| Primary Device ID | 27290114063191 |
| NIH Device Record Key | dcb7db5d-027c-4b47-9b3d-2b7b093d6186 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Neuro Omega with Neuro Omega Drive Headstage + 2 basic stimulation Slots |
| Version Model Number | Neuro Omega with Neuro Omega Drive Headstage + 2 |
| Catalog Number | NOW-DFF000-00 |
| Company DUNS | 531856466 |
| Company Name | ALPHA OMEGA ENGINEERING CO. LTD. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| 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 |