BEUDAMED
    5 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·June 18, 2024

    VORTEX

    FDA Adverse Event
    Injury ·ANGIODYNAMICS, INC.·Product code LJT·March 18, 2026

    SELECT SECURE

    FDA Adverse Event
    Malfunction ·MPRI·Product code NVY·March 7, 2013

    COLLEAGUE SINGLE CHANNEL VOLUMETRIC PUMP CE FRENCH

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·February 16, 2011

    MEDTRONIC LEAD

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code DXY·August 8, 2014