Alcon, Infiniti, MicroSmooth, Kelman, ABS

GUDID 10380657410870

0.9 mm 30° Kelman® ABS® Tip

Alcon Laboratories, Inc.

Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use

• Primary Device ID: 10380657410870
• NIH Device Record Key: bdd498d1-445b-46ad-9db0-93d130f8851a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Alcon, Infiniti, MicroSmooth, Kelman, ABS
• Version Model Number: 8065741087
• 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

Device Dimensions

• Outer Diameter: 0.9 Millimeter
• Outer Diameter: 0.9 Millimeter
• Angle: 30 degree
• Outer Diameter: 0.9 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00380657410873 [Primary]
GS1	10380657410870 [Package]; Contains: 00380657410873; 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: 3
• Public Version Date: 2019-11-08
• Device Publish Date: 2016-09-24

On-Brand Devices [Alcon, Infiniti, MicroSmooth, Kelman, ABS]

• 10380657410887: 0.9 mm 45° Kelman® ABS® Tip
• 10380657410870: 0.9 mm 30° Kelman® ABS® Tip