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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 elastica previcoesiva — 13 UDI-DI variants, MDR

MD Atlas
Medinovitas Kft

Data from EUDAMED, last updated May 24, 2026

Benda elastica previcoesiva

599957142M0303010201ZA

13 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: 599957142M0303010201ZA
Device name: Benda elastica previcoesiva
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 24, 2024

Manufacturer & authorised representative

Manufacturer

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

Variants by status

UDI-DI variants

13 UDI-DI variants

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Applied filters

basicUdiUlid01J3JKF76HV2PJWQNG8RC06QC1

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

GACO040041F05999571421671
GACO040081FL05999571421725
GACO040101FL05999571421749
GACO040101F05999571421732
GACO2001210F05999571421794
GACO040041FL05999571421688
GACO040061F05999571421695
GACO040061FL05999571421701
GACO040081F05999571421718
GACO2001010FL05999571421787
GACO2000410FL05999571421756
GACO2000610FL05999571421763
GACO2000810FL05999571421770