| Primary Device ID | 04560436590354 |
| NIH Device Record Key | acc57dec-6181-430b-9c97-61821e14421d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PuraStat |
| Version Model Number | 621-035 |
| Catalog Number | 621-062 |
| Company DUNS | 264081545 |
| Company Name | 3-D MATRIX EUROPE |
| 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 |
|---|---|
| GS1 | 04560436590354 [Primary] |
| QAU | Hemostatic Device For Endoscopic Gastrointestinal Use |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-03-11 |
| Device Publish Date | 2025-03-03 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PURASTAT 79255887 not registered Live/Pending |
Advanced Skin Technology Pty Ltd 2019-02-28 |
![]() PURASTAT 79104216 4216013 Live/Registered |
3-D Matrix, Ltd. 2011-07-14 |
![]() PURASTAT 73548759 1382912 Dead/Cancelled |
PURAFIL, INC. 1985-07-18 |