BEUDAMED
    7 results · 20ms · Sources: EU EUDAMED, US FDA

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    ACS HI-TORQUE GUIDE WIRE

    FDA Adverse Event
    Injury ·GUIDANT, ADVANCED CARDIOVASCULAR SYSTEMS·Product code DQX·February 13, 2002

    DEPTH DEVICE, 2.7 / 3.5 / 4.0MM, LOW PRO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HTJ·February 3, 2025

    AGILTRAC .035 PERIPHERAL DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR-VASCULAR SOLUTIONS·Product code LIT·August 25, 2008

    DEPTH DEVICE, 2.7 / 3.5 / 4.0MM, LOW PRO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HTJ·February 6, 2025

    T-SLING

    FDA Adverse Event
    Injury ·HERNIAMESH S.R.L.·Product code PAH·March 7, 2013

    SAFE-T-PRO PLUS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·March 9, 2011

    CHARITE ARTIFICIAL DISC, SIZE UNK

    FDA Adverse Event
    Injury ·DEPUY SPINE, INC.·Product code MJO·February 12, 2008