• 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
 

 
 
7 records meeting your search criteria returned- Product Code: MOQ Product Problem: Use of Device Problem Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZOLL CIRCULATION AUTOPULSE® LI-ION BATTERY 12/05/2023
ZOLL CIRCULATION AUTOPULSE® LI-ION BATTERY 11/18/2022
ZIMMER SURGICAL SA ASEPTIC BATTERY HOUSING 07/07/2022
ZIMMER SURGICAL SA ASEPTIC BATTERY HOUSING 06/01/2022
ZIMMER SURGICAL SA ASEPTIC BATTERY HOUSING 05/11/2022
ZOLL CIRCULATION AUTOPULSE® LI-ION BATTERY 12/07/2021
ZOLL CIRCULATION AUTOPULSE® LI-ION BATTERY 09/30/2019
-
-