BEUDAMED
    7 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    VERSA-DIAL 46X24X47 HUM HEAD

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWS·April 24, 2013

    CAPSURE EPI

    FDA Adverse Event
    Injury ·RICE CREEK MFG·Product code NVN·May 8, 2013

    MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·MED-EL ELEKTROMEDIZINISCHE GERAETE GMBH·Product code MCM·May 13, 2011

    TRIFURCATED POSIFLOW EXTENSION SET

    FDA Adverse Event
    Malfunction ·MPS ACACIA·Product code FPA·July 25, 2008

    PC HYBRID GLENOID POST- POLY

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWS·February 28, 2013

    SM HYBRID GLENOID BASE 4MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWS·February 28, 2013

    ADVIA CENTAUR XPT HEPATITIS B SURFACE ANTIGEN II (HBSII)

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code LOM·May 14, 2021