BEUDAMED
    9 results · 37ms · 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 FDA Adverse Event ×

    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

    LONG NAIL KIT R1.5, TI, LEFT GAMMA3 10X260MM X 12

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·September 6, 2012

    EASYTRAK 2

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code OJX·January 11, 2013

    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