8 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VACUETTE BLOOD COLLECTION TUBE 3ML K2E K2EDTA
FDA Adverse Event
Malfunction
·GREINER BIO-ONE NA INC.·Product code JKA·November 2, 2020
CROSSEAL APPLICATION DEVICE
FDA 510(k)
FDA Class 2
·General Hospital
LIFETEC ELITE V1.0
FDA Adverse Event
Malfunction
·IT SYNERGISTICS, LLC·Product code MMH·July 29, 2016
ORTHO PROVUE ANALYZER
FDA Adverse Event
Malfunction
·MICRO TYPING SYSTEMS, INC.·Product code KSZ·November 21, 2006
ORTHO PROVUE ANALYZER
FDA Adverse Event
Malfunction
·MICRO TYPING SYSTEMS, INC.·Product code KSZ·November 22, 2006
ORTHO PROVUE ANALYZER
FDA Adverse Event
Malfunction
·MICRO TYPING SYSTEMS, INC.·Product code KSZ·November 22, 2006
ORTHO PROVUE ANALYZER
FDA Adverse Event
Malfunction
·MICRO TYPING SYSTEMS, INC.·Product code KSZ·November 22, 2006
ORHTO PROVUE ANALYZER
FDA Adverse Event
Malfunction
·MICRO TYPING SYSTEMS, INC.·Product code KSZ·November 22, 2006