Identity
- Trade Name
- Bella Lumax rotative double intensité EUDAMED
- Device Name
- BELLA LUMAX EUDAMED
- Model / Reference
- LED22650R-DI EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03760361831435 EUDAMED
- Basic UDI-DI
- 376036183LUMAXF6 EUDAMED
- EMDN Code
- Z12010702 MOBILE SCIALYTIC LAMPS EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- France 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
Bella Lumax rotative double intensité by Lid - Sotramet — 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 | 376036183LUMAXF6 | Class I | Active |
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Manufacturer
- Manufacturer
- Lid - Sotramet
- EUDAMED SRN
- FR-MF-000014659
Sources (1)
- EUDAMED f5d2a95b-e7ca-484d-96df-90aa5ea1e1ff 61 fields · synced Jul 12, 2026