| Primary Device ID | 00859032007200 |
| NIH Device Record Key | 025623c1-1be7-4fe5-aae3-a6db9c1d7897 |
| Commercial Distribution Discontinuation | 2024-12-19 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Panther TPS |
| Version Model Number | 5.8 |
| Company DUNS | 002162728 |
| Company Name | Prowess, Inc. |
| 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 | 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00859032007200 [Primary] |
| MUJ | System, Planning, Radiation Therapy Treatment |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-12-27 |
| Device Publish Date | 2024-12-19 |
| 00868603000236 | The purpose of Prowess Panther TPS is to provide a complete program for radiation therapy treatm |
| 00859032007132 | 5.7 |
| 00859032007088 | v5.61 |
| 00859032007064 | v5.6 |
| 00859032007279 | Panther TPS 6.0 |
| 00859032007255 | Panther TPS 5.9 |
| 00859032007231 | Panther TPS 5.81 |
| 00859032007200 | Panther TPS 5.8 |
| 00859032007194 | Panther TPS 5.7 DCP2 |
| 00859032007170 | Panther TPS 5.7 DCP |