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

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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 
 
91 records meeting your search criteria returned- Product Code: DRM Product Problem: Device Inoperable Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZOLL CIRCULATION, INC AUTOPULSE® NIMH BATTERY 04/28/2014
ZOLL CIRCULATION, INC AUTOPULSE® LI-ION BATTERY 04/21/2014
ZOLL CIRCULATION, INC AUTOPULSE® LI-ION BATTERY 03/05/2014
ZOLL CIRCULATION, INC AUTOPULSE® LI-ION BATTERY 03/04/2014
ZOLL CIRCULATION, INC AUTOPULSE® RESUSCITATION SYSTEM MODEL 10 03/04/2014
ZOLL CIRCULATION, INC AUTOPULSE® LI-ION BATTERY 02/21/2014
ZOLL CIRCULATION, INC AUTOPULSE® RESUSCITATION SYSTEM MODEL 10 01/29/2014
ZOLL CIRCULATION, INC AUTOPULSE® RESUSCITATION SYSTEM MODEL 10 01/28/2014
MICHIGAN INSTRUMENTS, INC. LIFESTAT 01/28/2014
ZOLL CIRCULATION, INC AUTOPULSE® RESUSCITATION SYSTEM MODEL 10 01/24/2014
-
-