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Constella
EUDAMEDClass I (EU MDR)
Ref LF90275/CONSTELLA-D(M)Model Celesta & Luminox
Identity
- Trade Name
- CONSTELLA EUDAMED
- Device Name
- Celesta & Luminox EUDAMED
- Model / Reference
- Celesta & Luminox EUDAMEDLF90275/CONSTELLA-D(M) EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08906164080600 EUDAMED
- Basic UDI-DI
- 890616408OTLRF EUDAMED
- EMDN Code
- Z12010702 MOBILE SCIALYTIC LAMPS EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Germany 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
Constella by Eclipse Prism Medical Devices Private Limited — 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 | 890616408OTLRF | Class I | Active |
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Manufacturer
- Manufacturer
- Eclipse Prism Medical Devices Private Limited
- EUDAMED SRN
- IN-MF-000032926
- Authorised Representative
- Mars Medical DE-AR-000006312
Sources (1)
- EUDAMED 82679f75-bba5-4b5e-8979-522eb333ba01 61 fields · synced Jun 19, 2026