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

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    INTERSEAL ACETABULAR SCREW HOLE PLUG

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PEEK Corpectomy

    FDA UDI
    Nuvasive, Inc.·00887517623843·PEEK Corp Core, Ø14x29mm

    DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code PQF·December 19, 2019

    TI2200 TRANSILLUMINATION CABLE

    FDA 510(k)
    FDA Class 2 ·Dental

    Magnetic Surgical System

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    BD VACUTAINER® K2 EDTA (K2E) 10.8 MG BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·May 22, 2018

    VITROS ECIQ IMMUNODIAGNOSTIC SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KHO·February 21, 2013

    PD CYCLER 110 VOLT HOME CHOICEPRO AUTOMATED

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·January 27, 2011

    HEARTWARE® VENTRICULAR ASSIST SYSTEM

    FDA Adverse Event
    Malfunction ·HEARTWARE, INC·Product code DSQ·July 31, 2014