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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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Deku Max — 16 UDI-DI variants, MDR (NEVEON Austria GmbH)

MD Atlas
NEVEON Austria GmbH

Data from EUDAMED, last updated May 23, 2026

Deku Max

9006399DekuMaxWW

16 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: NEVEON Austria GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 9006399DekuMaxWW
Device name: Deku Max
Device model: Deku Max
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 6, 2023

Manufacturer & authorised representative

Manufacturer

Name: NEVEON Austria GmbH
SRN: AT-MF-000003497
Country: Austria
Email: office@neveon.com

Variants by status

UDI-DI variants

16 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HGZT1QM16H5YEDH5DW2DASAH

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

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300035904709006399000424
300038085809006399000974
300004990509006399000998
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300040128109006399000882
300040692309006399000950
300032836209006399000271
300006810309006399000981
300038127109006399000677
300039334309006399000806
300021923309006399001315
300017297109006399006341
300001396009006399001148