• 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 
 > 
 
18 records meeting your search criteria returned- Product Code: DRX Patient Problem: Skin Irritation Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
LEONHARD LANG GMBH SKINTACT 09/30/2020
COVIDIEN ELECTRODE H49P SOLID GEL 09/28/2020
LEONHARD LANG GMBH SKINTACT 08/20/2020
D.O. WEAVER AND COMPANY NUPREP SKIN PREP GEL 07/30/2020
GRAPHIC CONTROLS DBA NISSHA MEDICAL TECH PRIMARY CARE BY MDP ECG MONITORING ELECT 05/28/2020
LEONHARD LANG GMBH WHITESENSOR 04/20/2020
LEONHARD LANG GMBH SKINTACT 04/15/2020
LEONHARD LANG GMBH SKINTACT 03/24/2020
LEONHARD LANG GMBH SKINTACT 01/09/2020
LEONHARD LANG GMBH SKINTACT 12/05/2019
-
-