| Primary Device ID | 10812444029502 |
| NIH Device Record Key | 7b6aa6d8-72d5-47ce-8649-a3b028458c79 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Vilet II Quick |
| Version Model Number | VGQ392C |
| 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 | 00812444029505 [Primary] |
| GS1 | 10812444029502 [Package] Contains: 00812444029505 Package: [12 Units] In Commercial Distribution |
| GAM | Suture, Absorbable, Synthetic, Polyglycolic Acid |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-07-07 |
| Device Publish Date | 2022-06-29 |
| 10812444025870 | Suture |
| 10812444025771 | SUTURE |
| 10812444024699 | SUTURE |
| 10812444024682 | SUTURE |
| 10812444024675 | SUTURE |
| 10812444024668 | SUTURE |
| 00812444024517 | SUTURE |
| 10812444024507 | Suture |
| 10812444024262 | SUTURE |
| 10812444024255 | SUTURE |
| 10812444024248 | SUTURE |
| 10812444024224 | SUTURE |
| 10812444024217 | SUTURE |
| 10812444024200 | SUTURE |
| 10812444024187 | SUTURE |
| 10812444024170 | SUTURE |
| 10812444023395 | SUTURE |
| 10810020083467 | suture |
| 00810020083453 | suture |
| 10812444023388 | Suture |
| 10810020088509 | Suture |
| 10812444029502 | Suture |
| 10812444029496 | Suture |
| 10810020086949 | Suture |
| 10810020080008 | Suture |