Primary Device ID | 10845854030844 |
NIH Device Record Key | de9c5f6b-f344-4073-8ede-9259d02ec455 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SUPER REVO |
Version Model Number | C6142 |
Catalog Number | C6142 |
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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10845854030844 [Primary] |
GS1 | 20845854030841 [Direct Marking] |
LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-10-14 |
Device Publish Date | 2021-10-06 |
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 |