• 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 
 > 
 
15 records meeting your search criteria returned- Product Code: BTR Patient Problem: Respiratory Failure Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MMJ SA DE CV (USD) UNSPECIFIED ENDOTRACH TUBE 07/07/2023
SMITHS MEDICAL INTERNATIONAL, LTD. PORTEX BLUE LINE ULTRA CUFFED TUBE 02/23/2023
MALLINCKRODT MEDICAL SHILEY 01/05/2023
MMJ SA DE CV (USD) SHILEY 10/10/2022
SMITHS MEDICAL INTERNATIONAL, LTD. PORTEX ENDOTRACHEAL TUBE W/HOLDER AND CO 08/16/2022
MMJ SA DE CV (USD) SHILEY 04/12/2022
ST PAUL PORTEX TRACHEOSTOMY TUBE 03/10/2022
MMJ SA DE CV (USD) SHILEY 09/02/2021
SMITHS MEDICAL INTERNATIONAL, LTD. PORTEX ENDOTRACHEAL TUBES SACETT 07/14/2021
SMITHS MEDICAL INTERNATIONAL, LTD. PORTEX ENDOTRACHEAL TUBES SACETT 07/13/2021
-
-