| Primary Device ID | 05419980275004 |
| NIH Device Record Key | 2982d4ac-3854-47db-acc5-ed8a4f62e505 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Neuroventis Platform |
| Version Model Number | 1.x.x |
| Company DUNS | 371379519 |
| Company Name | Neuroventis |
| 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 | true |
| Serial Number | false |
| Manufacturing Date | true |
| 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 |