3 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 13, 2014
SOLETRA
FDA Adverse Event
Injury
·MEDTRONIC EUROPE SARL·Product code MHY·October 12, 2010
IMMERSION HYDROBATH
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ILJ·December 12, 2012