33 results · 36ms · Sources: EU EUDAMED, US FDA

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ENTRIFLEX FEEING TUBES

FDA Adverse Event
Other ·COVIDIEN·Product code FPD·August 12, 2014

SORIN AF 620 W/LOOP 10

FDA Adverse Event
Other ·SORIN GROUP USA, INC.·Product code DWE·June 25, 2010

TRIPLER ARMY HONOLULU HI1

FDA Adverse Event
Other ·SORIN GROUP USA, INC.·Product code DWE·June 25, 2010

C20880 AD./ECMO PTS

FDA Adverse Event
Other ·SORIN GROUP ITALIA·Product code DWE·April 6, 2010

UNDETERMINED

FDA Adverse Event
Other ·UNDETERMINED·Product code FAE·September 13, 1996

PERF ALLIANCE OK CITY OK 1

FDA Adverse Event
Other ·SORIN GROUP USA, INC.·Product code DWE·May 11, 2012

MERCY HSP PITTSBURGH PA 1

FDA Adverse Event
Other ·SORIN GROUP USA, INC.·Product code DWE·April 13, 2012

MENTOR

FDA Adverse Event
Other ·MENTOR·Product code FAE·October 31, 2003

CUSTOMPAC

FDA Adverse Event
Other ·BAXTER HEALTHCARE CORP.·Product code DWE·August 30, 2000

PERFUSION PACK, PUMP & TABLE W/VANGUARD; ST. JOSEPH HOSPITAL

FDA Adverse Event
Other ·COBE CARDIOVASCULAR, INC.·Product code DWE·May 24, 2005

DEBORAH HEART & LUNG 6

FDA Adverse Event
Other ·COBE CARDIOVASCULAR, INC.·Product code DWE·June 7, 2005

UNKNOWN

FDA Adverse Event
Other ·AMERICAN MEDICAL SYSTEMS·Product code FAE·January 18, 1995

ULTREX

FDA Adverse Event
Other ·AMS·Product code FAE·January 19, 1995

RUBY MEM MORGANTOWN,WV1

FDA Adverse Event
Other ·SORIN GROUP USA, INC.·Product code DWE·January 30, 2007

DURA II PENILE IMPLANT

FDA Adverse Event
Other ·UROHEALTH SYSTEMS, INC.·Product code FAE·April 4, 1997

SPECTRA CONCEALABLE PENILE PROSTHESIS

FDA Adverse Event
Other ·AMERICAN MEDICAL SYSTEMS, INC.·Product code FAE·March 28, 2011

MALLEABLE PENILE IMPLANT

FDA Adverse Event
Other ·AMERICAN MEDICAL SYSTEMS, INC.·Product code FAE·December 23, 1995

HEMOCONCENTRATOR PACK

FDA Adverse Event
Other ·COBE CARDIOVASCULAR, INC.·Product code DWE·January 28, 2000

PERFUSION PACK, ECMO PACK, BAXTER PERFUSION SERVICES, AKRON

FDA Adverse Event
Other ·COBE CARDIOVASCULAR, INC.·Product code DWE·May 22, 2003

PERFUSION PACK, OPTIMA XP 4000 VVR, FMC/PRESBYTERIAN, PHILAD

FDA Adverse Event
Other ·COBE CARDIOVASCULAR, INC.·Product code DWE·May 15, 2003