40 results · 74ms · Sources: EU EUDAMED, US FDA

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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