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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

LEVEL FIRM DM — Class I MDR by IL MATERASSAIO S.R.L.

MD Atlas
IL MATERASSAIO S.R.L.

EUDAMED last updated this device on Apr 20, 2026

LEVEL FIRM DM

805750602MEMORYEY

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: IL MATERASSAIO S.R.L.
UDI-DI code: 08057506020201
Reference / catalog number: LEVEL FIRM DM

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View device family (Basic UDI)

Manufacturer information

Organization name: IL MATERASSAIO S.R.L.
SRN: IT-MF-000021068
Manufacturer status: Active

Related devices

ANTARES DM805750602MEMORYEYOn the market ANTIDEC 32805750602MEMORYEYOn the market ANTIDEC76805750602MEMORYEYOn the market ANTIDEC 97805750602MEMORYEYOn the market ANTIDEC ALDO805750602MOLLED3On 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.

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08057506020201
Basic UDI-DI: 805750602MEMORYEY
Reference / catalog number: LEVEL FIRM DM
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: Non ci sono particolari indicazioni da seguire relativamente alla conservazione del materasso; tuttavia, si raccomanda in caso di prolungata inutilizzazione di non conservare il materasso piegandolo o comprimendolo. Tutte le lastre dei prodotti potranno subire variazioni cromatiche per specifiche esigenze produttive; si sottolinea che tali variazioni non inficeranno in modo alcuno le caratteristiche tecniche e prestazionali del prodotto stesso.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08057506020201

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

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

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