• 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 
 > 
 
82 records meeting your search criteria returned- Product Code: KDI Patient Problem: Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BAXTER HEALTHCARE CORPORATION PRISMAX MACHINES 04/05/2022
BAXTER HEALTHCARE CORPORATION PRISMAFLEX TPE 03/31/2022
BAXTER HEALTHCARE CORPORATION NI 03/29/2022
BAXTER HEALTHCARE CORPORATION OXIRIS S 03/24/2022
BAXTER HEALTHCARE CORPORATION PRISMAFLEX SETS HF 03/19/2022
FRESENIUS USA, INC. 2008® SERIES HEMODIALYSIS MACHINES 03/17/2022
BAXTER HEALTHCARE CORPORATION PRISMAFLEX 03/17/2022
BAXTER HEALTHCARE CORPORATION PRISMAFLEX SETS M & ST 03/14/2022
BAXTER HEALTHCARE CORPORATION PRISMAX 03/09/2022
BAXTER HEALTHCARE CORPORATION PRISMAX 03/01/2022
-
-