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
 

 
 
8 records meeting your search criteria returned- Product Code: OEQ Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MERIT MEDICAL SYSTEMS INC. MERIT CUSTOM KIT 02/09/2023
MERIT MEDICAL SYSTEMS CUSTOM KIT 01/27/2022
MERIT MEDICAL SYSTEMS INC. HOPITAL DE HAUL LEVEQUE.BORDEAUX.. 12/03/2021
CORDIS CORPORATION UNKNOWN GUIDING CATHETER CARDIOLOGY 05/11/2021
CORDIS CORPORATION UNKNOWN GUIDING CATHETER CARDIOLOGY 05/10/2021
MERIT MEDICAL SYSTEMS INC. SPECTRANETICS BRIDGE BALLOON PREP KIT 01/07/2021
CAREFUSION, INC UNKNOWN CHLORAPREP 12/16/2020
CAREFUSION, INC UNKNOWN CHLORAPREP 12/09/2020
-
-