• 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 
 4 
 > 
 
37 records meeting your search criteria returned- Product Code: DRM Product Problem: Material Split, Cut or Torn Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZOLL CIRCULATION INC AUTOPULSE® LIFEBAND 01/15/2024
ZOLL CIRCULATION INC AUTOPULSE® LIFEBAND 08/28/2023
ZOLL CIRCULATION INC AUTOPULSE® LIFEBAND 08/28/2023
ZOLL CIRCULATION INC AUTOPULSE® LIFEBAND 08/28/2023
ZOLL CIRCULATION AUTOPULSE® LIFEBAND 04/18/2023
ZOLL CIRCULATION AUTOPULSE® LIFEBAND 04/18/2023
ZOLL CIRCULATION AUTOPULSE® LIFEBAND 03/27/2023
ZOLL CIRCULATION AUTOPULSE® LIFEBAND 02/17/2023
ZOLL CIRCULATION AUTOPULSE® LIFEBAND 01/06/2023
ZOLL CIRCULATION INC AUTOPULSE® LIFEBAND 10/05/2022
-
-