• 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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 > 
 
381 records meeting your search criteria returned- Product Code: KDI Patient Problem: Blood Loss Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BAXTER HEALTHCARE CORPORATION PRISMAX 03/19/2020
GAMBRO RENAL PRODUCTS, INC. REVACLEAR 03/19/2020
BAXTER HEALTHCARE - HECHINGEN BADEN DIAL POLYFLUX 210H 03/03/2020
OGDEN MANUFACTURING PLANT OPTIFLUX 160NRE DIALYZER FINISHED ASSY. 02/27/2020
OGDEN MANUFACTURING PLANT DIALYZER 02/27/2020
BAXTER HEALTHCARE CORPORATION PRISMAX 02/18/2020
FRESENIUS MEDICAL CARE HOLDINGS, INC. OPTIFLUX® 02/14/2020
OUTSET MEDICAL, INC. TABLO HEMODIALYSIS SYSTEM 02/10/2020
NXSTAGE MEDICAL, INC. NXSTAGE SYSTEM ONE 02/04/2020
CONCORD MANUFACTURING 2008K HEMODIALYSIS SYS. OLC/DP, SPANISH 01/20/2020
-
-