Axis™ guidewire

GUDID M20673730

To facilitate the placement of devices during diagnostic and interventional procedures.

Vascular Solutions, Inc.

Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual
Primary Device IDM20673730
NIH Device Record Key9105fcd2-eac9-40ea-8cd9-26ac8be373a5
Commercial Distribution StatusIn Commercial Distribution
Brand NameAxis™ guidewire
Version Model Number7373
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 Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
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
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 Dimensions

Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter
Outer Diameter0.035 Inch
Length260 Centimeter

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM20673730 [Primary]
HIBCCM20673731 [Package]
Package: Box [5 Units]
In Commercial Distribution

FDA Product Code

DQXWire, Guide, Catheter

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2021-12-22
Device Publish Date2016-09-05

On-Brand Devices [Axis™ guidewire]

M20673740To facilitate the placement of devices during diagnostic and international procedures.
M20673730To facilitate the placement of devices during diagnostic and interventional procedures.
M20673720To facilitate the placement of devices during diagnostic and interventional procedures.
M20673710To facilitate the placement of devices during diagnostic and interventional procedures.
M206737007370

Trademark Results [Axis]

Mark Image

Registration | Serial
Company
Trademark
Application Date
AXIS
AXIS
98408491 not registered Live/Pending
ERCO GmbH
2024-02-16
AXIS
AXIS
98403895 not registered Live/Pending
Axis Legal Counsel PC
2024-02-13
AXIS
AXIS
98235434 not registered Live/Pending
Ortho Systems d/b/a Ovation Medical, Inc.
2023-10-23
AXIS
AXIS
98100213 not registered Live/Pending
Aperture, LLC
2023-07-25
AXIS
AXIS
97908211 not registered Live/Pending
AXIS GROUP VENTURES, LLC
2023-04-26
AXIS
AXIS
97878076 not registered Live/Pending
Nexcam, Inc.
2023-04-07
AXIS
AXIS
97822017 not registered Live/Pending
R & B South Sisters LLC
2023-03-03
AXIS
AXIS
97813960 not registered Live/Pending
ORIGIN Engineering LLC
2023-02-27
AXIS
AXIS
97720076 not registered Live/Pending
Milwaukee Electric Tool Corporation
2022-12-15
AXIS
AXIS
97720074 not registered Live/Pending
Milwaukee Electric Tool Corporation
2022-12-15
AXIS
AXIS
97620823 not registered Live/Pending
Vornado Air, LLC
2022-10-05
AXIS
AXIS
97562955 not registered Live/Pending
Norris, Justin, K
2022-08-24

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.