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Cerotto premifistola
EUDAMEDClass I (EU MDR)
Ref DR 25/15Model Dispositivi Premifistola
Identity
- Trade Name
- Cerotto premifistola EUDAMED
- Device Name
- Bende Premifistola EUDAMED
- Model / Reference
- Dispositivi Premifistola EUDAMEDDR 25/15 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08059591523520 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
Cerotto 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 (1)
- EUDAMED 62897230-d13a-4f31-adf6-760ec6f3e8f6 61 fields · synced Jul 25, 2026