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Plastor

by Ghimas S.p.A. Italy EUDAMED

Ref Plastor/Dentiline EMDN Q0101010203

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-CEMENTPROVV04WU Basic UDI-DIDate16 Jan 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Plastor / Dentiline
Model / Reference
Plastor/Dentiline
Primary DI / UDI-DI
D-CEMENTPROVV04WU
Basic UDI-DI
B-CEMENTPROVV04WU
EMDN Code
Q0101010203 Temporary dental cements
Device Class
Class IIa
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000017070

Other devices from Ghimas S.p.A.

See all devices from Ghimas S.p.A. →

Properties & raw data

Show properties, registry sources and raw records
Other properties (11)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 4821749e-2ad3-4b94-aa40-ab2b809d5270 61 fields · synced 22 Oct 2026