BEUDAMED
    15 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    HEARTSTART MRX -EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 1, 2020

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·April 6, 2026

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·April 6, 2026

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·April 6, 2026

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·April 6, 2026

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·April 6, 2026

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·April 6, 2026

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·April 6, 2026

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·April 6, 2026

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·April 6, 2026

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·April 6, 2026

    IMMULITE 2000

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS·Product code JJQ·March 27, 2013

    OT ULTRA METER

    FDA Adverse Event
    Injury ·LIFESCAN INC.·Product code NBW·March 17, 2011

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·April 1, 2008

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Injury ·INSULET CORPORATION·Product code LZG·September 29, 2022