VelaShape III system FG71201

GUDID 07290109952031

VelaShape III System 120V, Packaged

SYNERON MEDICAL LTD

Multi-modality skin contouring system

• Primary Device ID: 07290109952031
• NIH Device Record Key: be476f83-2a6e-47aa-a192-6e77a18aee5d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VelaShape III system
• Version Model Number: FG71201
• Catalog Number: FG71201
• Company DUNS: 532685716
• Company Name: SYNERON MEDICAL 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: false
• 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	07290109952031 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K120510
• Premarket Notification: K122579

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

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: 2018-07-06
• Device Publish Date: 2016-09-25

On-Brand Devices [VelaShape III system]

• 07290109952031: VelaShape III System 120V, Packaged
• 07290109952024: VelaShape III System 100V, Packaged