| Primary Device ID | 00851067007019 |
| NIH Device Record Key | a3ee661a-7b79-4ad2-96eb-c2bb2c534630 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SuniRay2 |
| Version Model Number | Sensor #1 size |
| Catalog Number | 400-1226-B |
| Company DUNS | 180451106 |
| Company Name | SUNI MEDICAL IMAGING, INC. |
| 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 | false |
| 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 |