SRA Plus applicator FG71141

GUDID 07290109950952

SRA Plus, Large Applicator, elos Plus

SYNERON MEDICAL LTD

Multi-modality skin surface treatment system

• Primary Device ID: 07290109950952
• NIH Device Record Key: c9c5507a-0c07-40f3-b2a2-cd66e041e22e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SRA Plus applicator
• Version Model Number: FG71141
• Catalog Number: FG71141
• 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	07290109950952 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K113868

FDA Product Code

• GEX: Powered Laser Surgical Instrument

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: 2016-09-21

On-Brand Devices [SRA Plus applicator]

• 07290109951843: SRA Plus, Large Applicator, elos Plus
• 07290109950952: SRA Plus, Large Applicator, elos Plus