BEUDAMED
    6 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    DATASCOPE INTRA-AORTIC PUMP

    FDA Adverse Event
    Death ·DATASCOPE CORP.·Product code DSP·May 6, 2014

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·October 31, 2012

    FINNED 1 PIECE TIBIAL TRAY

    FDA Adverse Event
    Injury ·BIOMET SPAIN S.L.·Product code JWH·August 16, 2010

    PEN NDL 32G 4MM PRO 100 BOX 1200 US

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMI·July 30, 2021

    BD NANO¿ 2ND GEN PEN NEEDLES 32G X 4MM (100 COUNT)

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·October 25, 2023

    BD PEN NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·February 23, 2021