• 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
 

 
 
 1 
 2 
 > 
 
19 records meeting your search criteria returned- Product Code: MHX Patient Problem: Itching Sensation Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ZOLL MANUFACTURING CORPORATION ARRHYTHMIA MANAGEMENT SYSTEM 02/15/2023
ZOLL MANUFACTURING CORPORATION ARRHYTHMIA MANAGEMENT SYSTEM 02/13/2023
ZOLL MANUFACTURING CORPORATION UCOR HEART FAILURE AND ARRHYTHMIA MANAGE 12/29/2022
ZOLL MANUFACTURING CORPORATION UCOR HEART FAILURE AND ARRHYTHMIA MANAGE 12/15/2022
ZOLL MANUFACTURING CORPORATION ARRHYTHMIA MANAGEMENT SYSTEM 12/02/2022
ZOLL MANUFACTURING CORPORATION ARRHYTHMIA MANAGEMENT SYSTEM 11/10/2022
ZOLL MANUFACTURING CORPORATION ARRHYTHMIA MANAGEMENT SYSTEM 10/26/2022
ZOLL MANUFACTURING CORPORATION ARRHYTHMIA MANAGEMENT SYSTEM 10/12/2022
ZOLL MANUFACTURING CORPORATION ARRHYTHMIA MANAGEMENT SYSTEM 09/30/2022
ZOLL MANUFACTURING CORPORATION ARRHYTHMIA MANAGEMENT SYSTEM 09/08/2022
-
-