Vari-Lase® Platinum Bright Tip laser fiber

GUDID M20671520

The VARI-LASE Platinum Bright Tip laser fiber is indicated for the treatment of varicose veins and varicosities associated with superficial reflux of the great saphenous vein and for the treatment of incompetence and reflux of superficial veins in the lower extremity.

Vascular Solutions, Inc.

Varicose vein lasing procedure kit

• Primary Device ID: M20671520
• NIH Device Record Key: 43da1e96-5201-4064-9876-6fe19a74cd1b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vari-Lase® Platinum Bright Tip laser fiber
• Version Model Number: 7152
• 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

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M20671520 [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