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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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Benda di garza — 15 UDI-DI variants, MDR (Medinovitas Kft)

MD Atlas
Medinovitas Kft

Data from EUDAMED, last updated May 24, 2026

Benda di garza

599957142M030101C9

15 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: Medinovitas Kft

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 599957142M030101C9
Device name: Benda di garza
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 1, 2024

Manufacturer & authorised representative

Manufacturer

Name: Medinovitas Kft
SRN: HU-MF-000007416
Country: Hungary
Email: amministrazione@medinovitas.eu

Variants by status

UDI-DI variants

15 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J1Q6GJCRYD3CP2RGKBP23J3B

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

20F10004105999571421213
20F10006105999571421220
23F10010105999571421275
23F100101L05999571421282
23F100151L05999571421299
23F100041L05999571421237
23F100061L05999571421244
M03010105999571421268
23F10008105999571421251
AUR100011L05999571421336
AUR10001105999571421329
AUR10002105999571421343
AUR100021L05999571421350
AUR05001105999571421305
AUR05002105999571421312