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
 

 
 
9 records meeting your search criteria returned- Product Code: EYA Patient Problem: No Known Impact Or Consequence To Patient Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
EP FLEX 0.038" HYBRID WIRE, BOX OF 5 11/26/2019
EP FLEX 0.038" HYBRID WIRE, BOX OF 5 07/02/2019
GYRUS ACMI, INC 0.035" HYBRID WIRE, BOX OF 5 01/02/2019
GYRUS ACMI, INC 0.035" HYBRID WIRE, BOX OF 5 12/13/2018
LAKE REGION MANUFACTURING GUIDEWIRE,0.035 AMPLATZ,5-UP 11/07/2018
LAKE REGION MANUFACTURING GUIDEWIRE,0.035 AMPLATZ,5-UP 10/12/2018
GYRUS ACMI, INC 0.035" HYBRID WIRE, BOX OF 5 05/31/2018
GYRUS ACMI, INC 0.035" HYBRID WIRE, BOX OF 5 05/31/2018
GYRUS ACMI, INC 0.035" HYBRID WIRE, BOX OF 5 04/04/2018
-
-