Alcon, Kelman, TurboSonics, ABS, MicroTip

GUDID 10380657900197

0° Round, 0.9 mm TurboSonics® ABS® MicroTip™ Tip

Alcon Laboratories, Inc.

Phacoemulsification system handpiece tip, single-use Phacoemulsification system handpiece tip, single-use Phacoemulsification system handpiece tip, single-use Phacoemulsification system handpiece tip, single-use Phacoemulsification system handpiece tip, single-use Phacoemulsification system handpiece tip, single-use Phacoemulsification system handpiece tip, single-use Phacoemulsification system handpiece tip, single-use Phacoemulsification system handpiece tip, single-use Phacoemulsification system handpiece tip, single-use Phacoemulsification system handpiece tip, single-use Phacoemulsification system handpiece tip, single-use Phacoemulsification system handpiece tip, single-use Phacoemulsification system handpiece tip, single-use Phacoemulsification system handpiece tip, single-use Phacoemulsification system handpiece tip, single-use Phacoemulsification system handpiece tip, single-use Phacoemulsification system handpiece tip, single-use

• Primary Device ID: 10380657900197
• NIH Device Record Key: 90bc0ff9-a495-485e-9c83-a32b0559e039
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Alcon, Kelman, TurboSonics, ABS, MicroTip
• Version Model Number: 8065790019
• 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: true
• 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
• Phone: +1(800)862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)862-5266
• Email: web.masterus@alcon.com
• Phone: +1(800)862-5266
• Email: web.masterus@alcon.com

Device Dimensions

• Angle: 0 degree
• Angle: 0 degree
• Outer Diameter: 0.9 Millimeter
• Angle: 0 degree
• Outer Diameter: 0.9 Millimeter
• Angle: 0 degree
• Outer Diameter: 0.9 Millimeter
• Angle: 0 degree
• Outer Diameter: 0.9 Millimeter
• Angle: 0 degree
• Outer Diameter: 0.9 Millimeter
• Angle: 0 degree
• Outer Diameter: 0.9 Millimeter
• Angle: 0 degree
• Outer Diameter: 0.9 Millimeter
• Angle: 0 degree
• Outer Diameter: 0.9 Millimeter
• Angle: 0 degree
• Outer Diameter: 0.9 Millimeter
• Angle: 0 degree
• Outer Diameter: 0.9 Millimeter
• Angle: 0 degree
• Outer Diameter: 0.9 Millimeter
• Angle: 0 degree
• Outer Diameter: 0.9 Millimeter
• Angle: 0 degree
• Outer Diameter: 0.9 Millimeter
• Angle: 0 degree
• Outer Diameter: 0.9 Millimeter
• Angle: 0 degree
• Outer Diameter: 0.9 Millimeter
• Angle: 0 degree
• Outer Diameter: 0.9 Millimeter
• Angle: 0 degree
• Outer Diameter: 0.9 Millimeter
• Angle: 0 degree

Device Identifiers

Device Issuing Agency	Device ID
GS1	00380657900190 [Primary]
GS1	10380657900197 [Package]; Contains: 00380657900190; 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

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• 10380650000535 - LENSX: 2022-11-14 LENSX LASER SOFTFIT PATIENT INTERFACE 10 PK, EO
• 20380650000549 - LENSX: 2022-11-14 LENSX SOFTFIT PATIENT INTERFACE NOMINAL,EO
• 20380650000556 - LENSX: 2022-11-14 LENSX SOFTFIT PATIENT INTERFACE STEEP,EO