| Primary Device ID | 00859492006003 |
| NIH Device Record Key | 908bb29b-0744-43be-a92c-cabf914c8e37 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SCHOTT Universal Light Guide |
| Version Model Number | ULG-EP-4.8-3000-gy |
| Company DUNS | 601205573 |
| Company Name | SCHOTT NORTH AMERICA, INC. |
| Device Count | 1 |
| DM Exempt | true |
| 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 | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |