CooperVision Lite Multipurpose Solution

GUDID 00686715000049

COOPERVISION, INC.

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

• Primary Device ID: 00686715000049
• NIH Device Record Key: 1bb25b01-3400-4038-9521-f25f867812c0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CooperVision Lite Multipurpose Solution
• 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	00686715000049 [Primary]
GS1	00686715399464 [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: 2016-09-23

On-Brand Devices [CooperVision Lite Multipurpose Solution]

• 00686715000056: NA
• 00686715000049: NA