EndoMaster 098963

GUDID 01816901023050

LEONI FIBER OPTICS, INC.

Urogenital surgical laser system beam guide, single-use

• Primary Device ID: 01816901023050
• NIH Device Record Key: 13d143d5-71ad-4b75-a96d-435edd65ac7d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EndoMaster
• Version Model Number: LFS-272-SB
• Catalog Number: 098963
• Company DUNS: 039281260
• Company Name: LEONI FIBER OPTICS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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	00816901023051 [Primary]
GS1	01816901023050 [Package]; Contains: 00816901023051; Package: [5 Units]; In Commercial Distribution
GS1	02816901023059 [Package]; Package: [2 Units]; In Commercial Distribution

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: 2021-07-26
• Device Publish Date: 2021-07-16

On-Brand Devices [EndoMaster]

• 01816901023098: LFS-550-SB
• 01816901023074: LFS-365-SB
• 01816901023050: LFS-272-SB