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

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