BEUDAMED
    4 results · 68ms · Sources: EU EUDAMED, US FDA

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    PROBE

    FDA Adverse Event
    Malfunction ·COHERENT MEDICAL DIVISION·Product code GEX·July 17, 1996

    ASSURE WEARABLE CARDIOVERTER DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·KESTRA MEDICAL TECHNOLOGIES, INC.·Product code MVK·November 19, 2025

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code CAL·June 19, 2019

    ASAHI PROWATERFLEX PTCA GUIDE WIRE

    FDA Adverse Event
    Malfunction ·AV-ASAHI·Product code DQX·May 3, 2013