DEI Clever Fibre Composite Light

by ARKONA Laboratorium Farmakologii Stomatologicznej Grzegorz Kalbarczyk

Model Light, Medium

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number590443371TF0237G Basic UDI-DI 05904433718370UDI-DI	Date11 Feb 2026Registered	StatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name: Fibre Composite / Dei Clever Fibre Composite
Model / Reference: Light, Medium

Primary DI / UDI-DI: 05904433718370
Basic UDI-DI: 590443371TF0237G
EMDN Code: Q01010103 Dental restorative composites

Device Class: Class IIa
EU market of registration: Italy

Manufacturer details

EUDAMED SRN: PL-MF-000029550

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Gąsienica zewnętrzna

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Properties

Implantable

Other properties (12)

Sterile: No
Reusable: No
Contains Latex: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No