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Cerotti premifistola
EUDAMEDClass I (EU MDR)
Ref DR 20/27Model Dispositivi PremifistolaRef DR 20/25
Identity
- Trade Name
- Cerotti premifistola EUDAMED
- Device Name
- Bende Premifistola EUDAMED
- Model / Reference
- Dispositivi Premifistola EUDAMEDDR 20/27 EUDAMEDDR 20/25 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08059591527023 EUDAMED08059591522516 EUDAMED
- Basic UDI-DI
- 805959152PREMN4 EUDAMED
- EMDN Code
- M0599 MEDICAL PLASTERS - OTHER 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
Cerotti premifistola 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 (2)
- EUDAMED 96c47cf6-876b-4bb6-a99e-da11bfe11ea5 61 fields · synced Jul 17, 2026
- EUDAMED bd0140ad-2ed2-439d-a6ee-6983cfc6f669 61 fields · synced May 17, 2026