• 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
ARJO HUNTLEIGH HOYER POWER LIFT 11/16/2016
ARJOHUNTLEIGH MAGOG INC. MAXI MOVE 11/14/2016
ARJOHUNTLEIGH MAGOG INC. MAXI MOVE 11/02/2016
ARJOHUNTLEIGH MAGOG INC. MAXI SKY 600 11/01/2016
ARJOHUNTLEIGH MAGOG INC. MAXI 500 10/29/2016
MEDIBO MEDICAL PRODUCTS NV ENCORE 10/21/2016
ARJOHUNTLEIGH MAGOG INC. MAXI MOVE 10/18/2016
ARJOHUNTLEIGH POLSKA SP. Z O.O. CONCERTO + BASIC 10/12/2016
H FINE & SONS LTD NA1629 ACCESS SLING WITH HEAD SUPPORT 09/30/2016
ARJOHUNTLEIGH POLSKA SP. Z O.O. TENOR 08/26/2016
-
-