| Primary Device ID | 00854393006039 |
| NIH Device Record Key | 0267a3f6-ae11-4caf-99fb-de84203fe40e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Velocity |
| Version Model Number | 4.2 |
| Company DUNS | 009120817 |
| Company Name | VARIAN MEDICAL SYSTEMS, 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 | 00854393006039 [Primary] |
| LLZ | System, image processing, radiological |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-05-22 |
| Device Publish Date | 2024-05-14 |
| 00854393006008 | 3.2 |
| 00854393006039 | 4.2 |