| Primary Device ID | 10840277409406 |
| NIH Device Record Key | 65468f24-c488-4cf9-9a51-9526dec59690 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Riverlon |
| Version Model Number | 1915BK |
| Company DUNS | 964053560 |
| Company Name | RIVERPOINT MEDICAL, LLC |
| 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 | 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 | 00840277409409 [Primary] |
| GS1 | 10840277409406 [Package] Contains: 00840277409409 Package: [12 Units] In Commercial Distribution |
| GAR | Suture, Nonabsorbable, Synthetic, Polyamide |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-06-26 |
| Device Publish Date | 2025-06-18 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() RIVERLON 73269349 1199615 Dead/Cancelled |
Dan River Inc. 1980-07-07 |