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
 

 
 
 1 
 2 
 > 
 
14 records meeting your search criteria returned- Product Code: FNL Product Problem: Human Factors Issue Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ARJOHUNTLEIGH POLSKA SP Z O. O. MINUET 2 06/12/2018
ARJOHUNTLEIGH POLSKA SP Z O.O. ENTERPRISE 8000 04/26/2018
ARJOHUNTLEIGH POLSKA CITADEL PLUS 03/29/2018
ARJOHUNTLEIGH POLSKA CITADEL PLUS 03/27/2018
ARJOHUNTLEIGH POLSKA CITADEL PLUS 03/09/2018
ARJOHUNTLEIGH POLSKA CITADEL PLUS 02/26/2018
ARJOHUNTLEIGH POLSKA ENTERPRISE 9000X 02/07/2018
ARJOHUNTLEIGH POLSKA CITADEL PATIENT CARE SYSTEM 01/09/2018
ARJOHUNTLEIGH POLSKA CITADEL PLUS 10/30/2017
ARJOHUNTLEIGH POLSKA ENTERPRISE 5000 10/05/2017
-
-