Thrombi-Pad™ 3x3 hemostatic pad
GUDID M20609161
Vascular Solutions, Inc.
Thrombin haemostatic agent, non-antimicrobial Thrombin haemostatic agent, non-antimicrobial Thrombin haemostatic agent, non-antimicrobial Thrombin haemostatic agent, non-antimicrobial Thrombin haemostatic agent, non-antimicrobial Thrombin haemostatic agent, non-antimicrobial Thrombin haemostatic agent, non-antimicrobial Thrombin haemostatic agent, non-antimicrobial Thrombin haemostatic agent, non-antimicrobial Thrombin haemostatic agent, non-antimicrobial Thrombin haemostatic agent, non-antimicrobial Thrombin haemostatic agent, non-antimicrobial Thrombin haemostatic agent, non-antimicrobial Thrombin haemostatic agent, non-antimicrobial Thrombin haemostatic agent, non-antimicrobial Thrombin haemostatic agent, non-antimicrobial Thrombin haemostatic agent, non-antimicrobial Thrombin haemostatic agent, non-antimicrobial Thrombin haemostatic agent, non-antimicrobial Thrombin haemostatic agent, non-antimicrobial Thrombin haemostatic agent, non-antimicrobial Thrombin haemostatic agent, non-antimicrobial Thrombin haemostatic agent, non-antimicrobial Thrombin haemostatic agent, non-antimicrobial Thrombin haemostatic agent, non-antimicrobial Thrombin haemostatic agent, non-antimicrobial| Primary Device ID | M20609161 |
| NIH Device Record Key | 12d54cd1-91c6-41d2-89fb-234248a8a02d |
| Commercial Distribution Discontinuation | 2022-03-10 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Thrombi-Pad™ 3x3 hemostatic pad |
| Version Model Number | 0916 |
| 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 |
Customer Support Contacts
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | M20609160 [Primary] |
| HIBCC | M20609161 [Package] Contains: M20609160 Package: Box [10 Units] Discontinued: 2022-03-10 In Commercial Distribution |
FDA Product Code
| FRO | Dressing, Wound, Drug |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2020-12-11 |
| Device Publish Date | 2016-09-15 |
Devices Manufactured by Vascular Solutions, Inc.
| 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 |
Trademark Results [Thrombi-Pad]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 THROMBI-PAD 77103110 3550781 Live/Registered |
KING PHARMACEUTICALS RESEARCH AND DEVELOPMENT, LLC 2007-02-08 |
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