ClearLift AAQS24102208

GUDID 07290110123468

ALMA LASERS LTD.

Multi-modality skin surface treatment system

• Primary Device ID: 07290110123468
• NIH Device Record Key: f89f0c80-d6f2-480d-b0e9-c1b5275338c2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ClearLift
• Version Model Number: 1
• Catalog Number: AAQS24102208
• Company DUNS: 532283264
• Company Name: ALMA LASERS 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290110123468 [Primary]

FDA Product Code

• GEX: Powered Laser Surgical Instrument

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: 2024-02-26
• Device Publish Date: 2024-02-18

Devices Manufactured by ALMA LASERS LTD.

• 07290110123567 - Alma TED System 120V 50/60HZ: 2024-09-23 Alma TED System 120V 50/60HZ
• 07290110123611 - TED Applicator: 2024-09-23 TED Applicator
• 17290110123526 - Diode 755nm Alex Applicator for Soprano Titanium (Black): 2024-03-25 Diode 755nm Alex Applicator for Soprano Titanium (Black)
• 07290110123451 - ClearVas: 2024-02-26
• 07290110123468 - ClearLift: 2024-02-26
• 07290110123468 - ClearLift: 2024-02-26
• 07290110123475 - Alma SupErb: 2024-02-26
• 07290110123482 - ClearSkin: 2024-02-26
• 07290110123444 - NIR Face (6) HP: 2024-02-07