Infiniti

GUDID 10380657502933

Infiniti Ultrasound Multipak Basic Stand Alone

Alcon Laboratories, Inc.

Foot-switch, electrical

• Primary Device ID: 10380657502933
• NIH Device Record Key: 738aa039-8813-4e0a-b2b5-c07562832f98
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Infiniti
• Version Model Number: 8065750293
• 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: 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)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	00380657502936 [Primary]
GS1	10380657502933 [Package]; Contains: 00380657502936; Package: Box [6 Units]; In Commercial Distribution

FDA Product Code

• HQC: Unit, phacofragmentation

Sterilization

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

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