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

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    Filters Status: Malfunction ×

    INTRA-AORTIC BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·August 27, 1998

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·September 21, 2007

    ALL-IN-ONE CCU+LIGHT ROW

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code FCW·July 28, 2020