Vari-Lase® Flex laser fiber and procedure kits

GUDID M20671651

Varicose vein lasing procedure kit

Primary Device ID	M20671651
NIH Device Record Key	7a643762-603d-49f3-9235-836ed56120f2
Commercial Distribution Discontinuation	2022-11-18
Commercial Distribution Status	Not in Commercial Distribution
Brand Name	Vari-Lase® Flex laser fiber and procedure kits
Version Model Number	7165
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	true
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

Device Issuing Agency	Device ID
HIBCC	M20671651 [Primary]

GEX	Powered Laser Surgical Instrument

Steralize Prior To Use	false
Device Is Sterile	true

M20671661	The VARI-LASE Platinum Bright Tip laser fiber is indicated for the treatment of varicose veins a
M20671631	The VARI-LASE Platinum Bright Tip laser fiber is indicated for the treatment of varicose veins a
M20671671	The VARI-LASE Platinum Bright Tip laser fiber is indicated for the treatment of varicose veins a
M20671651	The VARI-LASE Platinum Bright Tip laser fiber is indicated for the treatment of varicose veins a
M20671641	The VARI-LASE Platinum Bright Tip laser fiber is indicated for the treatment of varicose veins a

Mark Image Registration \| Serial	Company Trademark Application Date
VARI-LASE 78217901 2846854 Live/Registered	TELEFLEX INNOVATIONS S.Ã R.L. 2003-02-23