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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 Duo — 6 UDI-DI variants, MDR (NEVEON Austria GmbH)

MD Atlas
NEVEON Austria GmbH

Data from EUDAMED, last updated May 23, 2026

Deku Duo

9006399DekuDuoWT

6 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: 9006399DekuDuoWT
Device name: Deku Duo
Device model: Deku Duo
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 21, 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

6 UDI-DI variants

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Applied filters

basicUdiUlid01HJ5TNX72E9J3DJ6TCWK2QKBP

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

300012739109006399000042
300014500309006399006358
300022887909006399001483
300022465909006399001476
300021053709006399001469
300012740709006399006228