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
 

 
 < 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 > 
 
105 records meeting your search criteria returned- Product Code: DRM Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
JOLIFE AB - 3005445717 LUCAS¿ CPR CHEST COMPRESSION SYSTEM 08/15/2019
PHYSIO-CONTROL, INC. - 3015876 LUCAS 3, 3.1, IN SHIPPING BOX, EN 08/15/2019
JOLIFE AB/ PHYSIO-CONTROL, INC. LUCAS DEVICE CPR 07/15/2019
JOLIFE AB - 3005445717 LUCAS 2 CPR CHEST COMPRESSION SYSTEM 05/07/2019
JOLIFE AB - 3005445717 LUCAS 2 CPR CHEST COMPRESSION SYSTEM 05/07/2019
PHYSIO-CONTROL, INC. - 3015876 LUCAS¿ CPR CHEST COMPRESSION SYSTEM 05/01/2019
ZOLL CIRCULATION INC AUTOPULSE® RESUSCITATION MODEL 100 04/30/2019
ZOLL CIRCULATION AUTOPULSE® LIFEBAND 04/30/2019
ZOLL CIRCULATION INC AUTOPULSE® RESUSCITATION MODEL 100 04/23/2019
ZOLL CIRCULATION INC AUTOPULSE® RESUSCITATION MODEL 100 04/19/2019
-
-