3 results
·
16ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 30, 2014
PENUMBRA SYSTEM REPERFUSION CATHETER 054
FDA Adverse Event
Malfunction
·PENUMBRA, INC.·Product code NRY·June 28, 2012
PROXIMATE*ILS CURVED CIR STAPL
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·September 21, 2010