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 
 4 
 > 
 
33 records meeting your search criteria returned- Product Code: DSI Product Problem: Patient-Device Incompatibility Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH INTELLIVUE MP50 04/05/2023
PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH INTELLIVUE MX800 PATIENT MONITOR 04/05/2023
PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH INTELLIVUE MP70 04/04/2023
BRAEMAR MANUFACTURING, LLC BIOTEL HEART UNIVERSAL ELECTRODE PATCH 03/21/2023
BRAEMAR MANUFACTURING, LLC BIOTEL HEART UNIVERSAL ELECTRODE PATCH 03/10/2023
BRAEMAR MANUFACTURING, LLC C6 MCOT UNIVERSAL PATCH 02/17/2023
BRAEMAR MANUFACTURING, LLC C6 MCOT UNIVERSAL PATCH 02/14/2023
BRAEMAR MANUFACTURING, LLC UNIVERSAL ELECTRODE PATCH, 2CH 01/10/2023
BRAEMAR MANUFACTURING, LLC E-PATCH V 2.0 UNIVERSAL PATCH 09/18/2022
BRAEMAR MANUFACTURING, LLC E-PATCH V 2.0 UNIVERSAL PATCH 09/16/2022
-
-