23ga Illuminated MultiFlex™ Inverted Extendable Laser Probe, Iridex Connector

GUDID 10817489027759

KATALYST SURGICAL LLC

Ophthalmic laser system beam guide

• Primary Device ID: 10817489027759
• NIH Device Record Key: b23ec691-cda9-4e5e-95f5-64d72a752390
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 23ga Illuminated MultiFlex™ Inverted Extendable Laser Probe, Iridex Connector
• Version Model Number: V6352E-23AR
• 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	00817489027752 [Unit of Use]
GS1	10817489027759 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K121187

FDA Product Code

• HQF: Laser, 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: 2019-04-11
• Device Publish Date: 2019-04-03

Devices Manufactured by KATALYST SURGICAL LLC

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