Liposonix P006392-03

GUDID 00816995020141

INSTALLATION KIT, MODEL 2, GENERIC, P2.1

SOLTA MEDICAL

Ultrasonic body contouring system Ultrasonic body contouring system Ultrasonic body contouring system

• Primary Device ID: 00816995020141
• NIH Device Record Key: 6799a0b0-9c3c-49ac-b7f0-93fc27bf086b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Liposonix
• Version Model Number: P006392-03
• Catalog Number: P006392-03
• Company DUNS: 079999584
• Company Name: SOLTA MEDICAL
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00816995020141 [Primary]

FDA Product Code

• OHV: Focused Ultrasound For Tissue Heat Or Mechanical Cellular Disruption

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-11-05
• Device Publish Date: 2016-09-23

On-Brand Devices [Liposonix]

• 00816995020219: SYSTEM, WIFI, LIPOSONIX, P2.1.1
• 00816995020202: ASSEMBLY, HANDPIECE, P2.X
• 00816995020196: HANDPIECE, REPLACEMENT, P2.X
• 00816995020189: TREATMENT KIT, 1.3CM, WORLDWIDE
• 00816995020172: TREATMENT KIT,EXT. USE, 1.3CM, WORLDWIDE
• 00816995020158: CARTRIDGE, REPLACEABLE TREATMENT
• 00816995020141: INSTALLATION KIT, MODEL 2, GENERIC, P2.1