| Primary Device ID | 27290114060763 |
| NIH Device Record Key | fe687add-07be-449f-82dd-9e27692fcbe9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Neuro Omega with NeuroFortis drive + 2 basic stimulation Slots |
| Version Model Number | Neuro Omega with NeuroFortis drive + 2 basic stim |
| Catalog Number | NOW-NFF000-00 |
| Company DUNS | 531856466 |
| Company Name | ALPHA OMEGA ENGINEERING CO. LTD. |
| 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 | true |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| 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 |