BEUDAMED
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    DRAGER INFANT RADIANT WARMERN RH600

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Cryocare CS Surgical System

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

    Swoop® Portable MR Imaging® System

    FDA 510(k)
    FDA Class 2 ·Radiology

    SIMON NITINOL FILTER

    FDA Adverse Event
    Injury ·NITINOL MEDICAL TECHNOLOGIES, INC.·Product code DTK·September 23, 1996

    GENESIS FE 500

    FDA Adverse Event
    Malfunction ·TECAN SCHWEIZ·Product code JQW·June 12, 2014

    ELECTRODE, PACEMAKER, PERMANENT

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·February 9, 2013

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·January 5, 2011