| Primary Device ID | 10840277409048 |
| NIH Device Record Key | 91ec7b54-0bf6-4eb7-8ee6-f5c5d6799e38 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Mono-dox |
| Version Model Number | M467 |
| 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 | 00840277409041 [Primary] |
| GS1 | 10840277409048 [Package] Contains: 00840277409041 Package: [12 Units] In Commercial Distribution |
| NEW | Suture, Surgical, Absorbable, Polydioxanone |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-03-21 |
| Device Publish Date | 2025-03-13 |
| 10840277407334 | Suture |
| 10840277407327 | Suture |
| 00840277407313 | Suture |
| 10840277409062 | Suture |
| 10840277409055 | Suture |
| 10840277409048 | Suture |
| 10840277409031 | Suture |
| 10840277409024 | Suture |
| 10840277409017 | Suture |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MONO-DOX 76406679 2715469 Live/Registered |
CP MEDICAL 2002-05-10 |