Identity
- Device Name
- Applicatore uretrale EUDAMED
- Model / Reference
- 02452101 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08015262036249 EUDAMED
- Basic UDI-DI
- 80152621114R EUDAMED
- EMDN Code
- U03010201 URETHRAL DILATORS EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Italy EUDAMED
Clinical & Handling
Sterile
Yes
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
Applicatore uretrale by Pentaferte Italia Srl — 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 | 80152621114R | Class I | Active |
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Manufacturer
- Manufacturer
- Pentaferte Italia Srl
- EUDAMED SRN
- IT-MF-000040982
Sources (1)
- EUDAMED 645686a2-c0ab-4c78-9b56-5d2df3634b62 61 fields · synced Jun 19, 2026