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Portux®

by Productora Y Comercializadora Odontologica New Stetic S.a 52 variants

Ref 0023325 CEModel PMMA MONO DISC WITH SHOULDER 98.5X20mm C2

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number7701126712794XV Basic UDI-DI 07701126712794UDI-DIDate8 Jul 2025RegisteredStatusActive

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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Pmma Discs for Cad/Cam Application
Model / Reference
PMMA MONO DISC WITH SHOULDER 98.5X20mm C2, 0023325 CE
Primary DI / UDI-DI
07701126712794
Basic UDI-DI
7701126712794XV
EMDN Code
Q0102050101 Temporary teeth resins
Device Class
Class IIa
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
CO-MF-000036727
Authorised representative
Ranelagh Capital SLU ES-AR-000040175

Related devices

Category: Dental appliance fabrication material, resin

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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