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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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NYAKORTÉZISEK — 9 UDI-DI variants, MDR

MD Atlas
PATELLA-96 Kereskedelmi és Szolgáltató Korlátolt Felelősségű Társaság

Data from EUDAMED, last updated May 24, 2026

NYAKORTÉZISEK

599954297GM0932QK

9 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-96 Kereskedelmi és Szolgáltató Korlátolt Felelősségű Társaság

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 599954297GM0932QK
Device name: NYAKORTÉZISEK
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 25, 2022

Manufacturer & authorised representative

Manufacturer

Name: PATELLA-96 Kereskedelmi és Szolgáltató Korlátolt Felelősségű Társaság
SRN: HU-MF-000004588
Country: Hungary
Email: info@patella.hu

Variants by status

UDI-DI variants

9 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FWRHA3NZE573QHHSRYSMXYRP

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

GM-C4 L05999542973420
GM-C4 M05999542972423
GM-C4 S05999542970429
GM-C6 L05999542970405
GM-C6 M05999542970399
GMED-C3 L05999542973413
GMED-C3 M05999542972416
GMED-C3 S05999542970412
GMED-C3 XL05999542973406