BEUDAMED
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    Filters FDA Adverse Event ×

    FEMORAL HEAD BIOLOX DELTA CERAMIC 12/14 - 36 S

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code LZO·June 20, 2022

    DYNASTY® A-CLASS® STD POLY LINER 36MM GROUP G

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code JDI·June 20, 2022

    VITALITY 2

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 19, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 27, 2014

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·December 14, 2012