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Komobì
EUDAMEDClass I (EU MDR)
Ref 332800Model 332420, 332470, 332480, 332490, 332800, 332820, 332840
Identity
- Trade Name
- KOMOBì EUDAMED
- Device Name
- KOMOBì EUDAMED
- Model / Reference
- 332420, 332470, 332480, 332490, 332800, 332820, 332840 EUDAMED332800 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08058302601557 EUDAMED
- Basic UDI-DI
- 805830260KOMOBIDX EUDAMED
- Direct Marketing DI
- 08058302601557 EUDAMED
- EMDN Code
- Y1803 ASSISTIVE TABLES EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Italy EUDAMED
Clinical & Handling
Sterile
No
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
Komobì by Malvestio Spa — 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 | 805830260KOMOBIDX | Class I | Active |
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Manufacturer
- Manufacturer
- Malvestio Spa
- EUDAMED SRN
- IT-MF-000013307
Sources (1)
- EUDAMED 8824d6b6-bb48-4345-bf52-b92bed8f8590 61 fields · synced Sep 18, 2026