PuraStat 621-062

GUDID 04560436590354

3-D MATRIX EUROPE

Synthetic peptide haemostatic agent
Primary Device ID04560436590354
NIH Device Record Keyacc57dec-6181-430b-9c97-61821e14421d
Commercial Distribution StatusIn Commercial Distribution
Brand NamePuraStat
Version Model Number621-035
Catalog Number621-062
Company DUNS264081545
Company Name3-D MATRIX EUROPE
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS104560436590354 [Primary]

FDA Product Code

QAUHemostatic Device For Endoscopic Gastrointestinal Use

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-03-11
Device Publish Date2025-03-03

Trademark Results [PuraStat]

Mark Image

Registration | Serial
Company
Trademark
Application Date
PURASTAT
PURASTAT
79255887 not registered Live/Pending
Advanced Skin Technology Pty Ltd
2019-02-28
PURASTAT
PURASTAT
79104216 4216013 Live/Registered
3-D Matrix, Ltd.
2011-07-14
PURASTAT
PURASTAT
73548759 1382912 Dead/Cancelled
PURAFIL, INC.
1985-07-18

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