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Bende premifistola coesive
EUDAMEDClass I (EU MDR)
Ref DR 10-2AModel Dispositivi PremifistolaRef DR 10-60ARef DR 10-2A-10
Identity
- Trade Name
- Bende premifistola coesive EUDAMED
- Device Name
- Bende Premifistola EUDAMED
- Model / Reference
- Dispositivi Premifistola EUDAMEDDR 10-2A EUDAMEDDR 10-60A EUDAMEDDR 10-2A-10 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08059591521946 EUDAMED08059591522387 EUDAMED08059591522011 EUDAMED
- Basic UDI-DI
- 805959152PREMN4 EUDAMED
- EMDN Code
- M030404 DIALYSIS FISTULA, BANDAGES 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
Bende premifistola coesive by D.r.m. S.r.l. — 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 | 805959152PREMN4 | Class I | Active |
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Manufacturer
- Manufacturer
- D.r.m. S.r.l.
- EUDAMED SRN
- IT-MF-000027115
Sources (3)
- EUDAMED 1ce672a3-0305-4226-89bf-5730ffc8d32d 61 fields · synced Sep 18, 2026
- EUDAMED ccad701e-5adf-477f-8c88-e70c054dfe78 61 fields · synced May 17, 2026
- EUDAMED 2bbbb033-58ec-4918-8485-7969c4e94d22 61 fields · synced May 18, 2026