4 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
URIC ACID REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code KNK·April 15, 2011
G400 GENERATOR, GYRUS
FDA Adverse Event
Malfunction
·GYRUS MEDICAL, LTD.·Product code GEI·October 20, 2010
CARE ASSIST BED
FDA Adverse Event
Malfunction
·HILL-ROM PLUVIGNER·Product code FNL·February 20, 2014
6.5CM ADULT CRANI ATTACHMT
FDA Adverse Event
Malfunction
·THE ANSPACH EFFORT, INC.·Product code HBE·December 18, 2012