| Primary Device ID | 10884450721244 |
| NIH Device Record Key | a8b9c392-e0bc-44e5-b2cc-4803faf47177 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ReSolve ConvertX® |
| Version Model Number | C |
| Catalog Number | RCX20-10-038 |
| Company DUNS | 184763290 |
| Company Name | Merit Medical Systems, Inc. |
| 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 | 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 |