| Primary Device ID | 30653405988766 |
| NIH Device Record Key | 8a718f61-f051-4a06-ad29-0f0c3384f2f1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Argo Knotless GENESYS |
| Version Model Number | KBC4755DBP |
| Catalog Number | KBC4755DBP |
| Company DUNS | 071595540 |
| Company Name | Conmed Corporation |
| Device Count | 1 |
| DM Exempt | false |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| 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(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com | |
| Phone | +1(866)426-6633 |
| CustomerExperience@conmed.com |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY;DO NOT CRUSH;DO NOT REUSE;DO NOT RESTERILIZE |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY;DO NOT CRUSH;DO NOT REUSE;DO NOT RESTERILIZE |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY;DO NOT CRUSH;DO NOT REUSE;DO NOT RESTERILIZE |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY;DO NOT CRUSH;DO NOT REUSE;DO NOT RESTERILIZE |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY;DO NOT CRUSH;DO NOT REUSE;DO NOT RESTERILIZE |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY;DO NOT CRUSH;DO NOT REUSE;DO NOT RESTERILIZE |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY;DO NOT CRUSH;DO NOT REUSE;DO NOT RESTERILIZE |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY;DO NOT CRUSH;DO NOT REUSE;DO NOT RESTERILIZE |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY;DO NOT CRUSH;DO NOT REUSE;DO NOT RESTERILIZE |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY;DO NOT CRUSH;DO NOT REUSE;DO NOT RESTERILIZE |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY;DO NOT CRUSH;DO NOT REUSE;DO NOT RESTERILIZE |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY;DO NOT CRUSH;DO NOT REUSE;DO NOT RESTERILIZE |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY;DO NOT CRUSH;DO NOT REUSE;DO NOT RESTERILIZE |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY;DO NOT CRUSH;DO NOT REUSE;DO NOT RESTERILIZE |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY;DO NOT CRUSH;DO NOT REUSE;DO NOT RESTERILIZE |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY;DO NOT CRUSH;DO NOT REUSE;DO NOT RESTERILIZE |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY;DO NOT CRUSH;DO NOT REUSE;DO NOT RESTERILIZE |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY;DO NOT CRUSH;DO NOT REUSE;DO NOT RESTERILIZE |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 20653405988769 [Primary] |
| GS1 | 30653405988766 [Package] Contains: 20653405988769 Package: CARTON [1 Units] In Commercial Distribution |
| LXH | Orthopedic manual surgical instrument |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-04-22 |
| Device Publish Date | 2024-04-12 |
| 10653405988601 | 4.75 mm Argo KnotlessTM GENESYSTM Reusable Smooth Punch |
| 10653405988595 | 5.5 mm Argo KnotlessTM GENESYSTM Reusable Tap |
| 10653405988588 | 4.75 mm Argo KnotlessTM GENESYSTM Reusable Tap |
| 10653405988571 | 4.75/5.5 mm Argo KnotlessTM GENESYSTM Reusable Broaching Punch |
| 30653405988766 | 4.75/5.5 mm Argo KnotlessTM GENESYSTM Disposable Broaching Punch |
| 30653405988759 | 4.75 mm Argo KnotlessTM GENESYSTM Disposable Smooth Punch |
| 30653405988742 | 4.75 mm Argo KnotlessTM GENESYSTM Disposable Tap |
| 30653405988735 | 5.5 mm Argo KnotlessTM GENESYSTM Disposable Tap |
| 30653405988698 | 4.75mm Argo Knotless® GENESYSTM Anchor, HI-FI Tape, White/Black |
| 30653405988681 | 4.75mm Argo Knotless® GENESYSTM Anchor, HI-FI Tape, Blue/Blue |
| 30653405988674 | 4.75mm Argo Knotless® GENESYSTM Anchor |
| 30653405988667 | 5.5mm Argo Knotless® GENESYSTM Anchor, HI-FI Tape, White/Black |
| 30653405988650 | 5.5mm Argo Knotless® GENESYSTM Anchor, HI-FI Tape, Blue/Blue |
| 30653405988643 | 5.5mm Argo Knotless® GENESYSTM Anchor |