| Primary Device ID | 27290114062422 |
| NIH Device Record Key | f883157f-d005-4c3b-bad1-dea9852f6b7f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Neuro Omega with NeuroFortis Drive Headstage |
| Version Model Number | Neuro Omega with NeuroFortis Drive Headstage |
| Catalog Number | NOW-020070-00 |
| 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 |