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 
 > 
 
12 records meeting your search criteria returned- Product Code: FKJ Product Problem: Inadequate Ultra Filtration Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
B.BRAUN AVITUM AG DIALOG A +INCL. BIC 05/16/2017
B.BRAUN AVITUM AG DIALOG A +INCL. BIC 05/16/2017
B.BRAUN AVITUM AG DIALOG A +INCL. BIC 05/16/2017
B.BRAUN AVITUM AG DIALOG A +INCL. BIC 05/16/2017
B.BRAUN AVITUM AG DIALOG A +INCL. BIC 05/16/2017
B.BRAUN AVITUM AG DIALOG A +INCL. BIC 05/16/2017
B.BRAUN AVITUM AG DIALOG A +INCL. BIC 05/16/2017
B.BRAUN AVITUM AG DIALOG A +INCL. BIC 05/16/2017
B. BRAUN AVITUM AG - MELSUNGEN DIALOG A + HE/BIC 01/08/2016
B. BRAUN AVITUM AG - MELSUNGEN DIALOG A + HE/BIC 01/08/2016
-
-