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

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    Filters Status: Malfunction ×

    THUNDERBEAT 5 MM, 35 CM, FRONT-ACTUATED GRIP

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEM CORP·Product code GEI·March 13, 2014

    LIFEVEST WCD 3100 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·September 3, 2010

    PULSE GENERATOR, PERMANENT, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code NVZ·May 1, 2018

    ALINITY M HR HPV AMP KIT

    FDA Adverse Event
    Malfunction ·ABBOTT MOLECULAR, INC.·Product code MAQ·February 26, 2024

    PULSE GENERATOR, PERMANENT, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code NVZ·December 22, 2016

    NAVITOR TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL·Product code NPT·May 28, 2026