Identity
- Device Name
- Abformpfosten EUDAMED
- Model / Reference
- Abformpfosten EUDAMED23.260.38.011 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04251923109394 EUDAMED
- Basic UDI-DI
- 4251923112615181321147LU 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
Abformpfosten by Heliocos GmbH — Class I — 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 | 4251923112615181321147LU | Class I | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Heliocos GmbH
- EUDAMED SRN
- DE-MF-000006272
Sources (1)
- EUDAMED cbae1389-f24f-4cdc-b7b1-d2072656bccd 61 fields · synced Oct 5, 2026