BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PREMICATH PICC

    FDA Adverse Event
    Malfunction ·VYGON GMBH·Product code LJS·May 20, 2015

    PREMICATH PICC

    FDA Adverse Event
    Malfunction ·VYGON GMBH·Product code LJS·May 22, 2015

    PREMICATH

    FDA Adverse Event
    Malfunction ·VYGON GMBH·Product code LJS·April 20, 2015

    PREMICATH

    FDA Adverse Event
    VYGON GMBH·Product code LJS·April 20, 2015

    PREMICATH PICC

    FDA Adverse Event
    Malfunction ·VYGON GMBH·Product code LJS·June 3, 2015

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code LWP·February 9, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·January 7, 2011

    ARTICULEZE M HEAD 36MM +5

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD.8010379·Product code JDI·July 23, 2014