Provicol QM

FDA UDI

Class II (US FDA UDI)

by VOCO GmbH

Identity

Trade Name: Provicol QM FDA UDI
Generic Name: Fatty acid dental cement FDA UDI
Device Name: Eugenol-free temporary luting cement with calcium hydroxide. FDA UDI
Model / Reference: 1109 FDA UDI
Description: Eugenol-free temporary luting cement with calcium hydroxide. FDA UDI

Identifiers

Catalog Number: 1109 FDA UDI
Primary DI / UDI-DI: E22111091 FDA UDI
FDA Product Code: EMA FDA UDI
GMDN Term: Fatty acid dental cement FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 872.3275 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

FDA UDI

Category: Fatty acid dental cement

Provicol QM by VOCO GmbH — 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: VOCO GmbH

Sources (1)

FDA UDI 3157540a-a26f-41a7-8dbb-6e8c6130bbef 35 fields · synced May 30, 2026