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

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    ULTRACELL SUCTION SPONGE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Triathlon® X3® UHMWPE Tibial Inserts and Patellar Components

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EMG TRITON -COMP,MODEL NCA01-XXX SERIES

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    XENIUM XPM

    FDA Adverse Event
    Malfunction ·NIPRO CORPORATION *USD*·Product code KDI·February 21, 2013

    OPTA PRO PTA DILATATION CATHETER

    FDA Adverse Event
    Injury ·CORDIS EUROPA, N.V.·Product code LIT·January 28, 2011

    UNIDENTIFIED INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWY·August 1, 2014

    COULTER ACT PAK REAGENT KIT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·September 24, 2014

    COULTER ACT PAK REAGENT KIT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·May 26, 2015

    COULTER ACT PAK REAGENT KIT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·May 5, 2015