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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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MATERAC — 5 UDI-DI variants, MDR ("LUBAWA" SPÓŁKA AKCYJNA)

MD Atlas
"LUBAWA" SPÓŁKA AKCYJNA

Data from EUDAMED, last updated May 31, 2026

MATERAC

59020968MATERACUD

5 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: "LUBAWA" SPÓŁKA AKCYJNA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 59020968MATERACUD
Device name: MATERAC
Device model: -MATERAC W POKROWCU NIEPRZEMAKALNYM, TRUDNOPALNYM, ANTYBAKTERYJNYM
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 19, 2025

Manufacturer & authorised representative

Manufacturer

Name: "LUBAWA" SPÓŁKA AKCYJNA
SRN: PL-MF-000046927
Country: Poland
Email: pwichrowska@lubawa.com.pl

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01K5GS8BFZYK5TZK8JB5KF1653

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

53011000059-075959020968030518
53011000060-075959020968030440
53011000064-075959020968031362
53011000051-075959020968030822
53011000053-075959020968030686