• 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
 

 
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 > 
 
55 records meeting your search criteria returned- Product Code: FOZ Patient Problem: Skin Inflammation/ Irritation Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
C.R. BARD, INC. (BASD) -3006260740 BARD POWERGLIDE PRO 05/03/2023
BD (SUZHOU) BD INTIMA-II IV CATHETER 04/24/2023
BECTON DICKINSON INFUSION THERAPY SYSTEM BD INSYTE¿ AUTOGUARD¿ BC SHIELDED IV CAT 03/29/2023
BD (SUZHOU) BD PEGASUS¿ SAFETY CLOSED IV CATHETER SY 03/20/2023
ARROW INTERNATIONAL LLC ARROW EXT DWELL CATH DEVICE 22GAX6CM 02/03/2023
BECTON DICKINSON MEDICAL (SINGAPORE) BD INSYTE¿ IV WINGED CATHETER 01/24/2023
BD (SUZHOU) BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM 01/05/2023
SMITHS MEDICAL ASD, INC. JELCO SERIVA IV CATHETER 10/07/2022
SMITHS MEDICAL ASD, INC. JELCO SERIVA IV CATHETER 10/06/2022
TERUMO PHILIPPINES CORPORATION TERUMO SURFLO INTRAVENOUS CATHETER 09/16/2022
-
-