Clareon Vivity Extended Vision Hydrophobic IOL with the AutonoMe CNAET0.095

GUDID 00380652406093

CLAREON VIVITY AUTONOME

Alcon Laboratories, Inc.

Posterior-chamber intraocular lens, pseudophakic

• Primary Device ID: 00380652406093
• NIH Device Record Key: 1e6e8aa3-5542-4e68-8a1c-22457ec53ed2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Clareon Vivity Extended Vision Hydrophobic IOL with the AutonoMe
• Version Model Number: CNAET0
• Catalog Number: CNAET0.095
• 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: true
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00380652406093 [Primary]

FDA Product Code

• POE: Extended Depth Of Focus Intraocular Lens

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: 2025-03-12
• Device Publish Date: 2025-03-04

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