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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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GYERMEKPELENKA — 4 UDI-DI variants, MDR

MD Atlas
Patella Medical Korlátolt Felelősségű Társaság

Data from EUDAMED, last updated May 24, 2026

GYERMEKPELENKA

599954297GYP38

4 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: Patella Medical Korlátolt Felelősségű Társaság

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 599954297GYP38
Device name: GYERMEKPELENKA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 1, 2025

Manufacturer & authorised representative

Manufacturer

Name: Patella Medical Korlátolt Felelősségű Társaság
SRN: HU-MF-000005868
Country: Hungary
Email: lilla.vincze@patella.hu

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K6FSHXPFM8WVW4H7SW7JTW59

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

599954297901905999542979019
599954297408305999542974083
599954297406905999542974069
599954297407605999542974076