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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

SI5022.280 — Class I MDR by Stiloptic di Celer…

MD Atlas
Stiloptic di Celer Patrycja Ewa

EUDAMED last updated this device on Apr 29, 2026

SI5022.280

805415467AQ02100202CR

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Stiloptic di Celer Patrycja Ewa
UDI-DI code: 80541546750364
Reference / catalog number: SI5022.280

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View device family (Basic UDI)

Manufacturer information

Organization name: Stiloptic di Celer Patrycja Ewa
SRN: IT-MF-000027197
Manufacturer status: Active

Related devices

SI5011.124805415467AQ02100202CROn the market SI5011.133805415467AQ02100202CROn the market SI5011.145805415467AQ02100202CROn the market SI5011.176805415467AQ02100202CROn the market SI5019.257805415467AQ02100202CROn 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: 80541546750364
Basic UDI-DI: 805415467AQ02100202CR
Reference / catalog number: SI5022.280
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: 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)80541546750364

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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.

Q02100202PLASTIC SPECTACLE FRAMES WITHOUT LENSES

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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