| Primary Device ID | 10803622105422 |
| NIH Device Record Key | aaf48dc9-43b7-4b4f-aed0-0f4da37efdac |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Venous cardiopulmonary bypass cannula |
| Version Model Number | RD-xxxxx |
| Company DUNS | 080914995 |
| Company Name | LIVANOVA USA, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| 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 |