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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

171278 — Class I MDR by EM.AN SRL

MD Atlas
EM.AN SRL

EUDAMED last updated this device on May 27, 2026

171278

805404029MAT78IS22EM15HU

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: EM.AN SRL
UDI-DI code: 08054040291555
Reference / catalog number: 171278

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View device family (Basic UDI)

Manufacturer information

Organization name: EM.AN SRL
SRN: IT-MF-000055216
Manufacturer status: Active

Related devices

170757805404029MAT78IS22EM15HUOn the market 170757805404029MAT78IS22EM15HUOn the market 170757805404029MAT78IS22EM15HUOn the market 171278805404029MAT78IS22EM15HUOn the market 171278805404029MAT78IS22EM15HUOn 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: 08054040291555
Basic UDI-DI: 805404029MAT78IS22EM15HU
Reference / catalog number: 171278
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: MATERASSO MEDICALE ANTIDECUBITO NON ATTIVO
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)08054040291555

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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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