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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

SUPERCOMFORT 2780478 — Class I MDR by TRAPUNTIFICIO C.A.T.…

MD Atlas
TRAPUNTIFICIO C.A.T. S.R.L.

EUDAMED last updated this device on Feb 23, 2026

SUPERCOMFORT 2780478

805559496MTR001NV

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: TRAPUNTIFICIO C.A.T. S.R.L.
UDI-DI code: 08055594960294
Reference / catalog number: SUPERCOMFORT 2780478

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View device family (Basic UDI)

Manufacturer information

Organization name: TRAPUNTIFICIO C.A.T. S.R.L.
SRN: IT-MF-000029712
Manufacturer status: Active

Related devices

ALIDA 2150436805559496MTR001NVOn the market ALIDA 2150436805559496MTR001NVOn the market ALIDA 2150436805559496MTR001NVOn the market BIO THERAPY 2150435805559496MTR001NVOn the market BIO THERAPY 2150435805559496MTR001NVOn the market

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Italy; available across 1 country total.

Placed on the market in Italy; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 08055594960294
Basic UDI-DI: 805559496MTR001NV
Reference / catalog number: SUPERCOMFORT 2780478
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: Double mattress in Foam and Memory Foam
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)08055594960294

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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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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.