3 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
TELIGEN
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·February 5, 2013
WIRELESS FOOTSWITCH
FDA Adverse Event
Malfunction
·SIEMENS MEDICAL SOLUTIONS USA, INC.·Product code JAA·December 19, 2010
AMS SPECTRA CONCEALABLE PENILE PROSTHESIS
FDA Adverse Event
Injury
·AMERICAN MEDICAL SYSTEMS (MN)·Product code FAE·July 18, 2014