3 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETER
FDA Adverse Event
Malfunction
·CORDIS DE MEXICO·Product code LIT·June 19, 2014
BUBBLE DETECTOR CABLE - ADULT
FDA Adverse Event
Injury
·MEDTRONIC PERFUSION SYSTEMS·Product code DWA·October 18, 2010
VITROS 5600 INTEGRATED SYSTEM
FDA Adverse Event
Malfunction
·ORTHO-CLINICAL DIAGNOSTICS·Product code JJE·December 21, 2012