Centurion

GUDID 00380657530571

Centurion Vision System With Active Sentry

Alcon Laboratories, Inc.

Phacoemulsification system Phacoemulsification system Phacoemulsification system Phacoemulsification system Phacoemulsification system Phacoemulsification system Phacoemulsification system Phacoemulsification system Phacoemulsification system Phacoemulsification system Phacoemulsification system Phacoemulsification system Phacoemulsification system Phacoemulsification system Phacoemulsification system Phacoemulsification system

• Primary Device ID: 00380657530571
• NIH Device Record Key: c44eec62-6867-4c74-a3d9-b21bae8c40b8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Centurion
• Version Model Number: 8065753057
• Company DUNS: 008018525
• Company Name: Alcon Laboratories, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00380657530571 [Primary]

FDA Product Code

• HQC: Unit, phacofragmentation

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-05-02
• Device Publish Date: 2023-04-24

On-Brand Devices [Centurion]

• 00380657517749: Centurion Remote Control
• 00380657517633: Centurion vision System
• 00380657517626: Centurion Vision System Footswitch
• 00380657530571: Centurion Vision System With Active Sentry