33 results
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36ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Other
×
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