Identity
- Device Name
- ALFADEK EUDAMED
- Model / Reference
- ALFADEK 18/09 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08056479540044 EUDAMED
- Basic UDI-DI
- B-08056479540044 EUDAMED
- EMDN Code
- Z121301 PERCUTANEOUS DISCECTOMY EQUIPMENT EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Italy EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Alfadek by Alfamed Srl — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-08056479540044 | Class IIa | Active |
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Manufacturer
- Manufacturer
- Alfamed Srl
- EUDAMED SRN
- IT-MF-000033580
Sources (1)
- EUDAMED ae17f07b-348f-4718-898f-79f182ea9700 61 fields · synced Jun 20, 2026