Opti-Tip

GUDID 07290117771747

17290117771751 - Opti-Tip Pack 17290117771799 - Opti-Tip Master Pack

LUMENIS BE LTD

Intense pulsed light dry eye therapy unit

• Primary Device ID: 07290117771747
• NIH Device Record Key: 0d9a5b93-5863-4676-9a29-9c164510c9b7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Opti-Tip
• Version Model Number: NA
• Company DUNS: 600763501
• Company Name: LUMENIS BE LTD
• 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• 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	07290117771747 [Primary]
GS1	17290117771751 [Package]; Package: [24 Units]; In Commercial Distribution
GS1	17290117771799 [Package]; Package: [48 Units]; In Commercial Distribution

FDA Product Code

• QIU: Intense Pulsed Light Device For Managing Dry Eye

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-03-29
• Device Publish Date: 2023-03-21

Devices Manufactured by LUMENIS BE LTD

• 07290117772447 - FoLiCool™ Tip: 2024-03-25
• 07290117772522 - FoLix™: 2024-03-25
• 07290117772539 - FoLix™ Handpiece: 2024-03-25
• 07290117772393 - LUSTER System: 2024-01-30
• 07290117772409 - LUSTER Handpiece: 2024-01-30
• 07290117772416 - LUSTER Tip, Round: 2024-01-30
• 17290117772420 - OPT™ Shields: 2024-01-03
• 07290117771372 - AcuPulse: 2023-12-12