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

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    Filters FDA Adverse Event ×

    SUPERION INDIRECT DECOMPRESSION SYSTEM

    FDA Adverse Event
    Injury ·VERTIFLEX INC.·Product code NQO·December 1, 2020

    INTRA-AORTIC BALLOON CATHETER

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

    DUAL MOBILITY - UHMWPE

    FDA Adverse Event
    Injury ·LIMACORPORATE SPA·Product code LZO·January 29, 2020

    BD ULTRA FINE-II INSULIN SYRINGE

    FDA Adverse Event
    Injury ·BD·Product code FMF·May 1, 2014

    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