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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

31014 — Class I MDR by S.I.Cell S.p.A.

MD Atlas
S.I.Cell S.p.A.

EUDAMED last updated this device on Apr 17, 2026

31014

805614960SHAPEDDIAPERX7

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: S.I.Cell S.p.A.
UDI-DI code: 08056149601150
Reference / catalog number: 31014

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View device family (Basic UDI)

Manufacturer information

Organization name: S.I.Cell S.p.A.
SRN: IT-MF-000029406
Manufacturer status: Active

Related devices

30336805614960ALLINONEDIAPERF7On the market 30335805614960ALLINONEDIAPERF7On the market 31016805614960SHAPEDDIAPERX7On the market 31017805614960SHAPEDDIAPERX7On the market 31015805614960SHAPEDDIAPERX7On 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: 08056149601150
Basic UDI-DI: 805614960SHAPEDDIAPERX7
Reference / catalog number: 31014
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: 20
Additional product description: —
Additional information URL: https://www.sicell.it/
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)08056149601150

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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.

T04010102SHAPED INCONTINENCE NAPPIES

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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