• 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 
 
 
49 records meeting your search criteria returned- Product Code: FJS Patient Problem: Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
UNKNOWN PD CATHETER 08/09/2023
COVIDIEN MFG SOLUTIONS S.A. ARGYLE 07/26/2023
Unknown Manufacturer PD CATHETER 07/06/2023
COVIDIEN MFG SOLUTIONS S.A. PERITONEAL CATHETER 10/18/2022
COVIDIEN MFG SOLUTIONS S.A. DIALYSIS UNKNOWN 07/15/2022
COVIDIEN MFG SOLUTIONS S.A. PERITONEAL CATHETER 06/27/2022
COVIDIEN MFG SOLUTIONS S.A. PERITONEAL CATHETER 03/29/2022
COVIDIEN MFG SOLUTIONS S.A. PERITONEAL CATHETER 09/02/2021
COVIDIEN MFG SOLUTIONS S.A. ARGYLE 04/20/2021
-
-