60-0812-001

GUDID 10653405008484

7-1/2" HAND-SWITCHING MONOPOLAR ELECTROSURGICAL FORCEPS

Conmed Corporation

Endoscopic electrosurgical electrode, bipolar, reusable

• Primary Device ID: 10653405008484
• NIH Device Record Key: 911d7669-eb96-4255-afef-700248251522
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 60-0812-001
• Catalog Number: 60-0812-001
• 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: 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

Customer Support Contacts

• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	10653405008484 [Direct Marking]
GS1	20653405008481 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K964176

FDA Product Code

• GEI: ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[10653405008484]

Moist Heat or Steam Sterilization

[10653405008484]

Moist Heat or Steam Sterilization

[10653405008484]

Moist Heat or Steam Sterilization

[10653405008484]

Moist Heat or Steam Sterilization

[10653405008484]

Moist Heat or Steam Sterilization

[10653405008484]

Moist Heat or Steam Sterilization

[10653405008484]

Moist Heat or Steam Sterilization

[10653405008484]

Moist Heat or Steam Sterilization

[10653405008484]

Moist Heat or Steam Sterilization

[10653405008484]

Moist Heat or Steam Sterilization

[10653405008484]

Moist Heat or Steam Sterilization

[10653405008484]

Moist Heat or Steam Sterilization

[10653405008484]

Moist Heat or Steam Sterilization

[10653405008484]

Moist Heat or Steam Sterilization

[10653405008484]

Moist Heat or Steam Sterilization

[10653405008484]

Moist Heat or Steam Sterilization

[10653405008484]

Moist Heat or Steam Sterilization

[10653405008484]

Moist Heat or Steam Sterilization

[10653405008484]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-24

Devices Manufactured by Conmed Corporation

• 30653405990486 - EZSTART: 2025-05-21 EZSTART INTERFERENCE SCREW, 6MM X 15MM, TITANIUM
• 30653405990493 - EZSTART: 2025-05-21 EZSTART INTERFERENCE SCREW, 6MM X 20MM, TITANIUM
• 30653405990509 - EZSTART: 2025-05-21 EZSTART INTERFERENCE SCREW, 7MM X 15MM, TITANIUM
• 30653405990516 - EZSTART: 2025-05-21 EZSTART INTERFERENCE SCREW, 7MM X 20MM, TITANIUM
• 30653405990523 - EZSTART: 2025-05-21 EZSTART INTERFERENCE SCREW, 7MM X 30MM, TITANIUM
• 30653405990530 - EZSTART: 2025-05-21 EZSTART INTERFERENCE SCREW, 8MM X 15MM, TITANIUM
• 30653405990547 - EZSTART: 2025-05-21 EZSTART INTERFERENCE SCREW, 8MM X 20MM, TITANIUM
• 30653405990554 - EZSTART: 2025-05-21 EZSTART INTERFERENCE SCREW, 8MM X 25MM, TITANIUM