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Bifluorid 10

EUDAMED

Class IIa (EU MDR)

Ref 1616Model Bottle

by VOCO GmbH

Identity

Trade Name
Bifluorid 10 EUDAMED
Device Name
Bifluorid 10 EUDAMED
Model / Reference
Bottle EUDAMED
1616 EUDAMED

Identifiers

Primary DI / UDI-DI
E22116161 EUDAMED
Basic UDI-DI
B-E22116161 EUDAMED
EMDN Code
Q0101010299 TEMPORARY AND PERMANENT DENTAL RESTORATION CEMENTS - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

Yes

EUDAMED

Category: Dental composite resin

Bifluorid 10 by VOCO GmbH — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental composite resin.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
VOCO GmbH
EUDAMED SRN
DE-MF-000008601

Sources (1)

  • EUDAMED bed32e8b-c710-4a11-8964-03731b40e6bd 61 fields · synced Jun 18, 2026