BEUDAMED
    6 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    GUIDEWIRE INTRODUCER SET

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EXIT ALARM

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SATURATION/HEMATOCRIT MONITOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    INFUSOMAT SPACE

    FDA Adverse Event
    Malfunction ·B. BRAUN MEDICAL, INC.·Product code FRN·November 5, 2010

    CATHETER AND CANNULA

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DWF·January 9, 2013

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·July 7, 2014