| Primary Device ID | 08809394330319 |
| NIH Device Record Key | 7f78ca65-f22d-4c90-97f9-063d15936144 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VIVIX-S 3643VAW |
| Version Model Number | FXRD-3643VAW |
| Company DUNS | 688274778 |
| Company Name | VIEWORKS CO., 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 | true |
| 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 | 08809394330319 [Primary] |
| MQB | Solid State X-Ray Imager (Flat Panel/Digital Imager) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-10-14 |
| Device Publish Date | 2020-10-06 |
| 08809394330357 - VIVIX-M 1824S | 2025-07-23 |
| 08809394330364 - VIVIX-M 2430S | 2025-07-23 |
| 08809394330678 - VIVIX-S 1751S | 2025-01-31 |
| 08809394330265 - VIVIX-S 1012N | 2024-08-09 |
| 08809394330272 - VIVIX-S 1012N | 2024-08-09 |
| 08809394330388 - QXLink | 2024-08-09 |
| 08809394330258 - VIVIX-S 1717V | 2024-08-01 Solid State X-ray Imager (flat panel/digital imager) |
| 08809394330586 - VIVIX-S FW | 2023-10-23 |