Alma LipoFlow System 50Hz AALP24091501

GUDID 17290110121430

ALMA LASERS LTD.

Liposuction system Liposuction system

• Primary Device ID: 17290110121430
• NIH Device Record Key: 03946d0e-ffb1-4296-bc30-3785a71a0322
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Alma LipoFlow System 50Hz
• Version Model Number: 1
• Catalog Number: AALP24091501
• 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: 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	17290110121430 [Primary]

FDA Product Code

• MUU: System, Suction, Lipoplasty

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-08-23
• Device Publish Date: 2017-07-25

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