Tip ClearLift QS CVD (Female) AACL02062120

GUDID 17290110122246

ALMA LASERS LTD.

Multi-modality skin surface treatment system

• Primary Device ID: 17290110122246
• NIH Device Record Key: f096b1ef-cff7-4680-bd0a-81e17f20cecd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Tip ClearLift QS CVD (Female)
• Version Model Number: 1
• Catalog Number: AACL02062120
• 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: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	17290110122246 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K072564

FDA Product Code

• FTC: Light, Ultraviolet, Dermatological

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: 2022-01-07
• Device Publish Date: 2021-12-30

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