| Primary Device ID | 07290019352037 |
| NIH Device Record Key | a3a67072-f4bd-4ac8-9b45-8af8f64d5dc3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Lvivo Standalone UI |
| Version Model Number | Lvivo_UI |
| Company DUNS | 533365149 |
| Company Name | DIA IMAGING ANALYSIS LTD |
| 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 | false |
| Manufacturing Date | false |
| 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 |