Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

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

MD Atlas
Artur Tywonek Praksja Dystrybucja

Data from EUDAMED, last updated May 31, 2026

Huśtawka terapeutyczna typu „Platforma” 100x50 cm

590799044platforma100NH

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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 590799044platforma100NH
Device name: Huśtawka terapeutyczna typu „Platforma” 100x50 cm
Device model: Platforma 100x50
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 29, 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

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KSST580022QMAX3CB4NTS0G9

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-001459079904408386
PR-103159079904406238
PR-103259079904406092
PR-103359079904405934
PR-102959079904408454
PR-153059079904406610
PR-103059079904406160
PR-102859079904406306
PR-102759079904406474
PR-152959079904406542