• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

  • 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 
 > 
 
72 records meeting your search criteria returned- Product Code: BSZ Product Problem: Intermittent Communication Failure Report Date From: 01/1/2017
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DRÄGERWERK AG & CO. KGAA PERSEUS 09/29/2022
DRÄGERWERK AG & CO. KGAA APOLLO 08/30/2022
DRÄGERWERK AG & CO. KGAA PERSEUS A500 08/24/2022
DRÄGERWERK AG & CO. KGAA PRIMUS 08/18/2022
DRÄGERWERK AG & CO. KGAA PRIMUS 07/18/2022
DRÄGERWERK AG & CO. KGAA APOLLO 07/18/2022
DRÄGERWERK AG & CO. KGAA PRIMUS 07/06/2022
DRÄGERWERK AG & CO. KGAA APOLLO 03/11/2022
DRÄGERWERK AG & CO. KGAA PRIMUS 02/25/2022
DRÄGERWERK AG & CO. KGAA PERSEUS A500 02/02/2022
-
-