• 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
 

 
 
10 records meeting your search criteria returned- Product Code: KDI Product Problem: Occlusion Within Device Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
OGDEN MANUFACTURING PLANT OPTIFLUX 160NRE DIALYZER FINISHED ASSY. 06/26/2018
NXSTAGE MEDICAL, INC. NXSTAGE SYSTEM ONE 12/20/2017
OGDEN MANUFACTURING PLANT OPTIFLUX 180NRE DIALYZER FINISHED ASSY. 10/25/2017
FRESENIUS MEDICAL CARE NORTH AMERICA OPTIFLUX 180NR DIALYZER FINISHED ASSMBLY 08/19/2016
FRESENIUS MEDICAL CARE NORTH AMERICA 2008K2 HEMODIALYSIS SYS. OLC/DIASAFE PLS 06/30/2016
FRESENIUS MEDICAL CARE NORTH AMERICA OPTIFLUX 160NRE DIALYZER FINISHED ASSY. 06/21/2016
FRESENIUS MEDICAL CARE NORTH AMERICA 2008T HEMODIALYSIS SYS., WITH CDX 04/27/2016
NXSTAGE MEDICAL, INC. NXSTAGE SYSTEM ONE 03/21/2016
NIPRO CORP. (ODATE) NIPRO ELISIO DIALYZER 09/24/2015
NIPRO CORP. (ODATE) NIPRO ELISIO DIALYZER 09/24/2015
-
-