136000

GUDID 30653405002882

Bipolar Forceps 6 Inch Omni Straight Electrosurgical Forceps

Conmed Corporation

Endoscopic electrosurgical electrode, bipolar, reusable

• Primary Device ID: 30653405002882
• NIH Device Record Key: fd439378-309d-4fee-a708-ef4846334cad
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 136000
• Catalog Number: 136000
• 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

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 Identifiers

Device Issuing Agency	Device ID
GS1	20653405002885 [Primary]
GS1	30653405002882 [Direct Marking]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K811820

FDA Product Code

• GEI: ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

Sterilization

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

[30653405002882]

Moist Heat or Steam Sterilization

[30653405002882]

Moist Heat or Steam Sterilization

[30653405002882]

Moist Heat or Steam Sterilization

[30653405002882]

Moist Heat or Steam Sterilization

[30653405002882]

Moist Heat or Steam Sterilization

[30653405002882]

Moist Heat or Steam Sterilization

[30653405002882]

Moist Heat or Steam Sterilization

[30653405002882]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-24

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