3 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
TOTAL ASR FEM IMP SIZE 49
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·June 4, 2014
ELIMINATOR ICW
FDA Adverse Event
Malfunction
·ARTHROCARE CORPORATION·Product code GEI·November 21, 2012
PUMP MMT-522NAS PRDGM INS V2.2 SK EN
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·September 22, 2010