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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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Organization name
UDI-DI code
Reference / catalog number

3000406923 — Class I MDR by NEVEON Austria GmbH

MD Atlas
NEVEON Austria GmbH

EUDAMED last updated this device on Apr 17, 2026

3000406923

9006399DekuMaxWW

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: NEVEON Austria GmbH
UDI-DI code: 09006399000950
Reference / catalog number: 3000406923

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Manufacturer information

Organization name: NEVEON Austria GmbH
SRN: AT-MF-000003497
Manufacturer status: Active

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30003802449006399DekuCareGDOn the market 30002310519006399DekuCareGDOn the market 30004002939006399DekuCareGDOn the market 30003923319006399DekuCareGDOn the market 30001273919006399DekuDuoWTOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Market distribution

Primary placement in Austria; available across 1 country total.

Country	On market since	Until
AustriaPrimary placement	Apr 17, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 09006399000950
Basic UDI-DI: 9006399DekuMaxWW
Reference / catalog number: 3000406923
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V080702NON ACTIVE ANTI-DECUBITUS MEDICAL MATTRESSES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
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Software identification