3 results
·
14ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
CAIMAN DISP. INSTR. NON ARTICUL. D:5/360MM
FDA Adverse Event
Malfunction
·AESCULAP AG AND CO. KG·Product code GEI·December 12, 2014
BARD
FDA Adverse Event
Malfunction
·BARD·Product code LJT·May 8, 2014
FREESTYLE
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC, USA·Product code NBW·October 24, 2007