095450

GUDID 01816901021933

LEONI FIBER OPTICS, INC.

Urogenital surgical laser system beam guide, single-use

• Primary Device ID: 01816901021933
• NIH Device Record Key: 08c44bc9-14bd-47e0-893e-226984772a53
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: LFS-550-SB
• Catalog Number: 095450
• Company DUNS: 039281260
• Company Name: LEONI FIBER OPTICS, INC.
• Device Count: 1
• 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	00816901021934 [Primary]
GS1	01816901021933 [Package]; Contains: 00816901021934; Package: [5 Units]; In Commercial Distribution
GS1	02816901021932 [Package]; Package: [2 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K050738

FDA Product Code

• GEX: Powered laser surgical instrument

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: 2019-08-30
• Device Publish Date: 2019-08-22

Devices Manufactured by LEONI FIBER OPTICS, INC.

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