AQUACLEAR

GUDID 00686715399532

COOPERVISION, INC.

Multi-purpose soft/rigid contact lens solution Multi-purpose soft/rigid contact lens solution

• Primary Device ID: 00686715399532
• NIH Device Record Key: cf0d9154-1a02-4bdb-8a4c-9b2164d7db4d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AQUACLEAR
• Version Model Number: NA
• Company DUNS: 829672323
• Company Name: COOPERVISION, INC.
• Device Count: 3
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00686715399532 [Primary]
GS1	00686715399549 [Unit of Use]

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: 2017-10-20

On-Brand Devices [AQUACLEAR]

• 00686715399556: NA
• 00686715399532: NA
• 00686715399518: NA
• 00686715399495: NA