| Primary Device ID | 07290117771921 |
| NIH Device Record Key | f49eaea5-6970-4e3f-99b8-85437c660a25 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | OptiLight Filter |
| Version Model Number | NA |
| Company DUNS | 600763501 |
| Company Name | LUMENIS BE LTD |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07290117771921 [Primary] |
| QIU | Intense Pulsed Light Device For Managing Dry Eye |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-03-29 |
| Device Publish Date | 2023-03-21 |
| 07290117772447 - FoLiCool™ Tip | 2024-03-25 |
| 07290117772522 - FoLix™ | 2024-03-25 |
| 07290117772539 - FoLix™ Handpiece | 2024-03-25 |
| 07290117772393 - LUSTER System | 2024-01-30 |
| 07290117772409 - LUSTER Handpiece | 2024-01-30 |
| 07290117772416 - LUSTER Tip, Round | 2024-01-30 |
| 17290117772420 - OPT™ Shields | 2024-01-03 |
| 07290117771372 - AcuPulse | 2023-12-12 |