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·May 31, 2014
WAVELIGHT EX500 ECIMER LASER
FDA Adverse Event
Injury
·WAVELIGHT GMBH·Product code LZS·November 14, 2012
MINI-CAP, DISCONNECT W/PVP-1SOLUTION
FDA Adverse Event
Death
·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·September 23, 2010