| Primary Device ID | M20630001 |
| NIH Device Record Key | e6eef221-f567-492b-9dd6-9210c3dfc682 |
| Commercial Distribution Discontinuation | 2023-11-08 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | D-Stat® Dry topical hemostat |
| Version Model Number | 3000 |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | M20630000 [Primary] |
| HIBCC | M20630001 [Package] Contains: M20630000 Package: Box [10 Units] Discontinued: 2023-11-08 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 |
| M20630011 | 3001 |
| M20630001 | 3000 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() D-STAT 78334412 3046850 Live/Registered |
FASHION SEAL CORP. 2003-12-01 |
![]() D-STAT 78102841 2754442 Live/Registered |
TELEFLEX INNOVATIONS S.Ã R.L. 2002-01-15 |
![]() D-STAT 74058739 1662942 Dead/Cancelled |
ION SYSTEMS, INC. 1990-05-14 |