BEUDAMED
    6 results · 23ms · Sources: EU EUDAMED, US FDA

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    UNIVERSAL PLUS ES S/I INSTRUMENT

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

    ENCORE RHEUMATOID FACTOR EIA

    FDA 510(k)
    FDA Class 2 ·Immunology

    NK PINCH SENSOR, MODEL PF002

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COGNIS

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·January 10, 2011

    AUTOPULSE® LI-ION BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC·Product code DRM·July 23, 2014

    PUMP MMT-715NAL PRDGM INS V2.1 CL EN

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code LZG·September 4, 2007