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Abformlöffel OK 4 S Full Denture perforiert

EUDAMED

Class I (EU MDR)

Ref 314Model KKD Abformlöffel

by Kentzler-Kaschner Dental GmbH

Identity

Trade Name
Abformlöffel OK 4 S Full Denture perforiert EUDAMED
Model / Reference
KKD Abformlöffel EUDAMED
314 EUDAMED

Identifiers

Primary DI / UDI-DI
+EKKD3141 EUDAMED
Basic UDI-DI
++EKKDABFORMLOEFFELJT EUDAMED
EMDN Code
Q010207 DENTAL IMPRESSION DEVICES FOR PROSTHETIC DENTISTRY EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

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

Category: Dental implant suprastructure, temporary, preformed, single-use

Abformlöffel OK 4 S Full Denture perforiert by Kentzler-Kaschner Dental GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, temporary, preformed, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
DE-MF-000006366

Sources (1)

  • EUDAMED e551e101-c4cd-4931-95d7-350c391d22e6 61 fields · synced Jun 19, 2026