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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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Pas brzuszny pooperacyjny (z 3… — 7 UDI-DI variants, MDR

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

Data from EUDAMED, last updated May 31, 2026

Pas brzuszny pooperacyjny (z 3 niezależnymi rzepami)

590464771301567

7 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: 590464771301567
Device name: Pas brzuszny pooperacyjny (z 3 niezależnymi rzepami)
Device model: MEK 3015
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 8, 2025

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

7 UDI-DI variants

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Applied filters

basicUdiUlid01K24ZT1K9F6A8FAZZ4ZPB4QCG

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

Postoperative abdominal belt05904647710986
Postoperative abdominal belt05904647710856
Postoperative abdominal belt05904647710993
Postoperative abdominal belt05904647710849
Postoperative abdominal belt05904647710870
Postoperative abdominal belt05904647710221
Postoperative abdominal belt05904647710863