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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 previcrepe — 55 UDI-DI variants, MDR (Medinovitas Kft)

MD Atlas
Medinovitas Kft

Data from EUDAMED, last updated May 24, 2026

Benda elastica previcrepe

599957142M0303010101Z5

55 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: 599957142M0303010101Z5
Device name: Benda elastica previcrepe
Device model: Benda elastica previcrepe
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 15, 2024

Manufacturer & authorised representative

Manufacturer

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

Variants by status

UDI-DI variants

55 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J2TRP197DPMGA0QE0QWNASF8

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

LAS0400805999571422043
LAS04010105999571422081
LAS04004105999571421992
LAS04006105999571422029
LAS04008105999571422050

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