BEUDAMED
    9 results · 17ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·March 30, 2026

    DRIVER SHAFT, T-15, LONG

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 14, 2021

    DRIVER SHAFT, T-15, LONG

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 14, 2021

    DRIVER SHAFT, T-15, MEDIUM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 14, 2021

    DRIVER SHAFT, T-15, MEDIUM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 14, 2021

    DRIVER SHAFT, T-15, MEDIUM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 14, 2021

    3.0MM HEX DRIVER

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 14, 2021

    DRIVER SHAFT, T-15, MEDIUM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 14, 2021

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR·Product code CBK·March 11, 2013