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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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Próżniowy system pozycjonujący do… — 2 UDI-DI variants, MDR

MD Atlas
Noel Zebrowski sp.j

Data from EUDAMED, last updated May 31, 2026

Próżniowy system pozycjonujący do stabilizacji tułowia, kończyn i głowy, podłokietnik ARMREST VELCRO

5902596723Armrest2K

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: Noel Zebrowski sp.j

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5902596723Armrest2K
Device name: Próżniowy system pozycjonujący do stabilizacji tułowia, kończyn i głowy, podłokietnik ARMREST VELCRO
Device model: ARMREST VELCRO M
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 18, 2026

Manufacturer & authorised representative

Manufacturer

Name: Noel Zebrowski sp.j
SRN: PL-MF-000002986
Country: Poland
Email: stabilo@stabilo.krakow.pl
Phone: +48 123415316

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KHRBCA27A6SCN85G84D3D8PD

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

2991262/V05902596723538
2991261/V05902596723521