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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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MEDORA — 7 UDI-DI variants, MDR (Reha-Bed Sp. z o.o.)

MD Atlas
Reha-Bed Sp. z o.o.

Data from EUDAMED, last updated May 31, 2026

MEDORA

59041832MEDORAKG

7 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: Reha-Bed Sp. z o.o.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 59041832MEDORAKG
Device name: MEDORA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 7, 2025

Manufacturer & authorised representative

Manufacturer

Name: Reha-Bed Sp. z o.o.
SRN: PL-MF-000040289
Country: Poland
Email: medical.devices@rehabed.com.pl
Phone: 32 346 00 33

Variants by status

UDI-DI variants

7 UDI-DI variants

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Applied filters

basicUdiUlid01JTN8W2RH8GYJKFA247TKADN4

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

MEDORA 2 Basic05904183219578
MEDORA 3 Basic05904183219561
MEDORA 3 Plus05904183219554
MEDORA 5 Pro+05904183219516
MEDORA Basic05904183219547
MEDORA Plus05904183219530
MEDORA Pro05904183219523