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Portux 3D Printing Resin Cast

FDA UDI

Class I (US FDA UDI)

by Productora Y Comercializadora Odontologica New Stetic S A

Identity

Trade Name
Portux 3D Printing Resin Cast FDA UDI
Generic Name
Dental appliance fabrication material, ceramic FDA UDI
Device Name
Portux 3D Printing Resin Cast x 500g FDA UDI
Model / Reference
0028439 FDA UDI
Description
Portux 3D Printing Resin Cast x 500g FDA UDI

Identifiers

Catalog Number
0028439 FDA UDI
Primary DI / UDI-DI
07701126901150 FDA UDI
FDA Product Code
EGD FDA UDI
GMDN Term
Dental appliance fabrication material, ceramic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6890 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Portux 3D Printing Resin Cast by Productora Y Comercializadora Odontologica New Stetic S A — Class I — FDA UDI — listed in FDA GUDID

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 22e5e8a9-3e10-4231-94b3-06d52ab2c14b 35 fields · synced Jun 8, 2026