3 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
7900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·April 15, 2014
VITROS 3600 IMMUNODIAGNOSTIC SYSTEM
FDA Adverse Event
Malfunction
·ORTHO-CLINICAL DIAGNOSTICS·Product code KHO·October 7, 2010
GII STANDARD TIBIA B
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code JWH·December 6, 2012