BEUDAMED
    14 results · 21ms · Sources: EU EUDAMED, US FDA

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    VITAL-PORT MINI VASCULAR ACCESS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DWF CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS

    FDA Adverse Event
    Injury ·COOK VASCULAR INC·Product code DWF·December 15, 2016

    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 EX 14 GUIDEWIRE

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

    CANARY BREATHING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    CORRESTORE PATCH SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    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 10, 2010

    TRANSEND GUIDEWIRE

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

    CORAIL AMT COLLAR SIZE 8

    FDA Adverse Event
    Injury ·DEPUY FRANCE S.A.S.-SAINT PRIEST·Product code KWA·January 28, 2013

    ATLANTIS SR PRO2 CORONARY IMAGING CATHETER, MODEL 39014

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - FREMONT·Product code DQO·December 17, 2010

    M2A-MAGNUM PF CUP 48ODX42ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·July 14, 2014