BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    21-2120-0103-01

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FRN·November 26, 2024

    ALARIS PCA MODULE SET

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FPA·June 27, 2016

    ALARIS PCA MODULE SET

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FPA·June 27, 2016

    VOLUME VIEW SENSOR

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES DR·Product code DRS·January 24, 2024

    ALARIS PCA MODULE SET

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FPA·June 27, 2016

    AXSYM DIGOXIN III

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code KXT·May 11, 2007

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·March 1, 2011

    MESH -VENTRALEX

    FDA Adverse Event
    Malfunction ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·July 25, 2017