• 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
 

 
 
10 records meeting your search criteria returned- Product Code: LDD Product Problem: No Display/Image Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SCHILLER AG TEMPUS LS-MANUAL 03/06/2023
SCHILLER AG TEMPUS LS-MANUAL 09/06/2022
PHILIPS MEDICAL SYSTEMS CODEMASTER XL 07/26/2016
PHILIPS MEDICAL SYSTEMS CODEMASTER XL 11/11/2015
PHILIPS MEDICAL SYSTEMS 43110A DEFIBRILLATOR/MONITOR 10/31/2014
ZOLL MEDICAL CORPORATION PROPAQ MD DEFIBRILLATOR 08/15/2014
PHILIPS MRX 06/04/2014
ZOLL MEDICAL CORPORATION PROPAQ MD DEFIBRILLATOR 03/21/2014
PHYSIO-CONTROL LIFE PACK 12 03/05/2014
PHILIPS MEDICAL SYSTEMS CODEMASTER XL+ 01/08/2014
-
-