• 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 
 
 
11 records meeting your search criteria returned- Product Code: BSZ Patient Problem: Cyanosis Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
DATEX-OHMEDA, INC. AISYS CS2 02/06/2024
GE HEALTHCARE TECHNOLOGIES, INC. / DATEX ANESTHESIA CART 01/03/2024
DRÄGERWERK AG & CO. KGAA PRIMUS INFINITY EMPOWERED 02/08/2022
DRÄGERWERK AG & CO. KGAA PRIMUS 10/29/2020
DRÄGERWERK AG & CO. KGAA APOLLO 05/14/2020
DRÄGERWERK AG & CO. KGAA FABIUS TIRO 06/12/2019
DATEX-OHMEDA, INC. AVANCE 05/10/2019
DRÄGERWERK AG & CO. KGAA PRIMUS 10/25/2018
DRÄGERWERK AG & CO. KGAA PERSEUS A500 10/15/2018
DRAEGER MEDICAL GMBH PRIMUS IE 04/01/2015
-
-