BEUDAMED
    61 results · 92ms · Sources: EU EUDAMED, US FDA

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    SCORPION - SUREFIRE NEEDLE

    FDA Adverse Event
    Malfunction ·ARTHREX ARTHROSCOPY INSTRUMENTS, INC.·Product code NBH·February 2, 2009

    LOW PROFILE CANNULA

    FDA Adverse Event
    Malfunction ·ARTHREX ARTHROSCOPY INSTRUMENTS, INC.·Product code HRX·February 26, 2009

    SUREFIRE SCORPION NEEDLE

    FDA Adverse Event
    Malfunction ·ARTHREX ARTHROSCOPY INSTRUMENTS, INC.·Product code HWC·January 15, 2010

    *

    FDA Adverse Event
    Malfunction ·ARTHREX ARTHROSCOPY INSTRUMENTS, INC·Product code MAI·May 15, 2007

    CONTINUOUS WAVE III

    FDA Adverse Event
    ARTHREX ARTHROSCOPY INSTRUMENTS, INC.·Product code HRX·June 21, 2007

    FIBERWIRE

    FDA Adverse Event
    Malfunction ·ARTHREX ARTHROSCOPY INSTRUMENTS, INC.·Product code GAO·May 4, 2007

    *

    FDA Adverse Event
    Malfunction ·ARTHREX ARTHROSCOPY INSTRUMENTS, INC.·Product code NBH·May 31, 2007

    BIO-CORKSCREW

    FDA Adverse Event
    Malfunction ·ARTHREX ARTHROSCOPY INSTRUMENTS, INC.·Product code MBI·June 22, 2007

    *

    FDA Adverse Event
    Malfunction ·ARTHREX ARTHROSCOPY INSTRUMENTS, INC.·Product code NBH·June 15, 2007

    TRIM-IT

    FDA Adverse Event
    Malfunction ·ARTHREX ARTHROSCOPY INSTRUMENTS, INC.·Product code HTW·May 7, 2007

    SCORPION

    FDA Adverse Event
    Injury ·ARTHREX ARTHROSCOPY INSTRUMENTS, INC.·Product code GAB·May 30, 2007

    CONTINUOUS WAVE III

    FDA Adverse Event
    Malfunction ·ARTHREX ARTHROSCOPY INSTRUMENTS, INC.·Product code HRX·December 12, 2008

    SUREFIRE SCORPION NEEDLE

    FDA Adverse Event
    Malfunction ·ARTHREX ARTHROSCOPY INSTRUMENTS, INC.·Product code MFJ·November 25, 2008

    SUREFIRE SCORPION

    FDA Adverse Event
    Malfunction ·ARTHREX ARTHROSCOPY INSTRUMENTS, INC.·Product code GAB·November 19, 2008

    SUREFIRE SCORPION

    FDA Adverse Event
    Malfunction ·ARTHREX ARTHROSCOPY INSTRUMENTS, INC.·Product code MDM·October 23, 2008

    LOW PROFILE CANNULA

    FDA Adverse Event
    Malfunction ·ARTHREX ARTHROSCOPY INSTRUMENTS, INC.·Product code HRX·April 17, 2009

    CONTINUOUS WAVE III

    FDA Adverse Event
    Malfunction ·ARTHREX ARTHROSCOPY INSTRUMENTS, INC.·Product code HRX·April 10, 2009

    BIO-CORKSCREW

    FDA Adverse Event
    Malfunction ·ARTHREX ARTHROSCOPY INSTRUMENTS, INC.·Product code MBI·February 19, 2007

    BIOCORKSCREW

    FDA Adverse Event
    Malfunction ·ARTHREX ARTHROSCOPY INSTRUMENTS, INC.·Product code MBI·February 5, 2007

    BIO-CORKSCREW SUTURE ANCHOR

    FDA Adverse Event
    Malfunction ·ARTHREX ARTHROSCOPY INSTRUMENTS, INC.·Product code MBI·January 31, 2007