Centurion

GUDID 00380650005656

Centurion Vision System With Active Sentry without IV Pole

Alcon Laboratories, Inc.

Phacoemulsification system

• Primary Device ID: 00380650005656
• NIH Device Record Key: 502c119a-669d-480f-922f-71a3fb66f866
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Centurion
• Version Model Number: 8065000565
• 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	00380650005656 [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: 2024-08-02
• Device Publish Date: 2024-07-25

On-Brand Devices [Centurion]

• 00380657517749: Centurion Remote Control
• 00380657517633: Centurion vision System
• 00380657517626: Centurion Vision System Footswitch
• 00380657530571: Centurion Vision System With Active Sentry
• 00380650005656: Centurion Vision System With Active Sentry without IV Pole