17 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
PROSTHESIS, INTERVERTEBRAL DISC
FDA Adverse Event
Injury
·SYNTHES USA·Product code MJO·October 26, 2016
PROSTHESIS, INTERVERTEBRAL DISC
FDA Adverse Event
Injury
·SYNTHES USA·Product code MJO·October 26, 2016
PROSTHESIS, INTERVERTEBRAL DISC
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code MJO·October 26, 2016
PROSTHESIS, INTERVERTEBRAL DISC
FDA Adverse Event
Injury
·SYNTHES USA·Product code MJO·October 26, 2016
PROSTHESIS, INTERVERTEBRAL DISC
FDA Adverse Event
Injury
·SYNTHES USA·Product code MJO·October 26, 2016
PROSTHESIS, INTERVERTEBRAL DISC
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code MJO·October 26, 2016
PROSTHESIS, INTERVERTEBRAL DISC
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code MJO·October 26, 2016
GORE TIGRIS® VASCULAR STENT
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code NIP·October 11, 2016
PRIMEADVANCED
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·June 10, 2013
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 13, 2011
WALLSTENT ENTERAL ENDOPROSTHESIS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC IRELAND, LTD.·Product code MQR·September 12, 2008
LUTONIX 035 DRUG COATED BALLOON PTA CATHETER
FDA Adverse Event
Injury
·C.R. BARD, INC. (GFO)·Product code ONU·January 19, 2018
LUTONIX 035 DRUG COATED BALLOON PTA CATHETER
FDA Adverse Event
Injury
·C.R. BARD, INC. (GFO)·Product code ONU·February 9, 2018
LUTONIX 035 DRUG COATED BALLOON PTA CATHETER
FDA Adverse Event
Injury
·C.R. BARD, INC. (GFO)·Product code ONU·February 6, 2018
LUTONIX 035 DRUG COATED BALLOON PTA CATHETER
FDA Adverse Event
Injury
·C.R. BARD, INC. (GFO)·Product code ONU·March 26, 2018
LUTONIX 035 DRUG COATED BALLOON PTA CATHETER
FDA Adverse Event
Injury
·C.R. BARD, INC. (GFO)·Product code ONU·February 14, 2018
GORE TIGRIS® VASCULAR STENT
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code NIP·September 6, 2016