3 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
HEARTSTART ONSITE
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·February 18, 2014
ACCU-CHEK AVIVA TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·October 25, 2007
PENUMBRA SYSTEM REPERFUSION CATHETER 041
FDA Adverse Event
Injury
·PENUMBRA, INC.·Product code NRY·October 3, 2012