5 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
DUROM ACETABULAR COMPONENT 54/48, CODE N
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·March 6, 2019
PULSE GEN MODEL 102
FDA Adverse Event
Injury
·CYBERONICS, INC·Product code LYJ·December 4, 2008
COULTER® LH 780 HEMATOLOGY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code GKZ·September 16, 2011
GYNECARE MORCELLEX TISSUE MORCELLATOR
FDA Adverse Event
Malfunction
·ETHICON INC.·Product code HET·July 29, 2013
ECHELON ENDO LINEAR CUTTERS
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·November 9, 2015