Alcon, Coherent

GUDID 10380650102031

2 GA Curved Laser Probe

Alcon Laboratories, Inc.

Ophthalmic laser system beam guide

• Primary Device ID: 10380650102031
• NIH Device Record Key: 31fe3f9a-4fbc-47aa-bf80-4916f54173d5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Alcon, Coherent
• Version Model Number: 8065010203
• 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

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00380650102034 [Primary]
GS1	10380650102031 [Package]; Contains: 00380650102034; Package: Box [6 Units]; In Commercial Distribution

FDA Product Code

• HQF: Laser, ophthalmic

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 [Alcon, Coherent]

• 10380657508034: 23 GA Straight Laser Probe
• 10380657501332: 25 GA Straight Laser Probe
• 10380650104196: 20 GA Straight Illuminated Laser Probe
• 10380650104035: 20 GA Curved Illuminated Laser Probe
• 10380650102192: 20 GA Straight Laser Probe
• 10380650102031: 2 GA Curved Laser Probe