• 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
 

 
 < 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 > 
 
315 records meeting your search criteria returned- Product Code: KDI Product Problem: Break Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BAXTER HEALTHCARE CORPORATION PRISMAFLEX HF1000 06/18/2021
BAXTER HEALTHCARE CORPORATION PRISMAFLEX 06/15/2021
BAXTER HEALTHCARE CORPORATION PRISMAFLEX M150 06/08/2021
BAXTER HEALTHCARE CORPORATION PRISMAFLEX M100 06/07/2021
BAXTER HEALTHCARE CORPORATION AK 96 06/01/2021
BAXTER HEALTHCARE CORPORATION PRISMAFLEX ST150 05/26/2021
BAXTER HEALTHCARE CORPORATION PRISMAFLEX M150 05/25/2021
BAXTER HEALTHCARE CORPORATION SEPXIRIS 150 05/17/2021
BAXTER HEALTHCARE CORPORATION PRISMAFLEX 05/04/2021
BAXTER HEALTHCARE CORPORATION PRISMAFLEX M100 05/04/2021
-
-