BEUDAMED
    13 results · 39ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    EASYTRAK 2

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code OJX·July 20, 2011

    HEARTMATE LVAS

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·June 7, 2013

    OLYMPUS

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code FDF·September 12, 2008

    OSTEO-SITE BONE BIOPSY NEEDLE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KNW·July 18, 2019

    OSTEO-SITE BONE BIOPSY NEEDLE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KNW·June 17, 2019

    PINNACLE MTL INS NEUT36IDX54OD

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code KWA·March 3, 2014

    ARTICULEZE M HEAD 36MM +8.5

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code JDI·March 3, 2014

    OSTEO-SITE BONE BIOPSY NEEDLE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KNW·January 23, 2019

    OSTEO-SITE BONE BIOPSY NEEDLE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KNW·July 16, 2019

    OSTEO-SITE BONE BIOPSY NEEDLE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KNW·October 8, 2019

    TI LOCKING SCREW

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code NKG·April 5, 2019

    OSTEO-SITE BONE BIOPSY NEEDLE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KNW·July 17, 2019

    OSTEO-SITE BONE BIOPSY NEEDLE

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KNW·July 11, 2019