BEUDAMED
    6 results · 36ms · 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 ×

    SYRINGE S2 5ML 22GA 1-1/4IN BD CHINA

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·December 10, 2019

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILLROM DE MEXICO S DE RL DE CV·Product code FPO·April 10, 2014

    UNKNOWN OMNIFIT H A STEM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code KWY·October 18, 2012

    PREMIUM PLUS CEEA 31 INSTR. W/TILT-TOP

    FDA Adverse Event
    Injury ·USSC PUERTO RICO·Product code GDW·August 17, 2010

    LOGIC CC TIB INSERT SIZE 2, 17MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 10, 2024

    BD SYRINGE S2 5ML 22GA 1-1/4IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·October 29, 2019