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
 

 
 < 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 16 
 > 
 
156 records meeting your search criteria returned- Product Code: FNM Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
GETINGE (SUZHOU) CO., LTD. AUTO LOGIC 05/24/2019
JOERNS HEALTHCARE DERMAFLOAT LAL SYSTEM 05/01/2019
JOERNS HEALTHCARE DERMAFLOAT LAL SYSTEM 05/01/2019
MEDLINE INDUSTRIES INC. UNKNOWN AIR MATTRESS 04/30/2019
JOERNS HEALTHCARE DERMAFLOAT LAL SYSTEM 04/15/2019
JOERNS HEALTHCARE DERMAFLOAT LAL SYSTEM 04/12/2019
JOERNS HEALTHCARE DOLPHIN FIS 03/29/2019
JOERNS HEALTHCARE P.R.O. MATT PLUS CONTROL UNIT 03/29/2019
GETINGE (SUZHOU) CO., LTD. NIMBUS 4 03/26/2019
JOERNS HEALTHCARE DERMAFLOAT LAL SYSTEM 03/25/2019
-
-