• 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 
 6 
 > 
 
59 records meeting your search criteria returned- Product Code: MNS Product Problem: Nonstandard Device Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
PHILIPS / RESPRONICS, INC. PHILIPS SYSTEM ONE 01/20/2023
PHILIPS/ RESPIRONICS INC. DREAMST AUTOSV H/C, DS 01/06/2023
RESPIRONICS, INC SYSTEM ONE REMSTAR AUTO A-FLEX 11/30/2022
RESPIRONICS, INC SYSTEM ONE REMSTAR AUTO A-FLEX 11/30/2022
RESPIRONICS, INC SYSTEM ONE REMSTAR AUTO A-FLEX 11/30/2022
RESPIRONICS, INC SYSTEM ONE REMSTAR AUTO A-FLEX 11/30/2022
RESPIRONICS, INC SYSTEM ONE REMSTAR AUTO A-FLEX 11/30/2022
PHILIPS/RESPIRONICS, INC. SYSTEM ONE 60 SERIES 10/24/2022
PHILIPS RESPIRONICS / RESPIRONICS INC. CPAP SYSTEM ONE 10/17/2022
PHILIPS /RESPIRONICS, INC. FACE MASK FOR BIPAP MACHINE 10/04/2022
-
-