• 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 
 
 
29 records meeting your search criteria returned- Product Code: FQH Product Problem: Material Rupture Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC ACCUMIST BLOWER/MISTER 08/14/2017
ZIMMER SURGICAL, INC. COMPONENT KIT 01/09/2017
ZIMMER SURGICAL, INC. HIP KIT 08/15/2016
ZIMMER SURGICAL, INC. PULSAVAC PLUS WOUND DEBRIDEMENT SYSTEM F 11/18/2015
ZIMMER SURGICAL, INC. FAN SPRAY KIT 10/26/2015
ZIMMER SURGICAL, INC. PULSAVAC PLUS WOUND DEBRIDEMENT SYSTEM H 10/15/2015
ZIMMER SURGICAL PULSAVAC PLUS WOUND DEBRIDEMENT SYSTEM H 07/01/2015
ZIMMER SURGICAL PULSAVAC PLUS WOUND DEBRIDEMENT SYSTEM F 01/07/2015
ZIMMER SURGICAL PULSAVAC PLUS WOUND DEBRIDEMENT SSYTEM F 09/04/2014
-
-