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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

M223-SOFTPLUS — Class I MDR by Kubivent Sitz- und…

MD Atlas
Kubivent Sitz- und Liegepolster GmbH

EUDAMED last updated this device on Apr 15, 2026

M223-SOFTPLUS

42512056MatratzenADYX

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Kubivent Sitz- und Liegepolster GmbH
UDI-DI code: 04251205602629
Reference / catalog number: M223-SOFTPLUS

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Manufacturer information

Organization name: Kubivent Sitz- und Liegepolster GmbH
SRN: DE-MF-000008743
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 3 countries total.

Country	On market since	Until
GermanyPrimary placement		Still on market
Austria		Still on market
Italy		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04251205602629
Basic UDI-DI: 42512056MatratzenADYX
Reference / catalog number: M223-SOFTPLUS
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: 200x90x22 cm

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
Serial number
Software identification

Related devices

M224-SOFTPLUS42512056MatratzenADYXOn 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.