8 results
·
25ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 14, 2013
TAXUS LIBERTE PACLITAXEL-ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·August 12, 2014
DAMON COPPER NITI WIRE
FDA Adverse Event
Malfunction
·ORMCO CORP.·Product code DZC·February 28, 2008
5.0 CM SHORT ATTACHMENT
FDA Adverse Event
Malfunction
·DEPUY SYNTHES PRODUCTS LLC·Product code HBC·January 18, 2019
5.0CM SHORT ATTACHMENT
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HBC·June 29, 2017
PENUMBRA SMART COIL
FDA Adverse Event
Injury
·PENUMBRA, INC.·Product code HCG·February 3, 2017
5.0 CM SHORT ATTACHMENT
FDA Adverse Event
Malfunction
·DEPUY SYNTHES PRODUCTS LLC·Product code HBC·January 11, 2019
11.0 CM LONG ATTACHMENT
FDA Adverse Event
Malfunction
·DEPUY SYNTHES PRODUCTS LLC·Product code HBC·April 2, 2018