BEUDAMED
    8 results · 16ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    1051786-2019-00015

    FDA Adverse Event
    Malfunction ·April 10, 2019

    XPER FLEX CARDIO PHYSIOMONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·INVIVO CORPORATION·Product code MWI·October 25, 2019

    BILITX LIGHT SOURCE

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code LBI·August 23, 2016

    INTELLIVUE X3

    FDA Adverse Event
    Malfunction ·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code MHX·May 23, 2025

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code FSA·April 10, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·April 12, 2011

    INTELLIVUE MULTI-MEASUREMENT MODULE X3

    FDA Adverse Event
    Malfunction ·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code MHX·May 19, 2026

    EXPRESSION PATIENT MONITOR (MR400)

    FDA Adverse Event
    Malfunction ·INVIVO, A DIVISION OF PHILIPS MEDICAL SYSTEMS·Product code MWI·September 5, 2023