| Primary Device ID | 10815098020222 |
| NIH Device Record Key | 87f0b3e4-f570-46cd-9e6a-b91e35df0a54 |
| Commercial Distribution Discontinuation | 2024-08-09 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | ReviveR View Configuration |
| Version Model Number | DDU-C2300 |
| Company DUNS | 128340200 |
| Company Name | DEFIBTECH, L.L.C. |
| 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 | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |