| Primary Device ID | 00810123710584 |
| NIH Device Record Key | df4a6800-8592-4d44-8410-272d139bd7b4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Artix MT |
| Version Model Number | 32-102 / AS-01248 |
| Company DUNS | 076827459 |
| Company Name | INARI MEDICAL 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 | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | true |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |