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Erkodur 240

EUDAMED

Class IIa (EU MDR)

Ref 529510Model ErkodurRef 529508Ref 529506

by Erkodent Erich Kopp GmbH

Identity

Trade Name
Erkodur 240 EUDAMED
Device Name
Erkodur, 1,00 mm, Ø 120 mm, klar EUDAMED
Model / Reference
Erkodur EUDAMED
529510 EUDAMED
529508 EUDAMED
529506 EUDAMED

Identifiers

Primary DI / UDI-DI
+ERKO5295101 EUDAMED
+ERKO5295081 EUDAMED
+ERKO5295061 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 240 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 (3)

  • EUDAMED eca3f672-aefd-4446-8a07-ea8671f7e623 61 fields · synced Jul 9, 2026
  • EUDAMED 6a45a7e8-a8dc-4359-8484-339f01a9bedf 61 fields · synced May 17, 2026
  • EUDAMED b10e0b34-ce55-4919-aef2-c0977fbb7ee6 61 fields · synced May 18, 2026