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Portux®

EUDAMED

Class IIa (EU MDR)

Ref 0023334 CEModel PMMA MONO DISC WITH SHOULDER 98.5X20mm D2

by Productora Y Comercializadora Odontologica New Stetic S.a

Identity

Trade Name
PORTUX® EUDAMED
Device Name
PMMA DISCS FOR CAD/CAM APPLICATION EUDAMED
Model / Reference
PMMA MONO DISC WITH SHOULDER 98.5X20mm D2 EUDAMED
0023334 CE EUDAMED

Identifiers

Primary DI / UDI-DI
07701126712831 EUDAMED
Basic UDI-DI
7701126712831XA EUDAMED
EMDN Code
Q0102050101 TEMPORARY TEETH RESINS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Dental appliance fabrication material, resin

Portux® by Productora Y Comercializadora Odontologica New Stetic S A — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental appliance fabrication material, resin.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

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

Sources (1)

  • EUDAMED abd0998e-6e64-4f5c-b12d-526b6116e622 61 fields · synced Oct 7, 2026