BEUDAMED
    4 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    CROSSER RECANALIZATION CATHETER

    FDA Adverse Event
    Death ·BARD PERIPHERAL VASCULAR, INC.·Product code PDU·May 1, 2014

    LIFEVEST WCD 3100 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·October 12, 2012

    PLM A+ PLATINUM MODU

    FDA Adverse Event
    Malfunction ·HOSPIRA, INC.·Product code FRN·August 10, 2010

    AURICAL AUD/PMM, 1081

    FDA Adverse Event
    Malfunction ·NATUS MEDICAL DENMARK·Product code EWO·September 23, 2020