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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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Temblak do podnoszenia ramienia — 4 UDI-DI variants, MDR

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

Data from EUDAMED, last updated May 30, 2026

Temblak do podnoszenia ramienia

590464771400163

4 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: 590464771400163
Device name: Temblak do podnoszenia ramienia
Device model: MEK 4001
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 23, 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

4 UDI-DI variants

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Applied filters

basicUdiUlid01KMBXP82N878PWVFNDH94F3WK

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

4001-xsm-cz05904647710504
4001-lxxl-cz05904647710825
4001-xsm-sz05904647710115
4001-lxxl-sz05904647710832