| Primary Device ID | 10840277407549 |
| NIH Device Record Key | 60eb3b29-5431-40eb-bc0c-1047ae44a8ca |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PolyPro |
| Version Model Number | 1031P |
| 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 | 00840277407542 [Primary] |
| GS1 | 10840277407549 [Package] Contains: 00840277407542 Package: [12 Units] In Commercial Distribution |
| GAW | Suture, Nonabsorbable, Synthetic, Polypropylene |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-01-22 |
| Device Publish Date | 2025-01-14 |
| 10840277406160 | Suture |
| 10840277407785 | Suture |
| 10840277407778 | Suture |
| 10840277407761 | Suture |
| 10840277407754 | Suture |
| 10840277407747 | Suture |
| 10840277407730 | Suture |
| 10840277407600 | Suture |
| 10840277407594 | Suture |
| 10840277407587 | Suture |
| 10840277407570 | Suture |
| 10840277407563 | Suture |
| 10840277407556 | Suture |
| 10840277407549 | Suture |
| 10840277407532 | Suture |
| 10840277408805 | Suture |
| 10840277408461 | Suture |
| 10840277409123 | Suture |
| 10840277409116 | Suture |
| 10840277409109 | Suture |
| 10840277409093 | Suture |
| 10840277409079 | Suture |
| 10840277408508 | Suture |
| 10840277408492 | Suture |
| 00840277408471 | Suture |