| Primary Device ID | 03760310780258 |
| NIH Device Record Key | 0108b612-3509-4623-a16f-44e15c5d405b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | HemiNeglect |
| Version Model Number | v1.3.7 |
| Company DUNS | 267153884 |
| Company Name | VIRTUALIS |
| 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 |