| Primary Device ID | 20845854042530 |
| NIH Device Record Key | 7c07c8e0-765a-44fd-8c9f-e0e7b9d0f437 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SUPER REVO |
| Version Model Number | CF6140HNB |
| Catalog Number | CF6140HNB |
| Company DUNS | 071595540 |
| Company Name | Conmed Corporation |
| 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 | 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 |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| Outer Diameter | 5 Millimeter |
| 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 |
| 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 |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10845854042533 [Package] Package: Carton [1 Units] In Commercial Distribution |
| GS1 | 20845854042530 [Primary] |
| MBI | FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-03-21 |
| Device Publish Date | 2015-10-24 |
| 20845854042530 | SUPER REVO-FT 5.0MM SUTURE ANCHOR W/ 2 HI-FI NO. 2 (5 METRIC) SUTURES W/ NEEDLES |
| 20845854042516 | 5.0MM SUPER REVO-FT SUTURE ANCHOR WITH TWO NO. 2 (5 METRIC) HI-FI SUTURES |
| 20845854019822 | 5MM SUPER REVO ANCHOR, PRETHREADED, NO. 2 HIFI |
| 20845854019815 | 5MM SUPER REVO IMPLANT ONLY, TWO USP NO. 2 BRAIDED SUTURES |
| 20845854018948 | SUPER REVO-FT 5.0MM SUTURE ANCHOR W/ 2 HI-FI NO. 2 (5 METRIC) SUTURES W/ NEEDLES |
| 20845854015848 | 5MM SUPER REVO WITH DISPOSABLE DRIVER, TWO NO. 2 HI-FI SUTURES |
| 20845854014254 | 5.0MM THREVO-FT SUTURE ANCHOR WITH THREE NO. 2 (5 METRIC) HI-FI SUTURES |
| 20845854013462 | 5.0MM SUPER REVO-FT SUTURE ANCHOR WITH TWO NO. 2 (5 METRIC) HI-FI SUTURES |
| 20845854012311 | 5MM SUPER REVO WITH DISPOSABLE DRIVER, TWO USP NO. 2 BRAIDED SUTURES |
| 10845854030844 | SUPER REVO REUSABLE DRIVER |