| Primary Device ID | 04582667985648 |
| NIH Device Record Key | d9e61659-2f14-4585-8ed6-3019c454d7cc |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | EYEVAN7285 |
| Version Model Number | 170 49 800-G DK.BR |
| Company DUNS | 705184505 |
| Company Name | EYEVAN 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 | false |
| Lot Batch | false |
| 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 |