Ascend

GUDID 00686715399655

COOPERVISION, INC.

Multi-purpose soft/rigid contact lens solution

• Primary Device ID: 00686715399655
• NIH Device Record Key: 688b3dd1-446a-49d0-8e42-ac15777108ba
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ascend
• Version Model Number: NA
• Company DUNS: 829672323
• Company Name: COOPERVISION, 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00686715399655 [Primary]

FDA Product Code

• LPN: Accessories, Soft Lens Products

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-05-20
• Device Publish Date: 2022-05-12

Devices Manufactured by COOPERVISION, INC.

• 00686715399655 - Ascend: 2022-05-20
• 00686715399655 - Ascend: 2022-05-20
• 00686715000049 - CooperVision Lite Multipurpose Solution: 2018-03-29
• 00686715000056 - CooperVision Lite Multipurpose Solution: 2018-03-29
• 00686715000339 - CooperVision Refine One Step: 2018-03-29
• 00686715000353 - CooperVision Refine One Step: 2018-03-29
• 00686715399495 - AQUACLEAR: 2018-03-29
• 00686715399518 - AQUACLEAR: 2018-03-29
• 00686715399532 - AQUACLEAR: 2018-03-29