Identity
- Device Name
- Core Forms EUDAMED
- Model / Reference
- HCFAP, F80690 EUDAMED
Identifiers
- Primary DI / UDI-DI
- D701HCFAP2 EUDAMED
- Basic UDI-DI
- ++D701HCFPX EUDAMED
- Unit of Use DI
- D701HCFAP1 EUDAMED
- EMDN Code
- Q01010203 DENTAL CONES EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- France 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: Synthetic gutta-percha
Core Forms by Pulpdent Corporation — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
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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 | ++D701HCFPX | Class I | Active |
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Manufacturer
- Manufacturer
- Pulpdent Corporation
- EUDAMED SRN
- US-MF-000004897
- Authorised Representative
- Advena Limited MT-AR-000000234
Sources (2)
- EUDAMED 85a4e290-32d0-4663-925c-f787739db546 61 fields · synced Jun 18, 2026
- EUDAMED 85a4e290-32d0-4663-925c-f787739db546-1 61 fields · synced Jun 10, 2026