23ga Focal Light Pipe

GUDID 10817489025588

23ga Focal Light Pipe

KATALYST SURGICAL LLC

Ophthalmic laser system beam guide

• Primary Device ID: 10817489025588
• NIH Device Record Key: cdd00e50-2339-4229-8c7a-50e502b233eb
• Commercial Distribution Discontinuation: 2025-07-01
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: 23ga Focal Light Pipe
• Version Model Number: V2000-23R
• Company DUNS: 007883297
• Company Name: KATALYST SURGICAL LLC
• Device Count: 10
• 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	00817489025581 [Unit of Use]
GS1	10817489025588 [Primary]

FDA Product Code

• MPA: Endoilluminator

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2025-07-03
• Device Publish Date: 2017-10-13

On-Brand Devices [23ga Focal Light Pipe]

• 10817489025595: 23ga Focal Light Pipe
• 10817489025588: 23ga Focal Light Pipe