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 |