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Organization name
UDI-DI code
Reference / catalog number

3000219240 — Class I MDR by NEVEON Austria GmbH

MD Atlas
NEVEON Austria GmbH

EUDAMED last updated this device on Aug 2, 2023

3000219240

9006399DekuTrioUnitS9

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: NEVEON Austria GmbH
UDI-DI code: 09006399000066
Reference / catalog number: 3000219240

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Manufacturer information

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

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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 2 countries total.

Country	On market since	Until
AustriaPrimary placement	Mar 1, 2021	Still on market
Germany	Mar 1, 2021	Still on market

Device identification

Trade name: not provided
UDI-DI code: 09006399000066
Basic UDI-DI: 9006399DekuTrioUnitS9
Reference / catalog number: 3000219240
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: Large Wedge - part of Deku Trio set Size: 800 x 320 x 140/1 mm, cover PU-210, AntiSlip This one-sided anti-decubitus mattress is ideal for patients at risk of bedsores as well as for allergy sufferers. It can be used in hospitals, retirement and nursing homes, rehabilitation centers, home care situations and palliative care. A wide range of positioning techniques can be practiced in line with the latest patient care advice with very little need to use aids.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V0880MEDICAL SUPPORT EQUIPMENT - ACCESSORIES

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

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