FemiLift Smart Protector AACO29031574

GUDID 17290110122000

ALMA LASERS LTD.

Multi-modality skin surface treatment system

• Primary Device ID: 17290110122000
• NIH Device Record Key: 67a8f96f-2017-48a6-9de1-89422444bdc9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FemiLift Smart Protector
• Version Model Number: 1
• Catalog Number: AACO29031574
• 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: true
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: true
• 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	17290110122000 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K103501

FDA Product Code

• HQF: Laser, Ophthalmic

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: 2020-12-31
• Device Publish Date: 2020-12-23

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