BEUDAMED
    6 results · 36ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SHOCKPULSE LITHOTRIPSY TRANSDUCER.

    FDA Adverse Event
    Malfunction ·GYRUS ACMI, INC.·Product code FEO·January 29, 2025

    SERIES A PAT W/WR THN 28 1 PEG

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·January 12, 2022

    FLEXTEND II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·April 8, 2013

    ACCU-CHEK ® SPIRIT COMBO

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LZG·August 27, 2014

    ALTRUA

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·April 6, 2011

    ONE-LINK NEUTRAL LUER ACTIVATED DEVICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·April 14, 2020