10,000 results
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47ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CONDUCTIVE HYDROGEL POLYMER BASED ON U & C SERIES ELECTRODES
FDA 510(k)
FDA Class 2
·Cardiovascular
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS CORPORATION·Product code NIQ·January 19, 2015
STENT CORONARY
FDA Adverse Event
Death
·CORDIS CORPORATION·Product code MAF·March 25, 2015
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS CORPORATION·Product code NIQ·January 19, 2015
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS CORPORATION·Product code NIQ·January 19, 2015
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS CORPORATION·Product code NIQ·October 10, 2014
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS CORPORATION·Product code NIQ·October 23, 2014
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS CORPORATION·Product code NIQ·October 23, 2014
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS CORPORATION·Product code NIQ·October 23, 2014
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS CORPORATION·Product code NIQ·October 23, 2014
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS CORPORATION·Product code NIQ·October 23, 2014
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS LLC (PR)·Product code NIQ·September 24, 2014
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS LLC (PR)·Product code NIQ·September 24, 2014
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS CORPORATION·Product code NIQ·October 23, 2014
INSULIN U -500
FDA Adverse Event
Injury
·LILLY·Product code FMF·December 1, 2010
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS CORPORATION·Product code NIQ·October 10, 2014
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS CORPORATION·Product code NIQ·September 15, 2015
PALMAZ-SCHATZ BALLOON EXPANDABLE STENT WITH DELIVERY SYSTEM
FDA Adverse Event
Injury
·CORDIS CORPORATION·Product code MAF·June 14, 2011
S.M.A.R.T. NITINOL STENT SYSTEM
FDA Adverse Event
Injury
·CORDIS CORPORATION·Product code FGE·February 6, 2015
ADVANTAGE SERIES 26
FDA Adverse Event
Malfunction
·STRYKER CORP., MEDICAL DIVISION·Product code FPO·November 19, 2010