BEUDAMED
    7 results · 23ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Status: Malfunction ×

    ASSEMBLY FIXTURE M12

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FPA·March 14, 2021

    POLARIS ULTRA

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FAD·June 27, 2019

    SYRINGE SOLOSHOT IX 1ML 22GA 1IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMI·May 28, 2021

    BD PLASTIPAK HYPODERMIC LUER-LOK SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·February 18, 2020

    HEARTSTART FRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·February 24, 2014

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·November 1, 2010

    ASSEMBLY FIXTURE M12

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code ONB·March 25, 2021