| Primary Device ID | 10884450685157 |
| NIH Device Record Key | c40e83ac-a086-4192-8b23-01f666dfd557 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ReSolve® |
| Version Model Number | 00884450685150 |
| Catalog Number | RBDC-8-038/D |
| 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 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
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| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00884450685150 [Primary] |
| GS1 | 10884450685157 [Package] Contains: 00884450685150 Package: [5 Units] In Commercial Distribution |
| FGE | Stents, drains and dilators for the biliary ducts |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-07-05 |
| Device Publish Date | 2023-06-27 |
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