| Primary Device ID | M20673890 |
| NIH Device Record Key | 20d339bc-7d43-4096-b2e8-1048a51b79a2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Warrior™ guidewire |
| Version Model Number | 7389 |
| 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 |
| Phone | 888-240-6001 |
| customerservice@vasc.com | |
| Phone | 888-240-6001 |
| customerservice@vasc.com | |
| Phone | 888-240-6001 |
| customerservice@vasc.com | |
| Phone | 888-240-6001 |
| customerservice@vasc.com | |
| Phone | 888-240-6001 |
| customerservice@vasc.com | |
| Phone | 888-240-6001 |
| customerservice@vasc.com | |
| Phone | 888-240-6001 |
| customerservice@vasc.com | |
| Phone | 888-240-6001 |
| customerservice@vasc.com | |
| Phone | 888-240-6001 |
| customerservice@vasc.com | |
| Phone | 888-240-6001 |
| customerservice@vasc.com | |
| Phone | 888-240-6001 |
| customerservice@vasc.com | |
| Phone | 888-240-6001 |
| customerservice@vasc.com | |
| Phone | 888-240-6001 |
| customerservice@vasc.com | |
| Phone | 888-240-6001 |
| customerservice@vasc.com | |
| Phone | 888-240-6001 |
| customerservice@vasc.com |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | M20673890 [Primary] |
| DQX | Wire, Guide, Catheter |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-11-11 |
| Device Publish Date | 2018-03-07 |
| M20673890 | 7389 |
| M20673880 | 7388 |