BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    T-CONNECTOR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    VuePoint

    FDA UDI
    Nuvasive, Inc.·00887517338006·VuePoint Screw, 4.5x8mm Occipital

    MODIFICATION TO: DSS STABILIZATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Spinal Fixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RSP SHOULDER

    FDA Adverse Event
    Injury ·ENCORE MEDICAL, L.P.·Product code KWS·May 5, 2014

    EXTERNAL PULSE GENERATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA INC.·Product code DTE·October 15, 2012

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·August 2, 2007

    BD ALARIS¿ EXTENSION SET

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·November 24, 2021

    UNSPECIFIED BD INFUSION SET

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·December 22, 2022