Identity
- Trade Name
- ASSUPRO EUDAMED
- Device Name
- ASSUPRO EUDAMED
- Model / Reference
- PV516AH EUDAMED
Identifiers
- Primary DI / UDI-DI
- 38033439437317 EUDAMED
- Basic UDI-DI
- 8033439ASSUPRO4P EUDAMED
- Direct Marketing DI
- 38033439437317 EUDAMED
- EMDN Code
- H010201010401 POLYPROPYLENE MONOFILAMENT WITH NEEDLE FOR OPEN SURGERY EUDAMED
Classification
- Device Class
- Class III EUDAMED
- Market of Registration
- Italy EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
Yes
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
Assupro by Assut Europe Spa — Class III — 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 | 8033439ASSUPRO4P | Class III | Active |
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Manufacturer
- Manufacturer
- Assut Europe Spa
- EUDAMED SRN
- IT-MF-000018178
Sources (1)
- EUDAMED 20f386d5-d989-49fd-84df-5b95625c481a 61 fields · synced Aug 1, 2026