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

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 
 7 
 8 
 9 
 10 
 > 
 
443 records meeting your search criteria returned- Product Code: BSZ Product Problem: Pressure Problem Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DRÄGERWERK AG & CO. KGAA FABIUS GS 12/01/2022
DRÄGERWERK AG & CO. KGAA FABIUS GSP 11/29/2022
DRÄGERWERK AG & CO. KGAA FABIUS GSP 11/29/2022
DRÄGERWERK AG & CO. KGAA FABIUS GS PREMIUM 09/28/2022
DRÄGERWERK AG & CO. KGAA FABIUS GS PREMIUM 09/07/2022
DRÄGERWERK AG & CO. KGAA FABIUS GS PREMIUM 08/30/2022
DRÄGERWERK AG & CO. KGAA FABIUS TIRO 07/14/2022
DRÄGERWERK AG & CO. KGAA FABIUS MRI 07/07/2022
DRÄGERWERK AG & CO. KGAA FABIUS GS 06/28/2022
DATEX-OHMEDA, INC. AESTIVA MRI 05/27/2022
-
-