BEUDAMED
    34 results · 32ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PLASTIPAK LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·March 31, 2026

    BD PLASTIPAK LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 30, 2026

    BD PLASTIPAK LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 20, 2026

    BD PLASTIPAK LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 8, 2026

    BD PLASTIPAK LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·March 20, 2026

    BD PLASTIPAK LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·March 19, 2026

    BD PLASTIPAK LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 23, 2026

    BD PLASTIPAK LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 29, 2026

    BD PLASTIPAK LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 24, 2026

    BD PLASTIPAK LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 27, 2026

    CMF CUSTOMIZED IMPLANT KIT LARGE

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code KKY·March 7, 2013

    BD PLASTIPAK LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 22, 2026

    BD PLASTIPAK LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 15, 2026

    BD PLASTIPAK LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·March 19, 2026

    BD PLASTIPAK LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 16, 2026

    BD PLASTIPAK LUER-LOK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 15, 2026

    IMP,TSV,4.1MM,SBM,13

    FDA Adverse Event
    Injury ·ZIMVIE US CORP LLC·Product code DZE·October 21, 2025

    MED-EL MAESTRO COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·MED-EL ELEKTROMEDIZINISCHE GERAETE, GMBH·Product code MCM·April 24, 2013

    COR31 12X150MM, KII OPTICAL ACCESS SYSTEM

    FDA Adverse Event
    Malfunction ·INTUITIVE·Product code GCJ·April 28, 2011

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD/HUNTINGTON·Product code HQL·July 25, 2008