← Back to catalogue

PMMA CAD/CAM disc

FDA UDI

Class II (US FDA UDI)

by POLIDENT d.o.o.

Identity

Trade Name
PMMA CAD/CAM disc FDA UDI
Generic Name
Resin artificial teeth FDA UDI
Device Name
"PMMA CAD/CAM disc B3-20-98,5-SHOULDER MULTILAYER" FDA UDI
Model / Reference
PMMAML.335 FDA UDI
Description
"PMMA CAD/CAM disc B3-20-98,5-SHOULDER MULTILAYER" FDA UDI

Identifiers

Catalog Number
PMMAML.335 FDA UDI
Primary DI / UDI-DI
EPOLPMMAML3350 FDA UDI
FDA Product Code
EBG FDA UDI
ELM FDA UDI
GMDN Term
Resin artificial teeth FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3770 FDA UDI
872.3590 FDA UDI
Commercial Distribution
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

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

No

FDA UDI

Category: Resin artificial teethTemporary dental crown/bridge

PMMA CAD/CAM disc by POLIDENT d.o.o. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Temporary dental crown/bridge.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
POLIDENT d.o.o.

Sources (1)

  • FDA UDI 01ea3b72-d456-4d8a-a7e8-61bdb414ab42 35 fields · synced May 30, 2026