3 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
PENUMBRA SYSTEM REPERFUSION CATHETER 041
FDA Adverse Event
Injury
·PENUMBRA, INC.·Product code NRY·October 3, 2012
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC, USA·Product code LFR·June 12, 2007
THERAKOS CELLEX PHOTOPHERESIS SYSTEM
FDA Adverse Event
Malfunction
·THERAKOS, INC.·Product code LNR·February 18, 2014