BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    CREATININE (ENZYMATIC)

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ABBOTT TUBE EDTA PLH 13X75 2.0 PNK

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·August 3, 2022

    ABBOTT TUBE EDTA PLH 13X75 2.0 PNK

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·September 17, 2019

    PERSONAL INFUSOR LOCAL PAIN MANAGEMENT PROCEDURAL KIT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PERCUTANEOUS INTRODUCER, MODEL 10383-XXX

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PROMUS ELEMENT ¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·April 22, 2013

    MICRO DRILL MEDIUM STRAIGHT ATTACHMENT

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code DZJ·April 15, 2011

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS, INC.·Product code JAA·July 9, 2008

    ARCHITECT SIROLIMUS

    FDA Adverse Event
    Malfunction ·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code NRP·February 5, 2026