ILLUMINATED LASER PROBE OS4, 23G, FLEXIBLE CURVED, STERILE/SINGLE USE

GUDID 10817489025359

ILLUMINATED LASER PROBE OS4, 23G, FLEXIBLE CURVED, STERILE/SINGLE USE

KATALYST SURGICAL LLC

Ophthalmic fibreoptic light instrument, single-use

• Primary Device ID: 10817489025359
• NIH Device Record Key: 7b06b07d-6f39-47e1-a6a2-85149fd60ca5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ILLUMINATED LASER PROBE OS4, 23G, FLEXIBLE CURVED, STERILE/SINGLE USE
• Version Model Number: VK400213
• 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	00081748902535 [Unit of Use]
GS1	10817489025359 [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: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-05-07
• Device Publish Date: 2017-08-17

Devices Manufactured by KATALYST SURGICAL LLC

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