Allcem Veneer APS

FDA UDI

Class II (US FDA UDI)

by Dentscare Ltda

Identity

Trade Name: Allcem Veneer APS FDA UDI
Generic Name: Dental composite resin FDA UDI
Device Name: Allcem Veneer APS Mini Kit. FDA UDI
Model / Reference: Mini Kit FDA UDI
Description: Allcem Veneer APS Mini Kit. FDA UDI

Identifiers

Catalog Number: 4000019297 FDA UDI
Primary DI / UDI-DI: 07899633816552 FDA UDI
FDA Product Code: EBF FDA UDI
KLE FDA UDI
GMDN Term: Dental composite resin FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 872.3690 FDA UDI
872.3200 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental composite resin Dentine bonding agent/set Dentifrice

Allcem Veneer APS by Dentscare Ltda — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Dentscare Ltda

Sources (1)

FDA UDI f2fca625-7dea-48b2-ad0c-ce1bd15a259b 34 fields · synced Jun 6, 2026