• 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
 

 
 < 
 9 
 10 
 11 
 12 
 13 
 14 
 
 
139 records meeting your search criteria returned- Product Code: GEI Product Problem: Patient Device Interaction Problem Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ETHICON ENDO-SURGERY, LLC. ENSEAL GENERIC PRODUCT CODE 04/27/2020
MEGADYNE MEDICAL PRODUCTS, INC. RTN ELEC DUAL PLATE 9FT CORD 04/01/2020
APPLIED MEDICAL RESOURCES UNKNOWN 03/10/2020
APPLIED MEDICAL RESOURCES EB015, VOYANT MARYLAND FUSION 37CM, 6/BX 03/02/2020
CONSOLIDATED MEDICAL EQUIPMENT MACROLYTE, AD, SINGLE, CABLE DISPERSIVE 02/24/2020
APPLIED MEDICAL RESOURCES EB015, VOYANT MARYLAND FUSION 37CM, 6/BX 12/27/2019
APPLIED MEDICAL RESOURCES EB030, VOYANT FINE FUSION, 6/BX 09/30/2019
CONSOLIDATED MEDICAL EQUIPMENT SUREFIT GROUNDING PAD 02/06/2019
ERBE ELEKTROMEDIZIN GMBH ERBE APC 2 01/08/2019
-
-