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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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Szúnyogriasztók — 8 UDI-DI variants, MDR (Elysium Laboratories Kft.)

MD Atlas
Elysium Laboratories Kft.

Data from EUDAMED, last updated May 24, 2026

Szúnyogriasztók

5999862705RPL01UF

8 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: Elysium Laboratories Kft.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5999862705RPL01UF
Device name: Szúnyogriasztók
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 15, 2025

Manufacturer & authorised representative

Manufacturer

Name: Elysium Laboratories Kft.
SRN: HU-MF-000039543
Country: Hungary
Email: info@elysium.hu

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K2PB0VWJ67CN7YGCGD5ZTZCP

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

599986270508405999862705084
599986270509105999862705091
599986270500805999862705008
599986270502205999862705022
599986270501505999862705015
599986270503905999862705039
599986270505305999862705053
599986270504605999862705046