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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    ZCH ALPHA SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SYSMEX NE-1500, MODIFICATION

    FDA 510(k)
    FDA Class 2 ·Hematology

    MIDMARK MAGNUM GENERAL SURGICAL TABLE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD·Product code MCM·February 11, 2013

    ROTABLATOR ROTATIONAL ATHERECTOMY SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - FREMONT (CE)·Product code MCX·July 24, 2014

    PROMOTE ACCEL CRT-D

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·January 10, 2011