| Primary Device ID | 10884450453091 |
| NIH Device Record Key | 7974479e-cd22-416f-babf-7ec076b868b8 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ReSolve ConvertX® |
| Version Model Number | 00884450453094 |
| Catalog Number | RCX22-10-038 |
| 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 | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |