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
 

 
 
 1 
 2 
 3 
 > 
 
24 records meeting your search criteria returned- Product Code: DRM Patient Problem: Laceration(s) Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZOLL CIRCULATION AUTOPULSE RESUSCITATION MODEL 100 03/01/2023
ZOLL CIRCULATION AUTOPULSE® LIFEBAND 03/01/2023
JOLIFE AB - 3005445717 UNKNOWN_MEDICAL - LUND_PRODUCT 01/25/2023
JOLIFE AB - 3005445717 LUCAS 3, 3.1, IN SHIPPING BOX, EN 01/25/2023
JOLIFE AB - 3005445717 LUCAS ® CPR CHEST COMPRESSION SYSTEM 01/24/2023
JOLIFE AB - 3005445717 LUCAS¿ CPR CHEST COMPRESSION SYSTEM 01/23/2023
JOLIFE AB - 3005445717 LUCAS 2, 2.2, IN SHIPPING BOX,EN,DA,SV,F 01/23/2023
JOLIFE AB - 3005445717 LUCAS 3 CHEST COMPRESSION SYSTEM 01/20/2023
JOLIFE AB - 3005445717 LUCAS¿ CPR CHEST COMPRESSION SYSTEM 01/17/2023
JOLIFE AB - 3005445717 LUCAS ® CPR CHEST COMPRESSION SYSTEM 01/10/2023
-
-