Infiniti

GUDID 00380657504039

Enhanced Footswitch, Infiniti

Alcon Laboratories, Inc.

Foot-switch, electrical

• Primary Device ID: 00380657504039
• NIH Device Record Key: 030ac0f7-c021-4b06-b0b0-47f224c13434
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Infiniti
• Version Model Number: 8065750403
• Company DUNS: 008018525
• Company Name: Alcon Laboratories, Inc.
• 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: false
• Serial Number: true
• 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)862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)862-5266
• Email: web.masterus@alcon.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00380657504039 [Primary]

FDA Product Code

• HQE: Instrument, vitreous aspiration and cutting, ac-powered

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-24

On-Brand Devices [Infiniti]

• 00380657521609: Infiniti Vision System
• 00380657504688: Infiniti Remote control
• 00380657504039: Enhanced Footswitch, Infiniti
• 10380657502933: Infiniti Ultrasound Multipak Basic Stand Alone
• 10380657501578: Anterior Vitrectomy Pak: Anterior Vitrectomy Probe w/21 GA Infusion Cannula
• 00380657501212: Ultrasonic Handpiece