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Dehp

EUDAMED

Class IIa (EU MDR)

Ref 9796470Model TF-080 (DEHP)

by CB Healthcare Consulting GmbH

Identity

Trade Name
DEHP EUDAMED
Device Name
Zinkoxid Eugenol Cement EUDAMED
Model / Reference
TF-080 (DEHP) EUDAMED
9796470 EUDAMED

Identifiers

Primary DI / UDI-DI
04062183033691 EUDAMED
Basic UDI-DI
B-04062183033691 EUDAMED
EMDN Code
Q01010299 ROOT CANAL FILLING DEVICES - 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

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Dehp by CB Healthcare Consulting GmbH — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
DE-MF-000005902

Sources (1)

  • EUDAMED 2e78055c-48a3-461f-8ede-ce5559dc0ded 61 fields · synced Oct 5, 2026