative

Manufacturer

Name: MEK-ORTO Sp. z o.o.
SRN: PL-MF-000019251
Country: Poland
Email: sklep@mekorto.pl
Phone: +48 502 246 353

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KQEAA8XFESKGBS4XSYVEXCVE

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

4002-cz-l05904647710023
4002-cz-sm05904647711020
4002-cz-xl05904647711013