| Primary Device ID | 20845854053062 |
| NIH Device Record Key | d31fdb61-6fe9-4cd5-8842-0fb2a6417702 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | AV8570 |
| Catalog Number | AV8570 |
| Company DUNS | 071595540 |
| Company Name | Conmed Corporation |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 20845854053062 [Primary] |
| KQM | CAMERA, SURGICAL AND ACCESSORIES |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-07-31 |
| Device Publish Date | 2020-07-23 |
| 30653405988643 - Argo Knotless GENESYS | 2024-04-22 5.5mm Argo Knotless® GENESYSTM Anchor |
| 30653405988650 - Argo Knotless GENESYS | 2024-04-22 5.5mm Argo Knotless® GENESYSTM Anchor, HI-FI Tape, Blue/Blue |
| 30653405988667 - Argo Knotless GENESYS | 2024-04-22 5.5mm Argo Knotless® GENESYSTM Anchor, HI-FI Tape, White/Black |
| 30653405988674 - Argo Knotless GENESYS | 2024-04-22 4.75mm Argo Knotless® GENESYSTM Anchor |
| 30653405988681 - Argo Knotless GENESYS | 2024-04-22 4.75mm Argo Knotless® GENESYSTM Anchor, HI-FI Tape, Blue/Blue |
| 30653405988698 - Argo Knotless GENESYS | 2024-04-22 4.75mm Argo Knotless® GENESYSTM Anchor, HI-FI Tape, White/Black |
| 30653405988735 - Argo Knotless GENESYS | 2024-04-22 5.5 mm Argo KnotlessTM GENESYSTM Disposable Tap |
| 30653405988742 - Argo Knotless GENESYS | 2024-04-22 4.75 mm Argo KnotlessTM GENESYSTM Disposable Tap |