| 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 |