FLUOBEAM LS system
Ref CS_FBLS_DU
FLUOBEAM LS system (CS_FBLS_DU) is a Class IIa device made by Fluoptics SAS, registered in EUDAMED on 21 Oct 2024 (Basic UDI-DI ++B475CSFBLSXQ), active as of 23 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number++B475CSFBLSXQ +B475CSFBLSDU0 | Date21 Oct 2024 | StatusActive |
Official records
- EUDAMED public site ++B475CSFBLSXQ
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device name
- FLUOBEAM LS system
- Model / reference
- CS_FBLS_DU
- Primary DI / UDI-DI
- +B475CSFBLSDU0
- Basic UDI-DI
- ++B475CSFBLSXQ
- EMDN code
- Z119080 Various bioimaging and radiotherapy instruments - hardware accessories
- Device class
- Class IIa
- System or procedure pack
- System
- EU registration type
- System or procedure pack
- Medical purpose
- FLUOBEAM LS including FLUOSOFT LS is indicated to facilitate the visualization of parathyroid glands by auto-fluorescence (natural fluorescence without ICG injection) during thyroid and parathyroid surgeries. FLUOBEAM LS including FLUOSOFT LS is indicated to visualize on a screen the flow, the distribution and/ or the accumulation of Indocyanine green (ICG) before, during and after surgery for the indications such as: • visualization of blood flow, vessels and tissue perfusion • visualization of lymphatic system, including lymph node and vessels • visualization of malignant tissues
Manufacturer details
- EUDAMED SRN
- FR-PR-000002882
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