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

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    STERITEC DRY HEAT INDICATOR LABEL

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Endoskeleton(r) TCS System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Sim&Size

    FDA 510(k)
    FDA Class 2 ·Radiology

    MAXIMO II VR

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code LWS·February 9, 2013

    PRECISION OPTIUM EZ

    FDA Adverse Event
    Malfunction ·Product code NBW·January 7, 2011

    NC QUANTUM APEX?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LOX·July 23, 2014

    EVOLUT FX DCS

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code NPT·August 8, 2025

    UNK - VEPTR IMPLANTS: PARALLEL CONNECTOR

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code MDI·December 9, 2019