64 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Other
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BOWEL GRASPER INSTRUMENT
FDA Adverse Event
Other
·INTUITIVE SURGICAL,INC.·Product code NAY·May 31, 2013
BOWEL GRASPER INSTRUMENT
FDA Adverse Event
Other
·INTUITIVE SURGICAL,INC.·Product code NAY·May 31, 2013
LAPROSCOPIC BOWEL GRASPER
FDA Adverse Event
Other
·KARL STORZ ENDOSCOPY - AMERICA, INC.·Product code GCJ·May 11, 2016
ZASSI BOWEL MANAGEMENT SYSTEM
FDA Adverse Event
Other
·HOLLISTER INCORPORATED·Product code KNT·May 14, 2009
ZASSI BOWEL MANAGEMENT SYSTEM
FDA Adverse Event
Other
·HOLLISTER INCORPORATED·Product code KNT·September 27, 2007
ZASSI BOWEL MANAGEMENT SYSTEM
FDA Adverse Event
Other
·HOLLISTER INCORPORATED·Product code KNT·September 27, 2007
ACTIFLO INDWELLING BOWEL CATHETER SYSTEM
FDA Adverse Event
Other
·HOLLISTER, INC.·Product code KNT·February 18, 2010
ACTIFLO INDWELLING BOWEL CATHETER SYSTEM
FDA Adverse Event
Other
·HOLLISTER, INC.·Product code KNT·November 25, 2009
ACTIFLO INDWELLING BOWEL CATHETER SYSTEM
FDA Adverse Event
Other
·HOLLISTER, INC.·Product code MIP·October 14, 2010
ACTIFLO INDWELLING BOWEL CATHETER SYSTEM
FDA Adverse Event
Other
·HOLLISTER, INC.·Product code KNT·September 29, 2011
ACTIFLO INDWELLING BOWEL CATHETER SYSTEM
FDA Adverse Event
Other
·HOLLISTER, INC.·Product code KNT·May 19, 2011
ACTIFLO INDWELLING BOWEL CATHETER SYSTEM
FDA Adverse Event
Other
·HOLLISTER, INC.·Product code MIP·July 22, 2010
ACTIFLO INDWELLING BOWEL CATHETER SYSTEM
FDA Adverse Event
Other
·HOLLISTER, INC.·Product code KNT·July 22, 2010
KERAMOS HIP
FDA Adverse Event
Other
·ENCORE MEDICAL, L.P.·Product code LPH·December 22, 2010
SHELHIGH PERICARDIAL PATCH
FDA Adverse Event
Other
·SHELHIGH, INC.·Product code MFX·July 12, 2000
DEROYAL
FDA Adverse Event
Other
·G.A. SURGICAL (PVT) LTD.·Product code HFX·December 6, 2013
ORTHO SUMMIT TM SAMPLE HANDLING SYSTEM
FDA Adverse Event
Other
·HAMILTON BONADUZ AG·Product code JTC·September 15, 1997
ORTHO SUMMIT TM SAMPLE HANDLING SYSTEM
FDA Adverse Event
Other
·HAMILTON BONADUZ AG·Product code JTC·September 15, 1997
PULSE GEN MODEL 102
FDA Adverse Event
Other
·CYBERONICS, INC.·Product code LYJ·March 23, 2007
PULSE GEN MODEL 102
FDA Adverse Event
Other
·CYBERONICS, INC.·Product code LYJ·December 7, 2006