| Primary Device ID | 10840277406238 |
| NIH Device Record Key | 03010d79-8303-463d-ab75-48aaa595da38 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Plain Gut |
| Version Model Number | 1016PG |
| 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 | 00840277406231 [Primary] |
| GS1 | 10840277406238 [Package] Contains: 00840277406231 Package: [12 Units] In Commercial Distribution |
| GAL | Suture, Absorbable, Natural |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-02-05 |
| Device Publish Date | 2025-01-28 |
| 10840277406382 | Suture |
| 10840277406375 | Suture |
| 10840277406368 | Suture |
| 10840277406351 | Suture |
| 10840277406344 | Suture |
| 10840277406337 | Suture |
| 10840277406320 | Suture |
| 10840277406313 | Suture |
| 10840277406306 | Suture |
| 10840277406290 | Suture |
| 10840277406283 | Suture |
| 10840277406276 | Suture |
| 10840277406269 | Suture |
| 10840277406252 | Suture |
| 10840277406245 | Suture |
| 10840277406238 | Suture |
| 10840277406221 | Suture |