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

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    ISSYS LP SPINAL FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·July 13, 2007

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code GJS·November 19, 2007

    WALLSTENT ENTERNAL PROSTHESIS

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MEROX BIPOLAR HIGH IMPEDANCE LEAD MODELS: MEX 53/13-BP; 60/15-BP; 45-JBP; 53-JBP

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·August 20, 2007

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·July 27, 2007

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, SJ·Product code JPA·January 11, 2008

    WALLFLEX ESPOHAGEAL PARTIALLY COVERED STENT

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC, INC.·Product code ESW·March 19, 2013

    UNKNOWN PREFILL

    FDA Adverse Event
    Death ·COVIDIEN·Product code NZW·April 20, 2011

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·July 9, 2008

    BIOMET CC CRUCIATE TRAY

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 5, 2018