25ga Diffusion Light Pipe

GUDID 00817489027301

25ga Diffusion Light Pipe, 19ga Needle Connector

KATALYST SURGICAL LLC

Ophthalmic laser system beam guide

• Primary Device ID: 00817489027301
• NIH Device Record Key: 2a4f96ab-560b-442e-8956-c6a7b5678d7b
• Commercial Distribution Discontinuation: 2025-07-01
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: 25ga Diffusion Light Pipe
• Version Model Number: V2012-25R
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817489027301 [Unit of Use]
GS1	10817489027308 [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: 2
• Public Version Date: 2025-07-03
• Device Publish Date: 2020-11-06

On-Brand Devices [25ga Diffusion Light Pipe]

• 00840096211450: 25ga Diffusion Light Pipe, Short 19ga Needle Connector
• 00817489027301: 25ga Diffusion Light Pipe, 19ga Needle Connector