6,620 results
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33ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MOSAIQ
FDA Adverse Event
Malfunction
·IMPAC MEDICAL SYSTEMS, INC.·Product code IYE·March 4, 2015
COROMETRICS
FDA Adverse Event
COROMETRICS MED SYSTEMS·Product code DRX·June 30, 1998
ANGIOJET DVX RHEOLYTIC THROMBECTOMY CATHETER
FDA Adverse Event
Injury
·POSSIS MEDICAL, INC.·Product code DXE·October 28, 2005
SIPHONGUARD, CSF FLD CONTRL DV
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC.·Product code JXG·April 6, 2010
SIPHONGUARD, CSF FLD CONTRL DV
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC.·Product code JXG·May 18, 2010
SIPHONGUARD, CSF FLD CONTRL DEVICE
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC./MEDOS S.A.·Product code JXG·October 17, 2008
SIPHONGUARD, OSF FLD CONTROL DV
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC/MEDOS S.A.·Product code JXG·June 10, 2009
SIPHONGUARD, CSF FLD CONTROL DEVICE
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC./ MEDOS S.A.·Product code JXG·June 10, 2008
SIPHONGUARD, CSF FLD CONTRL DV
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC./MEDOS S.A.·Product code JXG·March 31, 2009
SIPHONGUARD, CSF FLD CONTROL DV
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC/MEDOS S.A.·Product code JXG·March 25, 2009
SIPHONGUARD, CSF FLD CONTROL DEVICE
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC/MEDOS S.A.·Product code JXG·July 6, 2006
SIPHONGUARD, CSF FLD CONTROL DEVICE
FDA Adverse Event
Injury
·CODMAN & SHURTLEFF, INC./ MEDOS S.A.·Product code JXG·March 18, 2008
SIPHONGUARD, CSF FLD CONTRL DV
FDA Adverse Event
Injury
·INTEGRA LIFESCIENCES MANSFIELD·Product code JXG·November 20, 2019
VIASYS
FDA Adverse Event
Malfunction
·CAREFUSION·Product code CBK·August 30, 2011
CHAIR, SHOWER ,WITH BACK,FLD, 300 LB
FDA Adverse Event
Injury
·MEDLINE INDUSTRIES, LP·Product code ILS·September 10, 2025
COMMODE,3-IN-1,STEEL,FLD,350 LB
FDA Adverse Event
Injury
·MEDLINE INDUSTRIES, LP·Product code ILS·February 5, 2025
COMMODE,3-IN-1,STEEL,FLD,350 LB
FDA Adverse Event
Injury
·MEDLINE INDUSTRIES, LP·Product code ILS·February 4, 2025
SMARTSITE 20MM VENTED VIAL ACCESS DEVICE
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FPA·May 10, 2021
CONSTELLATION VISION SYSTEM
FDA Adverse Event
Malfunction
·ALCON RESEARCH, LLC - IRVINE TECHNOLOGY CENTER·Product code HQC·November 26, 2024
CAREFUSION
FDA Adverse Event
Malfunction
·CAREFUSION·Product code CBK·June 12, 2015