3 results
·
26ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
CAIMAN DISP.INSTR.NON ARTICUL. D:5/360MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code GEI·March 12, 2014
ACCESS
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - AIBONITO·Product code FRN·November 26, 2012
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·September 23, 2010