| Primary Device ID | M20641501 |
| NIH Device Record Key | e4912af1-8004-4993-99e2-8fa1492114c7 |
| Commercial Distribution Discontinuation | 2023-06-23 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ThrombiDisc™ topical hemostat |
| Version Model Number | 4150 |
| 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 | |
| Phone | 888-240-6001 |
| customerservice@vasc.com | |
| Phone | 888-240-6001 |
| customerservice@vasc.com |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | M20641500 [Primary] |
| HIBCC | M20641501 [Package] Contains: M20641500 Package: Box [25 Units] Discontinued: 2023-06-23 In Commercial Distribution |
| FRO | Dressing, Wound, Drug |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2023-06-06 |
| Device Publish Date | 2016-09-15 |
| M20677101 - Vascular Solutions Custom Access Kit | 2023-06-09 |
| M20677141 - Vascular Solutions Custom Access Kit | 2023-06-09 The Custom Access Kit is intended to introduce up to a 0.038”/0.89mm guidewire or catheter into the vascular system following |
| M20677181 - Vascular Solutions Custom Access Kit | 2023-06-09 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 Kit | 2023-06-09 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 Kit | 2023-06-09 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 Kit | 2023-06-09 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 Kit | 2023-06-09 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 Kit | 2023-06-09 The Custom Access Kit is intended to introduce up to a 0.038”/0.89mm guidewire or catheter into the vascular system following |