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Erkodur

EUDAMED

Class IIa (EU MDR)

Ref 521210Model Erkodur

by Erkodent Erich Kopp GmbH

Identity

Trade Name
Erkodur EUDAMED
Device Name
Erkodur, 1,00 mm, Ø 120 mm, klar EUDAMED
Model / Reference
Erkodur EUDAMED
521210 EUDAMED

Identifiers

Primary DI / UDI-DI
+ERKO5212101 EUDAMED
Basic UDI-DI
++ERKO022aNNNNN1209PR EUDAMED
Unit of Use DI
1 EUDAMED
EMDN Code
Q010699 MATERIALS FOR THE PREPARATION OF CUSTOM-MADE DENTAL DEVICES - OTHER EUDAMED

Classification

Device Class
Class IIa 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

Erkodur by Erkodent Erich Kopp Gmbh — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
DE-MF-000006243

Sources (1)

  • EUDAMED e816b317-1438-4177-981f-ab787a021677 61 fields · synced May 29, 2026