64 results · 23ms · Sources: EU EUDAMED, US FDA

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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