| Primary Device ID | 05056190500740 |
| NIH Device Record Key | 312300fe-c645-48f3-bbd8-f38488fd6254 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DoseRT camera |
| Version Model Number | DoseRT camera |
| Catalog Number | DoseRT camera |
| Company DUNS | 222160801 |
| Company Name | VISION RT LIMITED |
| 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 | 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05056190500740 [Primary] |
| IYE | Accelerator, Linear, Medical |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-04-11 |
| Device Publish Date | 2024-04-03 |
| 05056190500962 - AlignRT Plus | 2024-07-31 |
| 05056190500979 - AlignRT Plus | 2024-07-31 |
| 05056190500986 - AlignRT Plus | 2024-07-31 |
| 05056190500733 - Respiratory Module | 2024-06-24 Respiratory Module software module. |
| 05056190500726 - AlignRT 7.3 (software) | 2024-04-11 AlignRT 7.3 (software) used on AlignRT Plus systems |
| 05056190500740 - DoseRT camera | 2024-04-11DoseRT camera used for AlignRT Plus systems. |
| 05056190500740 - DoseRT camera | 2024-04-11 DoseRT camera used for AlignRT Plus systems. |
| 05056190500825 - Patient ID Module | 2024-04-11 Patient ID Module used as accessory to AlignRT Plus |
| 05056190500894 - DoseRT reference board | 2024-04-11 DoseRT reference board used with AlignRT Plus systems. |