BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ENDO GIA

    FDA Adverse Event
    Injury ·US SURGICAL PUERTO RICO·Product code GDW·September 5, 2018

    QUATTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·October 2, 2012

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·September 18, 2007

    MO.MA. ULTRA 6F ID

    FDA Adverse Event
    Malfunction ·INVATEC SPA·Product code NTE·April 25, 2014

    FILIFORM DOUBLE PIGTAIL URETERAL STENT SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·June 30, 2022

    FILIFORM DOUBLE PIGTAIL URETERAL STENT SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·June 30, 2022

    BLACK SILICONE FILIFORM DOUBLE PIGTAIL URETERAL STENT

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·January 31, 2023

    FILIFORM DOUBLE PIGTAIL URETERAL STENT SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FAD·January 2, 2020

    18.0MM REAMER HEAD FOR RIA 2 STERILE

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HTO·January 7, 2021