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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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Huśtawka terapeutyczna typu… — 10 UDI-DI variants, MDR

MD Atlas
Artur Tywonek Praksja Dystrybucja

Data from EUDAMED, last updated Jun 2, 2026

Huśtawka terapeutyczna typu „Platforma” 140x50 cm

590799044platforma140NV

10 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: Artur Tywonek Praksja Dystrybucja

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 590799044platforma140NV
Device name: Huśtawka terapeutyczna typu „Platforma” 140x50 cm
Device model: Platforma 140x50
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 30, 2026

Manufacturer & authorised representative

Manufacturer

Name: Artur Tywonek Praksja Dystrybucja
SRN: PL-MF-000053577
Country: Poland
Email: dystrybucja@praksja.pl
Phone: +48 601205537

Variants by status

UDI-DI variants

10 UDI-DI variants

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Applied filters

basicUdiUlid01KSWQEQYDE48CJDSZ5R6HSXPT

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

PR-153259079904408218
PR-102359079904408072
PR-075259079904407464
PR-102259079904407532
PR-102159079904407600
PR-102059079904407396
PR-153159079904408140
PR-102659079904407846
PR-102559079904407778
PR-102459079904407914