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

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    Filters Regulation: Us FDA ×

    Atrauman® Ag

    FDA 510(k)
    FDA Unclassified ·Unknown

    ADVIA Centaur HAV total assay

    FDA 510(k)
    FDA Class 2 ·Microbiology

    POLYTECH PULMONARY FUNCTION FILTER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ACTIVE CORD

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code KNS·November 11, 2014

    RIATA ST OPTIM ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·September 10, 2011

    GYNECARE TVT OBURATOR SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·July 23, 2013

    BD¿ BLUNT FILL NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code GAA·December 19, 2018

    BD NDLE 18GA 1-1/2IN BLT FILL NC TW SHLD

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·March 6, 2019

    Model Number L111, ESSENTIO DR SL MRI Pacemaker

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025