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

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    STOPCOCK (ONE-PORT MANIFOLD)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    WI-38 HUMAN LUNG CELLS

    FDA 510(k)
    FDA Class 1 ·Hematology

    Easi-Vue® embolic microspheres System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

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

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

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

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

    STENOSCOP

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 3, 2013

    LIFEPAK CR PLUS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·December 3, 2010

    11/13 S-ROM 40MM M SPEC+9

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. ¿ REG. # 8010379·Product code JDI·July 15, 2014

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