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

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    EXCELSIOR 1018 MICROCATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EXCELSIOR SL-10 MICROCATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC, NEUROVASCULAR DIV.·Product code DQY·July 10, 2009

    EXCELSIOR SL-10 PRE-SHAPED 45 CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION, NEUROVASCULAR DIVISION·Product code DQO·December 12, 2007

    EXCELSIOR SL-10 PRE-SHAPED 45 DEGREES MICROCATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION, NEUROVASCULAR DIV·Product code DQO·April 25, 2007

    EXCELSIOR SL-10 PRE-SHAPED 45 DEGREES MICROCATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION, NEUROVASCULAR DIVISION·Product code DQO·November 14, 2007

    EXCELSIOR SL-10 MICROCATHETER

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC CORPORATION·Product code DQO·May 1, 2007

    EXCELSIOR SL-10 PRE-SHAPED CATHETER

    FDA Adverse Event
    Malfunction ·NEUROVASCULAR, A DIV. OF BOSTON SCIENTIFIC CORP·Product code DQO·September 14, 2006

    EXCELSIOR SL-10 MICROCATHETER

    FDA Adverse Event
    Malfunction ·NEUROVASCULAR, A DIV OF BOSTON SCIENTIFIC CORP·Product code DQO·January 3, 2007

    EXCELSIOR SL-10 MICROCATHETER

    FDA Adverse Event
    Death ·BOSTON SCIENTIFIC CORP., NEUROVASCULAR DIV·Product code DQO·September 15, 2006

    EXCELSIOR SL-10 PRE-SHAPED 45 DEGREES MICROCATHER

    FDA Adverse Event
    Malfunction ·NEUROVASCULAR, DIVISION OF BOSTON SCIENTIFIC CORPORATION·Product code DQO·January 3, 2007

    EXCELSIOR SL-10 PRE-SHAPED J MICROCATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC, NEUROVASCULAR DIVISION·Product code DQO·August 17, 2007

    EXCELSIOR SL-10 MICROCATHETER

    FDA Adverse Event
    Malfunction ·NEUROVASCULAR, A DIV OF BOSTON SCIENTIFIC CORP·Product code DQO·September 14, 2006

    EXCELSIOR 1018 MICROCATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORP, NEUROVASCULAR·Product code FOZ·August 2, 2006

    MEDILAS 4060N FIBERTOM(R) SURGICAL LASER

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

    SLEEPSCAN

    FDA 510(k)
    FDA Class 2 ·Neurology

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 13, 2013

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·February 16, 2011

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·August 8, 2014

    STERRAD® NX STERILIZER

    FDA Adverse Event
    Malfunction ·ADVANCED STERILIZATION PRODUCTS·Product code MLR·February 20, 2018