• 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 
 
 
27 records meeting your search criteria returned- Product Code: KDI Product Problem: Air/Gas in Device Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BAXTER HEALTHCARE CORPORATION PRISMAFLEX M150 05/11/2021
BAXTER HEALTHCARE CORPORATION THERANOVA 400 05/11/2021
BAXTER HEALTHCARE CORPORATION THERANOVA 400 05/06/2021
NXSTAGE MEDICAL, INC. NXSTAGE SYSTEM ONE 04/30/2021
BAXTER HEALTHCARE - MEYZIEU PRISMAFLEX M150 04/28/2021
BAXTER HEALTHCARE CORPORATION PRISMAFLEX M100 SET 03/16/2021
BAXTER HEALTHCARE CORPORATION PRISMAFLEX ST150 03/03/2021
-
-