OPTI-FREE EXPRESS

GUDID 00300650193207

OPTI-FREE EXPRESS Rewetting Drops 20ml

Alcon Laboratories, Inc.

Contact lens wetting solution

• Primary Device ID: 00300650193207
• NIH Device Record Key: 4ad628de-9200-4883-affc-361b921de0a0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OPTI-FREE EXPRESS
• Version Model Number: OPTI-FREE EXPRESS 20ml
• 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: false
• OTC Over-The-Counter: true

Customer Support Contacts

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00300650193207 [Primary]
GS1	20300650193119 [Package]; Package: Case [24 Units]; In Commercial Distribution

FDA Product Code

• LPN: Accessories, soft lens products

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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