• 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 
 > 
 
19 records meeting your search criteria returned- Product Code: DRM Patient Problem: Liver Laceration(s) Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
JOLIFE AB - 3005445717 LUCAS¿ 2 CPR CHEST COMPRESSION SYSTEM 02/15/2024
ZOLL CIRCULATION AUTOPULSE RESUSCITATION MODEL 100 08/30/2023
JOLIFE AB - 3005445717 LUCAS 2, 2.2, IN SHIPPING BOX,EN,DA,SV,F 01/25/2023
JOLIFE AB - 3005445717 LUCAS¿ CPR CHEST COMPRESSION SYSTEM 01/23/2023
JOLIFE AB - 3005445717 LUCAS¿ CPR CHEST COMPRESSION SYSTEM 01/17/2023
JOLIFE AB - 3005445717 LUCAS¿ CPR CHEST COMPRESSION SYSTEM 06/02/2022
PHYSIO-CONTROL, INC. - 3015876 UNKNOWN_MEDICAL - LUND_PRODUCT 07/01/2020
PHYSIO-CONTROL, INC. - 3015876 LUCAS CPR CHEST COMPRESSION SYSTEM 07/01/2020
JOLIFE AB - 3005445717 LUCAS ® CPR CHEST COMPRESSION SYSTEM 03/27/2020
JOLIFE AB - 3005445717 LUCAS ® CPR CHEST COMPRESSION SYSTEM 03/26/2020
-
-