23 results
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34ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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SMARTSITE NEEDLE FREE VALVE ADMINISTRATION SETS
FDA 510(k)
FDA Class 2
·General Hospital
BD SMARTSITE¿ NEEDLE-FREE CONNECTOR
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·June 13, 2022
BD SMARTSITE¿ NEEDLE-FREE CONNECTOR
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·June 10, 2022
BD ALARIS SMARTSITE NEEDLE-FREE VALVE
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·May 11, 2023
BD SMARTSITE¿ NEEDLE-FREE CONNECTOR
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·July 5, 2022
BD SMARTSITE¿ NEEDLE-FREE CONNECTOR
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·July 8, 2022
BD SMARTSITE¿ NEEDLE-FREE CONNECTOR
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·July 6, 2022
BD ALARIS SMARTSITE NEEDLE-FREE VALVE
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·March 8, 2023
BD ALARIS SMARTSITE NEEDLE-FREE VALVE
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·April 6, 2023
BD ALARIS SMARTSITE NEEDLE-FREE VALVE
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·April 5, 2023
BD SMARTSITE¿ NEEDLE-FREE CONNECTOR
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·November 14, 2022
BD SMARTSITE¿ NEEDLE-FREE CONNECTOR
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·December 22, 2022
BD SMARTSITE¿ NEEDLE-FREE CONNECTOR
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·December 23, 2022
BD ALARIS SMARTSITE NEEDLE-FREE VALVE
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·December 12, 2022
BD SMARTSITE¿ NEEDLE-FREE CONNECTOR, PRIMING VOLUME 0.11 ML
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·November 9, 2022
HI-TORQUE EXTRA S'PORT GUIDEWIRE
FDA 510(k)
FDA Class 2
·Cardiovascular
AMMONIA-L3K ASSAY, MODEL 263-17, AMMONIA-L3K ASSAY, MODEL 263-30
FDA 510(k)
FDA Class 1
·Clinical Chemistry
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR·Product code CBK·April 10, 2013
SCULPTRA
FDA Adverse Event
Injury
·SANOFIAVENTIS U.S. LLC·Product code LMH·April 13, 2011
CRYSTALENS
FDA Adverse Event
Injury
·EYEONICS, INC.·Product code HQL·June 16, 2008