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PORTUX CAD/CAM Disc. 98.5X 25mm C2. MN

FDA UDI

Class II (US FDA UDI)

by Productora Y Comercializadora Odontologica New Stetic S A

Identity

Trade Name
PORTUX CAD/CAM Disc. 98.5X 25mm C2. MN FDA UDI
Generic Name
Temporary dental crown/bridge resin FDA UDI
Device Name
PORTUX CAD/CAM Disc. 98.5X 25mm C2. MN FDA UDI
Model / Reference
0023326 FDA UDI
Description
PORTUX CAD/CAM Disc. 98.5X 25mm C2. MN FDA UDI

Identifiers

Catalog Number
0023326 FDA UDI
Primary DI / UDI-DI
07701126712305 FDA UDI
510(k) Number
K192153 FDA UDI
FDA Product Code
EBG FDA UDI
GMDN Term
Temporary dental crown/bridge resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3770 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Temporary dental crown/bridge resin

PORTUX CAD/CAM Disc. 98.5X 25mm C2. MN by Productora Y Comercializadora Odontologica New Stetic S A — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Temporary dental crown/bridge resin.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 860c3a4a-1928-4a0d-8a75-f314bb86956e 35 fields · synced May 31, 2026