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

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    Filters Status: Malfunction ×

    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

    SAFE-T-PRO PLUS

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