Vari-Lase® Platinum Bright Tip laser fiber

GUDID M20671460

Vascular Solutions, Inc.

Varicose vein lasing procedure kit

• Primary Device ID: M20671460
• NIH Device Record Key: 0c4f62c8-7808-4ed7-aed8-8af1b1018d14
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vari-Lase® Platinum Bright Tip laser fiber
• Version Model Number: 7146
• Company DUNS: 008999906
• Company Name: Vascular Solutions, Inc.
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 888-240-6001
• Email: customerservice@vasc.com

Device Dimensions

• Length: 250 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M20671460 [Primary]

FDA Product Code

• GEX: Powered Laser Surgical Instrument

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-11-11
• Device Publish Date: 2016-09-05

On-Brand Devices [Vari-Lase® Platinum Bright Tip laser fiber]

• M20671520: The VARI-LASE Platinum Bright Tip laser fiber is indicated for the treatment of varicose veins a
• M20671480: The VARI-LASE Platinum Bright Tip laser fiber is indicated for the treatment of varicose veins a
• M20671460: 7146