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
 

 
 
7 records meeting your search criteria returned- Product Code: LRO Product Problem: Patient-Device Incompatibility Report Date From: 01/1/2018
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SC003 SC-FORT MILL SHOULDER PACK (SHWCZ)683 12/23/2019
BECTON, DICKINSON AND COMPANY CHLORAPEP IN PICC LINE DRSG CHNG W/ BIOP 07/30/2019
MEX03 MEXICO-JUAREZ PRESOURCE HERNIA PACK (HPSPD)568 06/19/2019
MEX03 MEXICO-JUAREZ PRESOURCE BMOB PHACO PACK (PHKOA)888 04/26/2019
ALCON RESEARCH, LLC - HOUSTON CUSTOM-PAK SURGICAL PROCEDURE PACK 03/15/2019
MEX03 MEXICO-JUAREZ PRESOURCE CATARACT PACK (CPHGH)867 11/02/2018
ALCON RESEARCH, LTD. - HOUSTON CUSTOM-PAK SURGICAL PROCEDURE PACK 10/10/2018
-
-