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Portux®

EUDAMED

Class IIa (EU MDR)

Ref 0024482 CEModel PMMA MULTI DISC WITH SHOULDER 98.5X18mm 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 MULTI DISC WITH SHOULDER 98.5X18mm D2 EUDAMED
0024482 CE EUDAMED

Identifiers

Primary DI / UDI-DI
07701126713074 EUDAMED
Basic UDI-DI
7701126713074WT 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 9c47dbc8-6a0e-4d3d-a406-44177d8ef76b 61 fields · synced Oct 7, 2026