7-221-L

GUDID 40653405013533

5/8" NEEDLE ELECTRODE LONG SHAFT

Conmed Corporation

Open-surgery electrosurgical electrode, monopolar, reusable

• Primary Device ID: 40653405013533
• NIH Device Record Key: 85839c5c-dcaa-4436-bc23-a92ce5013aff
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 7-221-L
• Catalog Number: 7-221-L
• 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
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com
• Phone: +1(866)426-6633
• Email: CustomerExperience@conmed.com

Device Dimensions

• Outer Diameter: 0.625 Inch
• Outer Diameter: 0.625 Inch
• Outer Diameter: 0.625 Inch
• Outer Diameter: 0.625 Inch
• Outer Diameter: 0.625 Inch
• Outer Diameter: 0.625 Inch
• Outer Diameter: 0.625 Inch
• Outer Diameter: 0.625 Inch
• Outer Diameter: 0.625 Inch
• Outer Diameter: 0.625 Inch
• Outer Diameter: 0.625 Inch
• Outer Diameter: 0.625 Inch
• Outer Diameter: 0.625 Inch
• Outer Diameter: 0.625 Inch
• Outer Diameter: 0.625 Inch
• Outer Diameter: 0.625 Inch
• Outer Diameter: 0.625 Inch
• Outer Diameter: 0.625 Inch
• Outer Diameter: 0.625 Inch
• Outer Diameter: 0.625 Inch
• Outer Diameter: 0.625 Inch
• Outer Diameter: 0.625 Inch
• Outer Diameter: 0.625 Inch
• Outer Diameter: 0.625 Inch
• Outer Diameter: 0.625 Inch
• Outer Diameter: 0.625 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	30653405013536 [Primary]
GS1	40653405013533 [Direct Marking]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K800617

FDA Product Code

• GEI: ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

Sterilization

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

[40653405013533]

Moist Heat or Steam Sterilization

[40653405013533]

Moist Heat or Steam Sterilization

[40653405013533]

Moist Heat or Steam Sterilization

[40653405013533]

Moist Heat or Steam Sterilization

[40653405013533]

Moist Heat or Steam Sterilization

[40653405013533]

Moist Heat or Steam Sterilization

[40653405013533]

Moist Heat or Steam Sterilization

[40653405013533]

Moist Heat or Steam Sterilization

[40653405013533]

Moist Heat or Steam Sterilization

[40653405013533]

Moist Heat or Steam Sterilization

[40653405013533]

Moist Heat or Steam Sterilization

[40653405013533]

Moist Heat or Steam Sterilization

[40653405013533]

Moist Heat or Steam Sterilization

[40653405013533]

Moist Heat or Steam Sterilization

[40653405013533]

Moist Heat or Steam Sterilization

[40653405013533]

Moist Heat or Steam Sterilization

[40653405013533]

Moist Heat or Steam Sterilization

[40653405013533]

Moist Heat or Steam Sterilization

[40653405013533]

Moist Heat or Steam Sterilization

[40653405013533]

Moist Heat or Steam Sterilization

[40653405013533]

Moist Heat or Steam Sterilization

[40653405013533]

Moist Heat or Steam Sterilization

[40653405013533]

Moist Heat or Steam Sterilization

[40653405013533]

Moist Heat or Steam Sterilization

[40653405013533]

Moist Heat or Steam Sterilization

[40653405013533]

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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• 30653405990141 - PlumeSafe® X5™: 2024-10-22 PlumeSafe® X5™ Smoke Evacuation Unit with PlumeSafe® X5™ Smoke Evacuator Filter, 220V-240V 50/60 Hz
• 20653405990120 - BioBrace: 2024-09-30 BioBrace® Reinforced Implant, 23 x 25 mm
• 20653405990137 - BioBrace: 2024-09-30 BioBrace® Reinforced Implant, 35 x 25 mm