3 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
ASR UNI FEMORAL IMPL SIZE 49
FDA Adverse Event
Injury
·DEPUY INTL., LTD - 8010379·Product code KWA·June 5, 2014
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·November 13, 2012
ULTRAPULSE ENCORE AESTHETIC PACKAGE
FDA Adverse Event
Injury
·LUMENIS LTD. YOKNEAM,·Product code GEX·September 30, 2010