CENTURION® INTREPID®

GUDID 10380657531346

Active FMS w INTERPID Ultra Sleeves 0.9MM 30° ABS* INTERPID Hybrid Tip

Alcon Laboratories, Inc.

Ophthalmic surgical procedure kit, non-medicated, single-use

• Primary Device ID: 10380657531346
• NIH Device Record Key: dc44d9b1-da50-4caa-9583-e4fd1561e23f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CENTURION® INTREPID®
• Version Model Number: 8065753134
• 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: false
• Manufacturing Date: true
• Expiration Date: true
• 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	00380657531349 [Primary]
GS1	10380657531346 [Package]; Contains: 00380657531349; Package: [6 Units]; In Commercial Distribution

FDA Product Code

• HQC: Unit, phacofragmentation

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: 2022-01-24
• Device Publish Date: 2020-11-13

On-Brand Devices [CENTURION® INTREPID®]

• 10380657529015: SMALL PARTS KIT W/ INTREPID® NANO SLEEVES 0.9 MM Tipless
• 10380657531360: Active FMS w INTERPID Nano Sleeves 0.9MM 30° ABS* INTERPID Hybrid Tip
• 10380657531346: Active FMS w INTERPID Ultra Sleeves 0.9MM 30° ABS* INTERPID Hybrid Tip