• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 
7 records meeting your search criteria returned- Product Code: DWF Patient Problem: Sepsis Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CARDIACASSIST INC. PROTEK DUO VENO-VENOUS CANNULA 08/07/2023
CARDIACASSIST INC. PROTEK DUO VENO-VENOUS CANNULA 08/04/2022
MEDTRONIC MEXICO S. DE R.L. DE CV CUSTOM TUBING PACK 03/09/2021
MEDTRONIC MEXICO S. DE R.L. DE CV CUSTOM TUBING PACK 03/03/2021
MEDTRONIC MEXICO S. DE R.L. DE CV CUSTOM TUBING PACK 03/03/2021
PERFUSION SYSTEMS BIO-MEDICUS NG 23 FR ARTERIAL CANNULA 10/21/2020
PERFUSION SYSTEMS BIO-MEDICUS NG 15 FR ARTERIAL CANNULA 10/21/2020
-
-