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

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    9.5 FR SENSATION DL INTRA-AORTIC BALLON CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Voxel Dosimetry (00859873006226)

    FDA 510(k)
    FDA Class 2 ·Radiology

    SPOTTEST LOEFFLER METHYLENE BLUE STAIN

    FDA 510(k)
    FDA Class 1 ·Hematology

    UNK CAPIOX ARTERIAL FILTER

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTM·April 8, 2019

    PROMUS ELEMENT PLUS EVEROLIMUS-ELUTING PLATINUM CHROMIUM CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·February 5, 2013

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMS, INNOVATION CTR. - SILICON VALLEY·Product code GEX·December 1, 2010

    FORTIFY DR, DF-4 CONNECTOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·July 18, 2014

    CAPIOX ARTERIAL FILTER

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTM·October 10, 2018

    ARTERIAL FILTER

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTM·June 28, 2019