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Maxfill+ - Nano Hi̇bri̇t - C2 Nano Hi̇bri̇t Kompozi̇t Di̇ş Dolgusu

by Fsm Dental Medi̇kal Maki̇na Sanayi̇ Ve Ti̇caret Li̇mi̇ted Şi̇rketi̇

Ref NF010319C2(1000)Model MAXFILL+ C2 NANO HİBRİT KOMPOZİT DİŞ DOLGUSU

Active European Union

CE MDD

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08682118190891 Basic UDI-DI 08682118190891UDI-DIDate29 Apr 2026RegisteredStatusActive

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

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Model / Reference
MAXFILL+ C2 NANO HİBRİT KOMPOZİT DİŞ DOLGUSU, NF010319C2(1000)
Primary DI / UDI-DI
08682118190891
Basic UDI-DI
B-08682118190891
EMDN Code
Q01010103 Dental restorative composites
Device Class
Class IIa
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000017766

Other devices from Fsm Dental Medi̇kal Maki̇na Sanayi̇ Ve Ti̇caret Li̇mi̇ted Şi̇rketi̇

Properties

Other properties (13)

  • Sterile: No
  • Implantable: 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