BEUDAMED
    8 results · 22ms · Sources: EU EUDAMED, US FDA

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    KINETIC TECHNOOGY PRECISION ADJUSTOR MODEL SHLCP-1

    FDA 510(k)
    FDA Unclassified ·Unknown

    MCKESSON

    FDA Adverse Event
    Malfunction ·MCKESSON MEDICAL-SURGICAL INC.·Product code FMI·January 10, 2020

    INSTANT-VIEW TCA URINE TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    Single-use medical latex examination gloves (LG100)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 13, 2010

    ENDURANT ABDOMINAL STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·January 18, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·January 14, 2014

    ev3 Pipeline Flex Embolization Device with Shield Technology. Sold OUS. For neurological endovascular use.

    FDA Enforcement
    Class I ·Terminated·Micro Therapeutics Inc, Dba Ev3 Neurovascular·April 1, 2020