Patient Interface 125 Kit

GUDID 04050555002086

Technolas Perfect Vision GmbH

Laser beam delivery unit holder Laser beam delivery unit holder Laser beam delivery unit holder Laser beam delivery unit holder Laser beam delivery unit holder Laser beam delivery unit holder Laser beam delivery unit holder Laser beam delivery unit holder Laser beam delivery unit holder Laser beam delivery unit holder Laser beam delivery unit holder Laser beam delivery unit holder 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