CLERZ

GUDID 00300650192101

CLERZ Plus Lens Drops 8ml

Alcon Laboratories, Inc.

Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution Contact lens wetting solution

• Primary Device ID: 00300650192101
• NIH Device Record Key: 102b2c86-166a-455f-873e-d9c5e99dcab8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CLERZ
• Version Model Number: CLERZ 8ml
• 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
• 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
• 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	00300650192101 [Primary]
GS1	00300650192163 [Package]; Package: Case [24 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K984573

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: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-24

On-Brand Devices [CLERZ]

• 00300650192101: CLERZ Plus Lens Drops 8ml
• 00300650192057: CLERZ Plus Lens Drops 5ml