• 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
 

 
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
229 records meeting your search criteria returned- Product Code: KDI Patient Problem: Death Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
NXSTAGE MEDICAL, INC. NXSTAGE SYSTEM ONE 02/03/2021
CONCORD MANUFACTURING 2008T HEMODIALYSIS SYS., WITH CDX 01/29/2021
CONCORD MANUFACTURING 2008T HEMODIALYSIS SYS., WITH CDX 01/29/2021
NXSTAGE MEDICAL, INC. NXSTAGE SYSTEM ONE 01/15/2021
OUTSET MEDICAL, INC. TABLO HEMODIALYSIS SYSTEM 01/13/2021
OUTSET MEDICAL, INC. TABLO HEMODIALYSIS SYSTEM 01/10/2021
BAXTER HEALTHCARE CORPORATION PRISMAFLEX 01/05/2021
BAXTER HEALTHCARE CORPORATION PHOENIX 01/04/2021
BAXTER HEALTHCARE CORPORATION PRISMAFLEX ST150 12/30/2020
CONCORD MANUFACTURING 2008K2 HEMODIALYSIS SYS. OLC/DIASAFE PLS 12/23/2020
-
-