• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

  • 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 
 > 
 
41 records meeting your search criteria returned- Product Code: FQO Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
STERIS CORPORATION - MONTGOMERY ARMBOARD WITH GRAVITY LATCH 11/08/2019
STERIS CORPORATION - MONTGOMERY 4085 SURGICAL TABLE 09/20/2019
STERIS CORPORATION - MONTGOMERY 5085 SURGICAL TABLE 09/11/2019
STERIS CORPORATION - MONTGOMERY ARMBOARD WITH GRAVITY LATCH 07/01/2019
HOLGER ULLRICH ALPHAMAXX MOTOR DRIVE UNIT, EU SIDE RAIL 05/06/2019
STERIS CORPORATION - MONTGOMERY 5085 SURGICAL TABLE 05/03/2019
HOLGER ULLRICH SPECIAL PURPOSE OP-TABLE TOP 03/20/2019
HOLGER ULLRICH ALPHASTAR PRO, EU, SFC, LOW 03/05/2019
HOLGER ULLRICH MEERA EU WITHOUT AUTO DRIVE 02/22/2019
STERIS CORPORATION - MONTGOMERY ARMBOARD WITH GRAVITY LATCH 01/09/2019
-
-