| Primary Device ID | 00868201000157 |
| NIH Device Record Key | d3507343-4087-45ea-8784-77e9cf8743c9 |
| Commercial Distribution Discontinuation | 2021-07-29 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Wizard CaP |
| Version Model Number | 10 cc |
| Company DUNS | 078400984 |
| Company Name | Vivorte, 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |