• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

  • 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 
 > 
 
164 records meeting your search criteria returned- Product Code: KDI Patient Problem: Blood Loss Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BAXTER HEALTHCARE CORPORATION DIALYZER, HIGH PERMEABILITY WITH OR WITH 07/26/2023
BAXTER HEALTHCARE CORPORATION PRISMAFLEX 02/17/2021
BAXTER HEALTHCARE CORPORATION PRISMAFLEX 02/07/2021
BAXTER HEALTHCARE CORPORATION PRISMAFLEX 02/07/2021
BAXTER HEALTHCARE CORPORATION PRISMAFLEX M60 02/07/2021
NXSTAGE MEDICAL, INC. NXSTAGE SYSTEM ONE 02/03/2021
BAXTER HEALTHCARE CORPORATION PRISMAX 02/01/2021
BAXTER HEALTHCARE CORP. PRISMAFLEX M100 FILTER SET CONTINUOUS DI 01/28/2021
BAXTER HEALTHCARE - MEYZIEU NI 01/27/2021
BAXTER HEALTHCARE CORPORATION PRISMAX 01/27/2021
-
-