| Primary Device ID | 00884838102965 |
| NIH Device Record Key | 8b217f94-a3cb-4b49-915a-a86eb8dec310 |
| Commercial Distribution Discontinuation | 2030-11-09 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Pinnacle Radiation Therapy Planning System |
| Version Model Number | 16.4 |
| Catalog Number | 45980163082X |
| Company DUNS | 829526560 |
| Company Name | Philips Medical Systems (cleveland), Inc. |
| Device Count | 1 |
| DM Exempt | true |
| 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 | true |
| Serial Number | false |
| 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 |