FINESSE ModifEYE 337.68

GUDID 17612717072074

27+ ModifEYE Soft Tip Backflush

Alcon Laboratories, Inc.

Vitrectomy fluid/gas handling handpiece/cannula

• Primary Device ID: 17612717072074
• NIH Device Record Key: f6064c53-eab9-4bf0-bec5-a4bc75479ee7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FINESSE ModifEYE
• Version Model Number: 337.68
• Catalog Number: 337.68
• Company DUNS: 008018525
• Company Name: Alcon Laboratories, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Dimensions

• Needle Gauge: 27 Gauge
• Needle Gauge: 27 Gauge
• Needle Gauge: 27 Gauge
• Needle Gauge: 27 Gauge
• Needle Gauge: 27 Gauge
• Needle Gauge: 27 Gauge
• Needle Gauge: 27 Gauge
• Needle Gauge: 27 Gauge
• Needle Gauge: 27 Gauge
• Needle Gauge: 27 Gauge
• Needle Gauge: 27 Gauge
• Needle Gauge: 27 Gauge

Device Identifiers

Device Issuing Agency	Device ID
GS1	07612717072077 [Primary]
GS1	17612717072074 [Package]; Contains: 07612717072077; Package: Box [6 Units]; In Commercial Distribution

FDA Product Code

• HMX: Cannula, Ophthalmic

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: 2024-10-03
• Device Publish Date: 2024-09-25

On-Brand Devices [FINESSE ModifEYE]

• 17612717072074: 27+ ModifEYE Soft Tip Backflush
• 17612717072067: 25G ModifEYE Soft Tip Backflush
• 17612717072104: 27+ ModifEYE Soft Tip Backflush - Long
• 17612717072098: 25G ModifEYE Soft Tip Backflush - Long