492 results
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42ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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COMPUTER MD
FDA registration
COMPUTER MD·3 products·🇺🇸 United States
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·June 30, 2016
EVIS EXERA III COLONOVIDEOSCOPE
FDA Adverse Event
Malfunction
·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code FDF·March 25, 2021
COREVALVE REVALVING SYSTEM
FDA Adverse Event
Death
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·October 5, 2016
DURAN ANCORE RING
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code KRH·July 20, 2016
PDS PLATE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code NHB·October 22, 2019
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code NIQ·August 29, 2011
EDWARDS SAPIEN TRANSCATHETER HEART VALVE UNKNOWN
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·August 19, 2020
PROTEGE RX CAROTID STENT SYSTEM
FDA Adverse Event
Injury
·COVIDIEN·Product code NIM·September 24, 2018
VALIANT CAPTIVIA - FF
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·July 27, 2017
UNK-CV-SR-ENDURANT
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·May 18, 2015
TALENT AAA STENT GRAFT
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR·Product code MIH·May 18, 2015
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·March 31, 2016
MANDIBLE DISTRACTION DEVICE
FDA Adverse Event
Injury
·Product code MQP·April 30, 2014
SCREW FIXATION BONE
FDA Adverse Event
Malfunction
·Product code HWC·May 1, 2014
UNKNOWN KNEE TIBIAL TRAY
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JWH·October 18, 2019
ANCURE ENDOGRAFT
FDA Adverse Event
Injury
·GUIDANT ENDOVASCULAR SOLUTIONS·Product code MIH·July 2, 2009
UNKNOWN HIP ACETABULAR LINERS
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code KWA·January 28, 2020
TALENT TAA STENT GRAFT
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR SANTA ROSA·Product code MIH·September 10, 2015
VALIANT STENT GRAFT
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·September 10, 2015