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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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Stolik przyłóżkowy ERGO / Bedside… — 2 UDI-DI variants, MDR

MD Atlas
FAMED ŻYWIEC SP. Z O.O.

Data from EUDAMED, last updated May 30, 2026

Stolik przyłóżkowy ERGO / Bedside table ERGO

59041572ERGOPY

2 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: 59041572ERGOPY
Device name: Stolik przyłóżkowy ERGO / Bedside table ERGO
Device model: ERGO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 22, 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

2 UDI-DI variants

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Applied filters

basicUdiUlid01K38VCVMGGDAS3ZFS7R6KYYH2

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

Bedside table ERGO05904157208959
Bedside table ERGO05904157208942