136011

GUDID 30653405002912

FORCEPS,BIPLR,JWLRS,CURV,4",S

Conmed Corporation

Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable Endoscopic electrosurgical electrode, bipolar, reusable
Primary Device ID30653405002912
NIH Device Record Keye239222b-75b7-463f-a8c8-6a495229b397
Commercial Distribution Discontinuation2022-04-19
Commercial Distribution StatusNot in Commercial Distribution
Version Model Number136011
Catalog Number136011
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

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Device Identifiers

Device Issuing AgencyDevice ID
GS110653405002918 [Primary]
GS130653405002912 [Direct Marking]

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 Number4
Public Version Date2022-04-20
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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