130146

GUDID 30653405002141

ELECTROSURGICAL FOOTSWITCH

Conmed Corporation

Argon-enhanced electrosurgical system Argon-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system Inert gas-enhanced electrosurgical system
Primary Device ID30653405002141
NIH Device Record Keyfefc9498-df7f-43dc-bcf9-4387338546b9
Commercial Distribution StatusIn Commercial Distribution
Version Model Number130146
Catalog Number130146
Company DUNS071595540
Company NameConmed Corporation
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM
Phone+1(800)237-0169
EmailCUSTOMER_SERVICE@CONMED.COM

Device Identifiers

Device Issuing AgencyDevice ID
GS110653405002147 [Direct Marking]
GS130653405002141 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEIELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-24

Devices Manufactured by Conmed Corporation

30845854026797 - GENESYS CrossFT, Hi-Fi2024-04-25 5.5 mm GENESYS CrossFT Suture Anchor with Three #2 (5 metric) Hi-Fi Sutures
30845854026803 - GENESYS CrossFT, Hi-Fi2024-04-25 6.5 mm GENESYS CrossFT Suture Anchor with Two #2 (5 metric) Hi-Fi Sutures
30845854026810 - GENESYS CrossFT, Hi-Fi2024-04-25 6.5 mm GENESYS CrossFT Suture Anchor with Three #2 (5 metric) Hi-Fi Sutures
30845854027862 - GENESYS PressFT, Hi-Fi2024-04-25 GENESYS PressFT 2.1 w/One #2 (5 metric) Hi-Fi Suture, HIP (1 White/Black)
30845854027893 - GENESYS PressFT, Hi-Fi2024-04-25 GENESYS PressFT 2.6 w/One #2 (5 metric) Hi-Fi Suture, HIP (1 White/Black)
30845854034600 - GENESYS CrossFT, Hi-Fi2024-04-25 GENESYS CrossFT 5.5 mm Suture Anchor, w/3 Hi-Fi #2 (5 metric) Sutures w/Needles
30845854034617 - GENESYS CrossFT, Hi-Fi2024-04-25 GENESYS CrossFT 6.5 mm Suture Anchor, w/2 Hi-Fi #2 (5 metric) Sutures w/Needles
30653405988643 - Argo Knotless GENESYS2024-04-22 5.5mm Argo Knotless® GENESYSTM Anchor

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