BEUDAMED
    4 results · 35ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    CA-1000

    FDA Adverse Event
    Injury ·TOA MEDICAL ELECTRONICS·Product code GKP·January 6, 1997

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR·Product code CBK·May 30, 2014

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·February 15, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 20, 2011