Luminox
by Eclipse Prism Medical Devices Private Limited 23 variants
Ref LF90185/LSDDFF01B/CModel Celesta & Luminox
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number890616408OTLRF 08906164080099 | Date24 Jan 2023 | StatusActive |
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Celesta & Luminox
- Model / Reference
- Celesta & Luminox, LF90185/LSDDFF01B/C
- Primary DI / UDI-DI
- 08906164080099
- Basic UDI-DI
- 890616408OTLRF
- Direct Marketing DI
- 08906164080099
- EMDN Code
- Z12010701 Fixed scialytic lamps
- Device Class
- Class I
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- IN-MF-000032926
- Authorised representative
- Mars Medical DE-AR-000006312
Other devices from Eclipse Prism Medical Devices Private Limited
See all devices from Eclipse Prism Medical Devices Private Limited →
Properties
Other properties (13)
- Sterile: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No