Axis™ guidewire
GUDID M20673710
To facilitate the placement of devices during diagnostic and interventional procedures.
Vascular Solutions, Inc.
Peripheral vascular guidewire, manual| Primary Device ID | M20673710 |
| NIH Device Record Key | 5e9bdaab-bddc-493d-9428-d3705cc71eb1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Axis™ guidewire |
| Version Model Number | 7371 |
| 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 | false |
| 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
Device Dimensions
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
| Length | 90 Centimeter |
| Outer Diameter | 0.035 Inch |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | M20673710 [Primary] |
| HIBCC | M20673711 [Package] Package: Box [5 Units] In Commercial Distribution |
FDA Product Code
| DQX | Wire, Guide, Catheter |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2021-12-22 |
| Device Publish Date | 2016-09-05 |
On-Brand Devices [Axis™ guidewire]
| M20673740 | To facilitate the placement of devices during diagnostic and international procedures. |
| M20673730 | To facilitate the placement of devices during diagnostic and interventional procedures. |
| M20673720 | To facilitate the placement of devices during diagnostic and interventional procedures. |
| M20673710 | To facilitate the placement of devices during diagnostic and interventional procedures. |
| M20673700 | 7370 |
Trademark Results [Axis]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 AXIS 98859871 not registered Live/Pending |
AXIS Composites LLC 2024-11-18 |
 AXIS 98748873 not registered Live/Pending |
The Tiffen Company, LLC 2024-09-13 |
 AXIS 98625811 not registered Live/Pending |
Alexander Andrew, Inc. 2024-06-29 |
 AXIS 98408491 not registered Live/Pending |
ERCO GmbH 2024-02-16 |
 AXIS 98403895 not registered Live/Pending |
Axis Legal Counsel PC 2024-02-13 |
 AXIS 98235434 not registered Live/Pending |
Ortho Systems d/b/a Ovation Medical, Inc. 2023-10-23 |
 AXIS 98100213 not registered Live/Pending |
Aperture, LLC 2023-07-25 |
 AXIS 97908211 not registered Live/Pending |
AXIS GROUP VENTURES, LLC 2023-04-26 |
 AXIS 97878076 not registered Live/Pending |
Nexcam, Inc. 2023-04-07 |
 AXIS 97822017 not registered Live/Pending |
R & B South Sisters LLC 2023-03-03 |
 AXIS 97813960 not registered Live/Pending |
ORIGIN Engineering LLC 2023-02-27 |
 AXIS 97720076 not registered Live/Pending |
Milwaukee Electric Tool Corporation 2022-12-15 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.