| Primary Device ID | 00860010859704 |
| NIH Device Record Key | 15fca53a-d89f-4b52-b1d2-efee3190c025 |
| Commercial Distribution Discontinuation | 2030-12-31 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | OneScope Pro |
| Version Model Number | OneScope Pro Video Laryngoscope |
| Company DUNS | 116913619 |
| Company Name | One-AI Healthcare, Inc |
| 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 | true |
| 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 |