OPTI-FREE

GUDID 00300650180078

OPTI-FREE Contact Lens Cases

Alcon Laboratories, Inc.

Contact lens case

• Primary Device ID: 00300650180078
• NIH Device Record Key: 7cddd9d3-48f1-4130-9393-1ddf4b03d71a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OPTI-FREE
• Version Model Number: OPTI-FREE LENS CASE
• Company DUNS: 008018525
• Company Name: Alcon Laboratories, Inc.
• Device Count: 2
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: +1(800)241-5999
• Email: web.masterus@alcon.com
• Phone: +1(800)241-5999
• Email: web.masterus@alcon.com
• Phone: +1(800)241-5999
• Email: web.masterus@alcon.com
• Phone: +1(800)241-5999
• Email: web.masterus@alcon.com
• Phone: +1(800)241-5999
• Email: web.masterus@alcon.com
• Phone: +1(800)241-5999
• Email: web.masterus@alcon.com
• Phone: +1(800)241-5999
• Email: web.masterus@alcon.com
• Phone: +1(800)241-5999
• Email: web.masterus@alcon.com
• Phone: +1(800)241-5999
• Email: web.masterus@alcon.com
• Phone: +1(800)241-5999
• Email: web.masterus@alcon.com
• Phone: +1(800)241-5999
• Email: web.masterus@alcon.com
• Phone: +1(800)241-5999
• Email: web.masterus@alcon.com
• Phone: +1(800)241-5999
• Email: web.masterus@alcon.com
• Phone: +1(800)241-5999
• Email: web.masterus@alcon.com
• Phone: +1(800)241-5999
• Email: web.masterus@alcon.com
• Phone: +1(800)241-5999
• Email: web.masterus@alcon.com
• Phone: +1(800)241-5999
• Email: web.masterus@alcon.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00300650180009 [Unit of Use]
GS1	00300650180078 [Primary]
GS1	20300650180072 [Package]; Package: Case [24 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K971618

FDA Product Code

• LRX: Case, contact lens

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-24

On-Brand Devices [OPTI-FREE]

• 00300650180078: OPTI-FREE Contact Lens Cases
• 00300650180023: OPTI-FREE LENS CASE
• 00300650106207: OPTI-FREE Daily Cleaner 20ml