• 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 
 > 
 
47 records meeting your search criteria returned- Product Code: MWI Product Problem: Device Alarm System Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
INVIVO CORPORATION XPER FLEX CARDIO PHYSIOMONITORING SYSTEM 03/20/2020
INVIVO CORPORATION XPER FLEX CARDIO PHYSIOMONITORING SYSTEM 03/19/2020
INVIVO CORPORATION XPER FLEX CARDIO PHYSIOMONITORING SYSTEM 03/19/2020
INVIVO CORPORATION XPER FLEX CARDIO PHYSIOMONITORING SYSTEM 03/19/2020
MASIMO - 52 DISCOVERY KIT, RAD-97 PULSE CO-OXIMETER 08/22/2019
INVIVO CORPORATION XPER FLEX CARDIO PHYSIOMONITORING SYSTEM 07/21/2019
WELCH ALLYN, INC. CONNEX 06/27/2019
MASIMO - 40 PARKER KIT, RAD-97 PULSE CO-OXIMETER 04/05/2019
INVIVO CORPORATION XPER FLEX CARDIO PHYSIOMONITORING SYSTEM 02/13/2019
MASIMO CORPORATION ROOT 10/04/2018
-
-