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

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    Filters FDA Adverse Event ×

    BD PLASTIPAK LUER-LOK TIP SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·June 3, 2021

    BCI

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code CCK·November 7, 2021

    8100 ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·December 16, 2020

    BCI CAPNOCHECK SLEEP OXIMETER

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code CCK·September 27, 2019

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·March 12, 2013

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·February 7, 2011

    OBTAPE SLING

    FDA Adverse Event
    Injury ·MENTOR·Product code FTL·February 25, 2008

    466FXXXX

    FDA Adverse Event
    Injury ·CORDIS CASHEL·Product code DTK·November 19, 2018

    SYRINGE NS 1ML LS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·November 26, 2020