LIGHTWAVE IA-2379-FC

GUDID 20845854040369

LIGHTWAVE ABLATOR 90 DEGREE ANGLE 3.2MM X 150MM

Conmed Corporation

Open-surgery electrosurgical electrode, monopolar, single-use

• Primary Device ID: 20845854040369
• NIH Device Record Key: d99c2e9e-e98a-41ae-ab1e-19349613bec2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LIGHTWAVE
• Version Model Number: IA-2379-FC
• Catalog Number: IA-2379-FC
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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

Device Dimensions

• Width: 3.2 Millimeter
• Length: 150 Millimeter
• Width: 3.2 Millimeter
• Length: 150 Millimeter
• Width: 3.2 Millimeter
• Length: 150 Millimeter
• Width: 3.2 Millimeter
• Length: 150 Millimeter
• Width: 3.2 Millimeter
• Length: 150 Millimeter
• Width: 3.2 Millimeter
• Length: 150 Millimeter
• Width: 3.2 Millimeter
• Length: 150 Millimeter
• Width: 3.2 Millimeter
• Length: 150 Millimeter
• Width: 3.2 Millimeter
• Length: 150 Millimeter
• Width: 3.2 Millimeter
• Length: 150 Millimeter
• Width: 3.2 Millimeter
• Length: 150 Millimeter
• Width: 3.2 Millimeter
• Length: 150 Millimeter
• Width: 3.2 Millimeter
• Length: 150 Millimeter
• Width: 3.2 Millimeter
• Length: 150 Millimeter
• Width: 3.2 Millimeter
• Length: 150 Millimeter
• Width: 3.2 Millimeter
• Length: 150 Millimeter
• Width: 3.2 Millimeter
• Length: 150 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	20845854040369 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K083281

FDA Product Code

• GEI: ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-02-07
• Device Publish Date: 2016-09-24

On-Brand Devices [LIGHTWAVE]

• 20845854040369: LIGHTWAVE ABLATOR 90 DEGREE ANGLE 3.2MM X 150MM
• 20845854040352: LIGHTWAVE ABLATOR, 90 DEGREE ANGLE, 3.2MM X 150MM
• 20845854040345: LIGHTWAVE SUCTION ABLATOR
• 10845854040348: LightWave Suction Ablator