| Primary Device ID | 20884450458543 |
| NIH Device Record Key | a44c48bb-c535-4d57-9c6c-f7bb9aedbd3a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ReSolve ConvertX® |
| Version Model Number | 00884450458549 |
| Catalog Number | RCX22-8-038/A |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00884450458549 [Primary] |
| GS1 | 10884450458546 [Package] Contains: 00884450458549 Package: [1 Units] In Commercial Distribution |
| GS1 | 20884450458543 [Package] Contains: 10884450458546 Package: [5 Units] In Commercial Distribution |
| FAD | Stent, ureteral |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-09-17 |
| Device Publish Date | 2020-09-09 |