Identity
- Trade Name
- CoMoveIT Flex dF EUDAMED
- Device Name
- CoMoveIT Flex EUDAMED
- Model / Reference
- CoMoveIT Flex dF EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05430002911137 EUDAMED
- Basic UDI-DI
- 5430002911CMFLEXP2 EUDAMED
- Direct Marketing DI
- 05430002911137 EUDAMED
- EMDN Code
- Y122403 WHEELCHAIR FOOTRESTS, SUPPORTS AND CONTROLS EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Belgium 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
CoMoveIT Flex dF by Comoveit — 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 | 5430002911CMFLEXP2 | Class I | Active |
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Manufacturer
- Manufacturer
- CoMoveIT
- EUDAMED SRN
- BE-MF-000017867
Sources (1)
- EUDAMED 41f728d7-ba75-4b69-8f63-00e0c8aa9846 61 fields · synced Aug 3, 2026