BEUDAMED
    3 results · 13ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    INTRA-AORTIC BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·DATASCOPE CORPORATION·Product code DSP·February 26, 1998

    S3 EX - 3005

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·October 8, 2012

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·August 29, 2007