• 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
 

 
 < 
 1 
 2 
 3 
 4 
 5 
 > 
 
48 records meeting your search criteria returned- Product Code: LHI Product Problem: Crack Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITHS MEDICAL ASD, INC. CASSETTE LEGACY 01/30/2023
SMITHS MEDICAL ASD, INC. CASSETTE LEGACY 01/30/2023
SMITHS MEDICAL ASD, INC. CASSETTE LEGACY 01/30/2023
SMITHS MEDICAL ASD, INC. CASSETTE LEGACY 01/30/2023
NULL MEDEX BIFURCATED FLUID ADMINISTRATION SE 05/11/2022
SMITHS MEDICAL ASD, INC. NRFIT 01/26/2022
BECTON DICKINSON BD SMARTSITE¿ VENTED VIAL ACCESS DEVICE, 01/25/2022
SMITHS MEDICAL ASD, INC. CASSETTE MEDI RESERVOIR 10/25/2021
SMITHS MEDICAL ASD, INC. CASSETTE MEDI RESERVOIR 10/25/2021
SMITHS MEDICAL ASD, INC. CASSETTE MEDI RESERVOIR 10/25/2021
-
-