BEUDAMED
    8 results · 38ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SYRINGE 0.3ML 30GA 1/2IN UF

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·March 14, 2020

    BD INSULIN SYRINGE WITH THE BD ULTRA-FINE NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·October 24, 2019

    INFINION 16

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·February 3, 2021

    AUTOPULSE RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·June 3, 2013

    AUTOPULSE LI-ION BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·May 23, 2013

    XIENCE PRIME LL EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIQ·May 14, 2013

    DUROM ACETABULAR COMPONENT 52/46 L

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·September 10, 2014

    ATTAIN ABILITY

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code OJX·June 3, 2011