3 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
TOTAL ASR FEM IMP SIZE 53
FDA Adverse Event
Malfunction
·DEPUY INTL., LTD. - 8010379·Product code KWA·November 17, 2010
OT ULTRAMINI METER
FDA Adverse Event
Injury
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 5, 2014
TRANSTAR STRETCHER
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FPO·December 7, 2012