LIQUID OPTICS INTERFACE LOI-12

GUDID 05050474604810

SINGLE LIQUID OPTICS INTERFACE,12

OPTIMEDICA CORPORATION

Ophthalmic laser system beam guide

• Primary Device ID: 05050474604810
• NIH Device Record Key: 9440030e-5fa1-414f-8e6b-2924b7d81721
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LIQUID OPTICS INTERFACE
• Version Model Number: LOI-12
• Catalog Number: LOI-12
• Company DUNS: 151018996
• Company Name: OPTIMEDICA CORPORATION
• 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(877)266-4543
• Email: JJV-US-SURGICALORDERS@ITS.JNJ.

Device Identifiers

Device Issuing Agency	Device ID
GS1	05050474604810 [Primary]

FDA Product Code

• OOE: Ophthalmic femtosecond laser

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-09-24
• Device Publish Date: 2016-09-02

On-Brand Devices [LIQUID OPTICS INTERFACE]

• 05050474604834: LIQUID OPTICS INTRFCE,12,BK PK,20 UNITS
• 05050474604827: LIQUID OPTICS INTRFC,STERILE, BULK PK,20
• 05050474604810: SINGLE LIQUID OPTICS INTERFACE,12
• 05050474604803: LIQUID OPTICS(TM) INTRFACE, STERILE, SGL