3 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
NA
FDA Adverse Event
Injury
·STERILMED, INC.·Product code NUJ·June 10, 2014
FULL ELECTRIC FOOT SPRING 9153638201
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code FNL·July 1, 2015
KENTROX SL-S 65/16 STEROID
FDA Adverse Event
Malfunction
·BIOTRONIK SE & CO. KG·Product code LWS·November 16, 2012