| Primary Device ID | 00854344007443 |
| NIH Device Record Key | 18d6e2d5-25de-4e5e-b2ba-e41608da2371 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Varex Digital Imaging System, Nexus, DRF, v3.2.0 |
| Version Model Number | Nexus DRF v3.2.0 |
| Company DUNS | 080506857 |
| Company Name | VAREX IMAGING CORPORATION |
| 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 | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |