| Primary Device ID | 00896208000818 |
| NIH Device Record Key | 321e89f5-1b57-43be-b67c-5b2192affbbd |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PERCEVAL PLUS |
| Version Model Number | PVF-L |
| Company DUNS | 243661431 |
| Company Name | Livanova Canada Corp |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | false |
| Serial Number | true |
| 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 |