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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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Parawan medyczny — 6 UDI-DI variants, MDR (Tribo sp. z o.o.)

MD Atlas
Tribo sp. z o.o.

Data from EUDAMED, last updated May 31, 2026

Parawan medyczny

59051413467483QE

6 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: Tribo sp. z o.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 59051413467483QE
Device name: Parawan medyczny
Device model: 7483
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 22, 2025

Manufacturer & authorised representative

Manufacturer

Name: Tribo sp. z o.o.
SRN: PL-MF-000026942
Country: Poland
Email: tribo@tribo.com.pl

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JSEG0FJT6XEKNEPMB99KPHEX

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

Double medical screen05905141346442
Double medical screen05905141346459
Medical screen05905141346473
Medical screen05905141346466
Medical Screen05905141346480
748305905141346435