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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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Łóżko rehabilitacyjne LP-02.1 /… — 1 UDI-DI variant, MDR

MD Atlas
FAMED ŻYWIEC SP. Z O.O.

Data from EUDAMED, last updated May 30, 2026

Łóżko rehabilitacyjne LP-02.1 / Rehabilitation bed LP-02.1

59041572LP00M9

1 UDI-DI variant

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: 59041572LP00M9
Device name: Łóżko rehabilitacyjne LP-02.1 / Rehabilitation bed LP-02.1
Device model: LP-02.1
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 21, 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

1 UDI-DI variant

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Applied filters

basicUdiUlid01K36C962Y755ASYMYJMGWHJHZ

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

Rehabilitation bed LP-02.105904157204005