BEUDAMED
    13 results · 25ms · Sources: EU EUDAMED, US FDA

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    GEENEN/ZEBRA GUIDELINES

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    TRANSEND EX 14 GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC, NEUROVASCULAR DIVISION·Product code DQX·September 23, 2009

    MALDI Biotyper CA System

    FDA 510(k)
    FDA Class 2 ·Microbiology

    EMIT D.A.U. OPIATE ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Malfunction ·NEUROVASCULAR DIVISION, BOSTON SCIENTIFIC CORP·Product code DQX·October 27, 2009

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 7, 2010

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 10, 2010

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·July 14, 2010

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 10, 2010

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 27, 2015

    ALLURA XPER FD20

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code IZI·December 8, 2010

    2.5MM DHS/DCS GUIDE WIRE W/THREADED TIP 230MM

    FDA Adverse Event
    Malfunction ·SYNTHES BALSTHAL·Product code LRN·July 17, 2014

    TRANSEND GUIDEWIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·May 27, 2010