Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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 
 > 
 
175 records meeting your search criteria returned- Product Code: KDI Product Problem: Component Missing Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BAXTER HEALTHCARE CORPORATION REVACLEAR 10/16/2023
NXSTAGE MEDICAL INC. NXSTAGE 03/09/2022
BAXTER HEALTHCARE CORPORATION THERANOVA 500 01/21/2022
BAXTER HEALTHCARE CORPORATION PRISMAFLEX 02/11/2021
GAMBRO INDUSTRIES BAXTER PLASMAFLEX CRRT MEMBRANE 04/30/2020
MEDISYSTEMS / B. BRAUN MEDICAL INC. STREAMLINE AIRLESS SYSTEM FOR B BRAUN DI 12/19/2019
NXSTAGE MEDICAL, INC. NXSTAGE CARTRIDGE EXPRESS 06/13/2019
GAMBRO INDUSTRIES PRISMAFLEX HF1000 10/11/2018
GAMBRO INDUSTRIES PRISMAFLEX HF1000 10/11/2018
GAMBRO LUNDIA AB PRISMAFLEX 07/14/2016
-
-