20 results
·
39ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
FLEXI-SEAL CONTROL FMS KIT US
FDA Adverse Event
Malfunction
·CONVATEC INC.·Product code KNT·May 8, 2014
COULTER AC*T DIFF 2 ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code GKZ·May 7, 2012
DA VINCI XI
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL, INC·Product code NAY·May 26, 2026
SYNCHRON LX®20 PRO CLINICAL CHEMISTRY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JJE·July 22, 2011
4C PLUS COULTER CELL CONTROL
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JPK·September 30, 2011
GENETIC SYSTEMS RLAV EIA
FDA Adverse Event
Other
·BIO-RAD LABORATORIES·Product code LRM·April 24, 2006
DAVINCI XI
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL, INC·Product code NAY·April 11, 2026
DAVINCI 5
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL, INC·Product code NAY·October 31, 2025
UNICEL ® DXC600I SYNCHRON ® ACCESS ® CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·December 5, 2011
UNICEL ® DXC600I SYNCHRON ® ACCESS ® CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·December 5, 2011
UNICEL ® DXC600I SYNCHRON ® ACCESS ® CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·December 5, 2011
UNICEL® DXC 600I SYNCHRON® ACCESS® CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JJE·November 22, 2011
UNICEL® DXC 600I SYNCHRON® ACCESS® CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JJE·November 22, 2011
ZENITH FLEX AAA ENDOVASCULAR GRAFT ILIAC LEG
FDA Adverse Event
Injury
·COOK INC·Product code MIH·August 19, 2009
DAVINCI XI
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL, INC·Product code NAY·November 23, 2022
TREO ABDOMINAL STENT-GRAFT SYSTEM
FDA Adverse Event
Malfunction
·BOLTON MEDICAL, INC.·Product code MIH·August 6, 2024
TREO ABDOMINAL STENT-GRAFT SYSTEM
FDA Adverse Event
Malfunction
·BOLTON MEDICAL, INC.·Product code MIH·August 6, 2024
COULTER AC T 5DIFF CONTROL PLUS
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JPK·September 23, 2011
TREO ABDOMINAL STENT-GRAFT SYSTEM
FDA Adverse Event
Malfunction
·BOLTON MEDICAL, INC.·Product code MIH·August 6, 2024
BIOSITE
FDA Adverse Event
Other
·BIOSITE, INC.·Product code MGX·June 2, 2005