• 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 
 > 
 
33 records meeting your search criteria returned- Product Code: BZD Product Problem: Detachment of Device or Device Component Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
RESPIRONICS INC. DREAMSTATION CPAP 05/12/2022
RESPIRONICS, INC. S PERFORMAX SU DOM WITH EE LEAK 2 01/07/2022
PHILIPS / RESPIRONICS, INC. CPAP DREAMSTATION 11/10/2021
PHILIPS / RESPIRONICS, INC. CPAP DREAMSTATION 11/10/2021
RESPIRONICS, INC. AF541 EE LEAK 1 FULL FACE MASK 11/09/2021
PHILIPS / RESPIRONICS, INC. DREAMSTATION 11/03/2021
RESMED CORP. RESMED CPAP 08/23/2021
PHILIPS / RESPIRONICS, INC. DREAMSTATION AUTO CPAP HUMHT CELL 08/10/2021
RESPIRONICS INC DREAMWEAR UNDER THE NOSE MASK 12/10/2020
RESMED CORP. AIRSENSE 10 07/09/2020
-
-