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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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Stabilizator stawu skokowego — 12 UDI-DI variants, MDR

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

Data from EUDAMED, last updated May 30, 2026

Stabilizator stawu skokowego

590464771900176

12 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: 590464771900176
Device name: Stabilizator stawu skokowego
Device model: MEK 9001
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

12 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KQEWYXDSTF5PBFA0V960P52X

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

9001-bz-l05904647710955
9001-bz-m05904647710948
9001-bz-s05904647710931
9001-bz-xl05904647710962
9001-bz-xs05904647710436
9001-bz-2xl05904647710979
9001-cz-l05904647711044
9001-cz-m05904647711051
9001-cz-s05904647711068
9001-cz-xl05904647711075
9001-cz-xs05904647711099
9001-cz-xxl05904647711082