DS applicator AS00099

GUDID 07290109950020

Elos-DS Applicator

SYNERON MEDICAL LTD

Multi-modality skin surface treatment system

• Primary Device ID: 07290109950020
• NIH Device Record Key: dad7695a-92e1-4a12-853a-1c37452caafe
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DS applicator
• Version Model Number: AS00099
• Catalog Number: AS00099
• 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

Customer Support Contacts

• Phone: 1.866.259.6661
• Email: info@Syneron-Candela.com
• Phone: 1.866.259.6661
• Email: info@Syneron-Candela.com
• Phone: 1.866.259.6661
• Email: info@Syneron-Candela.com
• Phone: 1.866.259.6661
• Email: info@Syneron-Candela.com
• Phone: 1.866.259.6661
• Email: info@Syneron-Candela.com
• Phone: 1.866.259.6661
• Email: info@Syneron-Candela.com
• Phone: 1.866.259.6661
• Email: info@Syneron-Candela.com
• Phone: 1.866.259.6661
• Email: info@Syneron-Candela.com
• Phone: 1.866.259.6661
• Email: info@Syneron-Candela.com
• Phone: 1.866.259.6661
• Email: info@Syneron-Candela.com
• Phone: 1.866.259.6661
• Email: info@Syneron-Candela.com
• Phone: 1.866.259.6661
• Email: info@Syneron-Candela.com
• Phone: 1.866.259.6661
• Email: info@Syneron-Candela.com
• Phone: 1.866.259.6661
• Email: info@Syneron-Candela.com
• Phone: 1.866.259.6661
• Email: info@Syneron-Candela.com
• Phone: 1.866.259.6661
• Email: info@Syneron-Candela.com
• Phone: 1.866.259.6661
• Email: info@Syneron-Candela.com
• Phone: 1.866.259.6661
• Email: info@Syneron-Candela.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290109950020 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K041969

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: 2016-09-20

On-Brand Devices [DS applicator]

• 07290109951997: DS Applicator, elos Plus
• 07290109951232: Elos-DS Applicator
• 07290109950020: Elos-DS Applicator