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

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
 

 
 
8 records meeting your search criteria returned- Product Code: BSO Product Problem: Device Issue Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
EPIMED INTERNATIONAL INC 20G SPIROL 06/26/2018
EPIMED INTERNATIONAL INC 20G SPIROL CATHETER 05/02/2018
EPIMED INTERNATIONAL INC. SPIROL 04/23/2018
EPIMED INTERNATIONAL INC. TUN-L-XL 11/20/2017
EPIMED INTERNATIONAL INC. TUN-L-XL 11/20/2017
EPIMED INTERNATIONAL INC. VERSA-KATH 10/18/2017
EPIMED INTERNATIONAL INC. VERSA-KATH 10/02/2017
EPIMED INTERNATIONAL INC. TUN-L-XL 06/15/2017
-
-