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
 

 
 < 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 > 
 
110 records meeting your search criteria returned- Product Code: BSZ Product Problem: Intermittent Communication Failure Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DRÄGERWERK AG & CO. KGAA PERSEUS A500 02/16/2021
DRÄGERWERK AG & CO. KGAA PERSEUS A500 02/08/2021
DRÄGERWERK AG & CO. KGAA APOLLO 12/17/2020
DRÄGERWERK AG & CO. KGAA PERSEUS A500 12/07/2020
DRÄGERWERK AG & CO. KGAA PERSEUS A500 11/30/2020
DRÄGERWERK AG & CO. KGAA PRIMUS 11/19/2020
DRÄGERWERK AG & CO. KGAA PERSEUS A500 11/06/2020
DRÄGERWERK AG & CO. KGAA PRIMUS 11/04/2020
DRÄGERWERK AG & CO. KGAA PERSEUS A500 10/30/2020
DRÄGERWERK AG & CO. KGAA PERSEUS A500 10/28/2020
-
-