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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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Taboret do badania pacjentów / Patient… — 6 UDI-DI variants, MDR

MD Atlas
FAMED ŻYWIEC SP. Z O.O.

Data from EUDAMED, last updated May 31, 2026

Taboret do badania pacjentów / Patient examination stool

59041572AM204BX

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: FAMED ŻYWIEC SP. Z O.O.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 59041572AM204BX
Device name: Taboret do badania pacjentów / Patient examination stool
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 11, 2025

Manufacturer & authorised representative

Manufacturer

Name: FAMED ŻYWIEC SP. Z O.O.
SRN: PL-MF-000002794
Country: Poland
Email: sekretariat@famed.com.pl
Phone: +48 33 866 62 00

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01K2CK2BZGCCV6WVDTSM7R11QW

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

Patient examination stool05904157208867
Patient examination stool05904157208874
Patient examination stool05904157208898
Patient examination stool05904157208850
Patient examination stool05904157208843
Patient examination stool05904157208881