| Primary Device ID | 04056481004095 |
| NIH Device Record Key | 0af6e2c1-eb00-47cc-96f5-3a85ca548faa |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Phantom Pointer |
| Version Model Number | 40900-1 |
| Catalog Number | 40900-1 |
| Company DUNS | 314482980 |
| Company Name | Brainlab AG |
| 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 | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| 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 |