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 
 > 
 
12 records meeting your search criteria returned- Product Code: FRN Patient Problem: Respiratory Failure Report Date From: 01/1/2018
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BD / CAREFUSION 303, INC. BD ALARIS INFUSION PUMP AND MODULE 12/29/2022
BD / CAREFUSION 303, INC. BD ALARIS INFUSION PUMP AND MODULE 12/29/2022
ICU MEDICAL, INC. PLUM 360 10/31/2022
CAREFUSION SD ALARIS SYSTEM 08/10/2021
CAREFUSION SD ALARIS SYSTEM 08/10/2021
CAREFUSION 303, INC. ALARIS 04/27/2021
CAREFUSION SD ALARIS PUMP MODULE 04/19/2021
NULL PUMP, INFUSION 03/10/2021
ICU MEDICAL COSTA RICA LTD. BOMBA DE INFUSION PLUM 360 COMPATIBLE CO 08/18/2020
CAREFUSION ALARIS PUMP MODULE 07/30/2019
-
-