• 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
 

 
 < 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 > 
 
115 records meeting your search criteria returned- Product Code: DYB Product Problem: Device Operates Differently Than Expected Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ST. JUDE MEDICAL, INC. (AF-MINNETONKA) SWARTZ¿ BRAIDED TRANSSEPTAL GUIDING INTR 10/23/2014
ST. JUDE MEDICAL, INC. (AF-MINNETONKA) AGILIS¿ NXT STEERABLE INTRODUCER DUAL-RE 10/23/2014
GALT MEDICAL CORP GALT STIFFEN MIRCO-INTRODUCER KIT 10/08/2014
B. BRAUN MEDICAL, INC. INTROCAN SAFETY IV CATHETER 09/29/2014
BIOSENSE WEBSTER, INC (IRWINDALE) PREFACE® GUIDING SHEATH WITH MULTIPURPOS 09/25/2014
GREATBATCH MEDICAL MOBICATH STEERABLE SHEATH 09/17/2014
ARSTASIS INC. AXERA 2 ACCESS SYTEM 09/17/2014
W.L. GORE & ASSOCIATES GORE® DRYSEAL SHEATH 09/03/2014
W.L. GORE & ASSOCIATES GORE® DRYSEAL SHEATH 06/24/2014
VASCULAR SOLUTIONS, INC. MICRO-INTRODUCER KIT 06/19/2014
-
-