BEUDAMED
    5 results · 27ms · Sources: EU EUDAMED, US FDA

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    INTRA-AORTIC BALLOON CATHETER

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

    SUPERION INDIRECT DECOMPRESSION SYSTEM

    FDA Adverse Event
    Injury ·VERTIFLEX INC.·Product code NQO·September 3, 2020

    3M SCOTCAST WET OR DRY CAST PADDING

    FDA Adverse Event
    Injury ·3M HEALTH CARE·Product code ITG·April 30, 2014

    IN TOUCH EC MARK

    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