Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)
  • 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
 

 
 < 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 > 
 
121 records meeting your search criteria returned- Product Code: DTZ Patient Problem: Hemorrhage/Bleeding Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
PERFUSION SYSTEMS FUSION HOLLOW FIBER OXYGENATOR 09/13/2022
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO STERILE FX25REC W/RES 09/12/2022
PERFUSION SYSTEMS FUSION HOLLOW FIBER OXYGENATOR 09/07/2022
TERUMO CORPORATION, ASHITAKA CAPIOX FX25 OXYGENATOR 08/19/2022
PERFUSION SYSTEMS CARMEDA AFFINITY NT HOLLOW FIBER OXYGENA 08/05/2022
PERFUSION SYSTEMS FUSION HOLLOW FIBER OXYGENATOR 08/02/2022
MEDTRONIC MEXICO MEDTRONIC TUBING PACK 07/28/2022
PERFUSION SYSTEMS AFFINITY PIXIE PEDIATRIC HOLLOW FIBER OX 07/21/2022
PERFUSION SYSTEMS FUSION HOLLOW FIBER OXYGENATOR 06/17/2022
PERFUSION SYSTEMS FUSION HOLLOW FIBER OXYGENATOR 06/10/2022
-
-