BEUDAMED
    7 results · 25ms · Sources: EU EUDAMED, US FDA

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    CPR MICROMASK

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    KODAK DIRECTVIEW DR SYSTEM DETECTOR

    FDA 510(k)
    FDA Class 2 ·Radiology

    Biomet Spine Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·RICE CREEK MFG·Product code DXY·February 9, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·January 6, 2011

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 22, 2014

    2.7/3.5MM VA-LCP ANTEROLATERAL DISTAL TIBIA PL/10 H/RT-STER

    FDA Adverse Event
    Injury ·SYNTHES ELMIRA·Product code HRS·June 16, 2017