Patient Interface 125 Kit

GUDID 04050555002086

Technolas Perfect Vision GmbH

Laser beam delivery unit holder

• Primary Device ID: 04050555002086
• NIH Device Record Key: 97276500-8533-4278-86d9-68cd046dfa52
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Patient Interface 125 Kit
• Version Model Number: 90000145
• Company DUNS: 341325716
• Company Name: Technolas Perfect Vision GmbH
• 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: false
• 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	04050555002086 [Primary]

FDA Product Code

• OOE: Ophthalmic Femtosecond Laser

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: 2024-03-21
• Device Publish Date: 2024-03-13

On-Brand Devices [Patient Interface 125 Kit]

• 04050555000990: Patient Interface Kit for VICTUS™ Femtosecond Laser Platform (software version 2.7 and higher)
• 04050555002086: 90000145