BEUDAMED
    3 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    UNKNOWN DEPUY ASR ACETABULAR CUP

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD - 8010379·Product code KWA·April 30, 2014

    LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code LDD·October 10, 2012

    LINOX SD 65/16

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVY·July 29, 2010