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 
 > 
 
97 records meeting your search criteria returned- Product Code: FSA Product Problem: Device Handling Problem Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ARJOHUNTLEIGH POLSKA SP. Z O.O. CALYPSO 10/25/2017
ARJOHUNTLEIGH MAGOG INC. ERGOLIFT 10/12/2017
ARJOHUNTLEIGH MAGOG INC. MAXI 500 10/09/2017
SUNRISE MEDICAL HOYER 09/25/2017
ARJOHUNTLEIGH MAGOG INC. MAXI 500 09/25/2017
ARJOHUNTLEIGH MAGOG INC. MAXI MOVE 09/22/2017
ARJO HOSPITAL EQUIPMENT AB CONCERTO + BASIC 09/01/2017
ARJOHUNTLEIGH POLSKA SP Z O.O MINSTREL 08/02/2017
ARJOHUNTLEIGH POLSKA SP. Z O.O. SARA 3000 07/07/2017
APEX HEALTHCARE MFG INC HOYER PRESENCE LIFT 07/03/2017
-
-