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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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Laska inwalidzka — 4 UDI-DI variants, MDR (ACTION SPÓŁKA AKCYJNA)

MD Atlas
ACTION SPÓŁKA AKCYJNA

Data from EUDAMED, last updated May 31, 2026

Laska inwalidzka

5901443LISU

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: ACTION SPÓŁKA AKCYJNA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5901443LISU
Device name: Laska inwalidzka
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 21, 2025

Manufacturer & authorised representative

Manufacturer

Name: ACTION SPÓŁKA AKCYJNA
SRN: PL-MF-000046182
Country: Poland
Email: action@action.pl
Phone: +48 22 332 16 00

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01K0P5257ABR0JK9MN4JT0H9ZA

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

LI200AM05901443001645
LI201AM05901443002185
LI100AM05901443000969
LI101AM05901443001164