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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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LYSONOX DECON FX — 4 UDI-DI variants, MDR (ADRANOX SRL)

MD Atlas
ADRANOX SRL

Data from EUDAMED, last updated May 30, 2026

LYSONOX DECON FX

805630441LYSONOXDECONFXM4

4 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: ADRANOX SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805630441LYSONOXDECONFXM4
Device name: LYSONOX DECON FX
Device model: ADWD300.50
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Nov 29, 2024

Manufacturer & authorised representative

Manufacturer

Name: ADRANOX SRL
SRN: IT-MF-000027181
Country: Italy
Email: adranox@adranox.com
Phone: +390376405362

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01JDWYSXMY8RSBRGYRQ0Y5VHA6

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

ADWD300.10008056304411181
ADWD300.25008056304411198
ADWD300.5008056304411150
ADWD300.5108056304411174