VSI Radiofrequency Ablation Procedure Pack with 7F 7cm Micro-HV Kit

GUDID M20677960

Vascular Solutions, Inc.

General/plastic surgical procedure kit, non-medicated, single-use General/plastic surgical procedure kit, non-medicated, single-use General/plastic surgical procedure kit, non-medicated, single-use General/plastic surgical procedure kit, non-medicated, single-use General/plastic surgical procedure kit, non-medicated, single-use General/plastic surgical procedure kit, non-medicated, single-use General surgical procedure kit, non-medicated, single-use General surgical procedure kit, non-medicated, single-use General surgical procedure kit, non-medicated, single-use General surgical procedure kit, non-medicated, single-use General surgical procedure kit, non-medicated, single-use General surgical procedure kit, non-medicated, single-use General surgical procedure kit, non-medicated, single-use General surgical procedure kit, non-medicated, single-use General surgical procedure kit, non-medicated, single-use General surgical procedure kit, non-medicated, single-use General surgical procedure kit, non-medicated, single-use General surgical procedure kit, non-medicated, single-use General surgical procedure kit, non-medicated, single-use General surgical procedure kit, non-medicated, single-use General surgical procedure kit, non-medicated, single-use General surgical procedure kit, non-medicated, single-use General surgical procedure kit, non-medicated, single-use General surgical procedure kit, non-medicated, single-use
Primary Device IDM20677960
NIH Device Record Key75861d0e-5ba4-44be-9c13-4d75be16a836
Commercial Distribution StatusIn Commercial Distribution
Brand NameVSI Radiofrequency Ablation Procedure Pack with 7F 7cm Micro-HV Kit
Version Model Number7796
Company DUNS008999906
Company NameVascular Solutions, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone888-240-6001
Emailcustomerservice@vasc.com
Phone888-240-6001
Emailcustomerservice@vasc.com
Phone888-240-6001
Emailcustomerservice@vasc.com
Phone888-240-6001
Emailcustomerservice@vasc.com
Phone888-240-6001
Emailcustomerservice@vasc.com
Phone888-240-6001
Emailcustomerservice@vasc.com
Phone888-240-6001
Emailcustomerservice@vasc.com
Phone888-240-6001
Emailcustomerservice@vasc.com
Phone888-240-6001
Emailcustomerservice@vasc.com
Phone888-240-6001
Emailcustomerservice@vasc.com
Phone888-240-6001
Emailcustomerservice@vasc.com
Phone888-240-6001
Emailcustomerservice@vasc.com
Phone888-240-6001
Emailcustomerservice@vasc.com
Phone888-240-6001
Emailcustomerservice@vasc.com
Phone888-240-6001
Emailcustomerservice@vasc.com
Phone888-240-6001
Emailcustomerservice@vasc.com
Phone888-240-6001
Emailcustomerservice@vasc.com
Phone888-240-6001
Emailcustomerservice@vasc.com
Phone888-240-6001
Emailcustomerservice@vasc.com
Phone888-240-6001
Emailcustomerservice@vasc.com
Phone888-240-6001
Emailcustomerservice@vasc.com
Phone888-240-6001
Emailcustomerservice@vasc.com
Phone888-240-6001
Emailcustomerservice@vasc.com
Phone888-240-6001
Emailcustomerservice@vasc.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM20677960 [Primary]

FDA Product Code

DYBIntroducer, Catheter

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-11-11
Device Publish Date2016-09-06

Devices Manufactured by Vascular Solutions, Inc.

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M20677181 - Vascular Solutions Custom Access Kit2023-06-09 The Custom Access Kit is intended to introduce up to a 0.038”/0.89mm guidewire or catheter into the vascular system following
M20677191 - Vascular Solutions Custom Access Kit2023-06-09 The Custom Access Kit is intended to introduce up to a 0.038”/0.89mm guidewire or catheter into the vascular system following
M20677201 - Vascular Solutions Custom Access Kit2023-06-09 The Custom Access Kit is intended to introduce up to a 0.038”/0.89mm guidewire or catheter into the vascular system following
M20677211 - Vascular Solutions Custom Access Kit2023-06-09 The Custom Access Kit is intended to introduce up to a 0.038”/0.89mm guidewire or catheter into the vascular system following
M20677221 - Vascular Solutions Custom Access Kit2023-06-09 The Custom Access Kit is intended to introduce up to a 0.038”/0.89mm guidewire or catheter into the vascular system following
M20677231 - Vascular Solutions Custom Access Kit2023-06-09 The Custom Access Kit is intended to introduce up to a 0.038”/0.89mm guidewire or catheter into the vascular system following

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