| Primary Device ID | 00812432021306 |
| NIH Device Record Key | ede814b2-9bee-4af7-81a6-b7bbfc24088a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Precision Spine Midline Cortical Surgical Illuminator |
| Version Model Number | 011652 |
| Catalog Number | 59-LS-5000 |
| Company DUNS | 108631797 |
| Company Name | LUMITEX, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |