BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PATHROMTIN SL

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GFO·August 11, 2017

    ALLOFIT ALLOCLASSIC, PLUGS FOR SCREW HOLES

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code KWA·December 11, 2018

    PATHROMTIN SL

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GFO·August 11, 2017

    PATHROMTIN SL (RILIBAK)

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GFO·January 4, 2023

    HUDSON ET TUBE, UNCUFFED, 2.5

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BTR·June 12, 2014

    NC TENKU DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code LOX·February 11, 2013

    TENDRIL SDX

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·January 10, 2011

    ALLOFIT ALLO-C SCR PLUG STER

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code KWA·December 7, 2018