• 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
 

 
 < 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 > 
 
165 records meeting your search criteria returned- Product Code: HIF 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
W.O.M WORLD OF MEDICINE GMBH AIRSEAL IFS, 110V 04/12/2021
W.O.M WORLD OF MEDICINE GMBH AIRSEAL IFS, 110V 04/08/2021
W.O.M WORLD OF MEDICINE GMBH AIRSEAL IFS UNIT 110V 03/23/2021
W.O.M. WORLD OF MEDICINE GMBH AIRSEAL IFS, 110V 03/15/2021
CONSOLIDATED MEDICAL EQUIPMENT AIRSEAL 5/120MM PORT 03/05/2021
CONSOLIDATED MEDICAL EQUIPMENT AIRSEAL 12/100MM LPI PORT 03/02/2021
CONSOLIDATED MEDICAL EQUIPMENT TRILUMEN FILTERED TUBE SET 03/01/2021
W.O.M. WORLD OF MEDICINE GMBH AIRSEAL IFS, 110V 02/25/2021
OLYMPUS MEDICAL SYSTEMS CORP. ENDOSCOPIC CO2 REGULATION UNIT 02/02/2021
STRYKER ENDOSCOPY-SAN JOSE PKG, 40L CORE SIDNE READY INSUFFLATOR 01/13/2021
-
-