40 results
·
74ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Other
×
SYSTEM 83 PLUS
FDA Adverse Event
Other
·CUSTOM ULTRASONICS·Product code KOG·November 20, 2012
CUSTOM ULTRASONICS, INC.
FDA Adverse Event
Other
·CUSTOM ULTRASONICS INC.·Product code FLG·September 18, 2008
CUSTOM ULTRASONICS
FDA Adverse Event
Other
·CUSTOM ULTRASONICS, INC.·Product code FLG·January 13, 2009
CUSTOM ULTRASONICS
FDA Adverse Event
Other
·CUSTOM ULTRASONICS, INC.·Product code FLG·December 6, 2010
SYSTEM 83 PLUS 2
FDA Adverse Event
Other
·CUSTOM ULTRASONICS INC.·Product code FEB·June 28, 2013
SYSTEM 83 PLUS 2
FDA Adverse Event
Other
·CUSTOM ULTRASONICS INC·Product code FEB·June 28, 2013
CUSTOM ULTRASONICS
FDA Adverse Event
Other
·CUSTOM ULTRASONICS, INC.·Product code FLG·August 1, 2011
CUSTOM ULTRASONICS SYSTEM 83 PLUS
FDA Adverse Event
Other
·CUSTOM ULTRASONICS INC.·Product code FLG·December 30, 2005
CUSTOM ULTRASONICS SYSTEMS 83 PLUS
FDA Adverse Event
Other
·CUSTOM ULTRASONICS, INC·Product code FLG·December 30, 2005
SYSTEM 83 PLUS
FDA Adverse Event
Other
·CUSTOM ULTRASONICS, INC.·Product code FLG·February 28, 2011
CUSTOM ULTRASONICS 83PLUS
FDA Adverse Event
Other
·CUSTOM ULTRASONICS INC·Product code FLG·December 20, 2006
CUSTOM ULTRASONICS
FDA Adverse Event
Other
·CUSTOM ULTRASONICS, INC.·Product code FLG·April 12, 2011
SYSTEM 83 PLUS WASHER/DISINFECTOR
FDA Adverse Event
Other
·CUSTOM ULTRASONICS, INC·Product code FLG·October 11, 2011
CUSTOM ULTRASONICS
FDA Adverse Event
Other
·CUSTOM ULTRASONICS, INC.·Product code FLG·January 26, 2009
CUSTOM ULTRASONICS
FDA Adverse Event
Other
·CUSTOM ULTRASONICS INC·Product code NVE·February 19, 2009
CUSTOM ULTRASONIC
FDA Adverse Event
Other
·CUSTOM ULTRASONICS INC·Product code NVE·February 19, 2009
CUSTOM ULTRASONICS
FDA Adverse Event
Other
·CUSTOM ULTRASONICS INC.·Product code FLG·August 27, 2012
CUSTOM ULTRASONICS
FDA Adverse Event
Other
·CUSTOM ULTRASONICS, INC.·Product code FLG·January 15, 2009
SYSTEM 83 PLUS 2
FDA Adverse Event
Other
·CUSTOMER ULTRASONICS, INC.·Product code FEB·June 28, 2013
SYNCHRON LXI 725 CLINICAL SYSTEM
FDA Adverse Event
Other
·BECKMAN COULTER, INC.·Product code MMI·October 6, 2008