Identity
- Trade Name
- Erkoloc-pro 240 EUDAMED
- Device Name
- Erkoloc-pro, 1,00 mm, Ø 120 mm, transparent EUDAMED
- Model / Reference
- Erkoloc-pro EUDAMED599510 EUDAMED
Identifiers
- Primary DI / UDI-DI
- +ERKO5995101 EUDAMED
- Basic UDI-DI
- ++ERKO052aNNNNN1209T8 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
Erkoloc-pro 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | ++ERKO052aNNNNN1209T8 | Class IIa | Active |
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Manufacturer
- Manufacturer
- Erkodent Erich Kopp GmbH
- EUDAMED SRN
- DE-MF-000006243
Sources (1)
- EUDAMED 2c19a23e-200b-4230-a786-03baa5d16d56 61 fields · synced Jul 9, 2026