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
 

 
 
 1 
 2 
 3 
 4 
 > 
 
39 records meeting your search criteria returned- Product Code: BTR Patient Problem: Airway Obstruction Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MMJ SA DE CV (USD) SHILEY 01/17/2024
TELEFLEX MEDICAL SDN. BHD. FLEXI-SET UNCUFFED 3.5MM 08/31/2023
TELEFLEX MEDICAL LMA FASTRACH ETT, SU, SIZE 8.0 07/21/2023
MMJ SA DE CV (USD) SHILEY 06/30/2023
COVIDIEN SHILEY ET TUBE 06/06/2023
TELEFLEX MEDICAL ET TUBE, CUFFED, SPIRAL-FLEX 7.0 05/30/2023
SMITHS MEDICAL INTERNATIONAL, LTD. PORTEX BLUE LINE ULTRA CUFFED TUBE 02/24/2023
SMITHS MEDICAL INTERNATIONAL, LTD. PORTEX BLUE LINE ULTRA CUFFED TUBE 02/23/2023
SMITHS MEDICAL INTERNATIONAL, LTD. PORTEX ENDOTRACHEAL TUBE 02/20/2023
SMITHS MEDICAL INTERNATIONAL, LTD. INTUBATION PORTEX ENDOTRACHEAL TUBE 01/19/2023
-
-