BEUDAMED
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    LMI THROMBECTOMY CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970657·anteriors; shade A3.5 light; mould UCL

    GENERATOR, PULSE, CARDIAC 2LU

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    GETINGE 633HC SERIES VACUUM/GRAVITY STEAM STERILIZER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    E-CAM COINCIDENCE MODE [510 (K) K970627)

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SYSTEMS, INC., NMG GROUP·Product code IYX·April 20, 2001

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code LWP·August 5, 2015

    MBT REVISION CEM TIB TRAY SZ 2

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.1818910·Product code NJL·July 31, 2014

    FREESTYLE FREEDOM LITE

    FDA Adverse Event
    Malfunction ·Product code NBW·January 25, 2011