BEUDAMED
    566 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    ARRAY SPINAL SYSTEM IMPLANTS AND INSTRUMENTS

    FDA Adverse Event
    Malfunction ·EBI, LLC·Product code KWP·January 10, 2012

    ZYSTON INTERBODY SPACER SYSTEMS

    FDA Adverse Event
    Malfunction ·EBI, LLC·Product code BZD·March 29, 2012

    ENCLAVE ANTERIOR SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·EBI, LLC·Product code MAX·February 14, 2012

    IBEX SPINAL SYSTEM IMPLANTS AND INSTRUMENTS

    FDA Adverse Event
    Malfunction ·EBI, LLC·Product code NKB·February 24, 2012

    ALTIUS OCT POSTERIOR SPINAL SYSTEM IMPLANTS AND INSTRUMENTS

    FDA Adverse Event
    Malfunction ·EBI, LLC·Product code KWP·February 21, 2012

    PHOENIX ANKLE NAIL

    FDA Adverse Event
    Malfunction ·EBI, LLC.·Product code HSB·February 7, 2012

    ARRAY SPINAL SYSTEM IMPLANTS AND INSTRUMENTS

    FDA Adverse Event
    Malfunction ·EBI, LLC·Product code KWP·March 30, 2012

    POLARIS 5.5 STANDARD IMPLANT KIT

    FDA Adverse Event
    Malfunction ·EBI, LLC·Product code HWC·January 18, 2012

    PLUG

    FDA Adverse Event
    Malfunction ·EBI, LLC·Product code MNH·March 21, 2012

    C-TEK MAXAN IMPLANTS

    FDA Adverse Event
    Malfunction ·EBI, LLC·Product code KWQ·March 20, 2009

    ARRAY SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·EBI, LLC·Product code MNI·January 19, 2009

    ARRAY SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·EBI, LLC·Product code MNI·January 19, 2009

    SPF SPINE FUSION STIMULATOR

    FDA Adverse Event
    Malfunction ·EBI, LLC·Product code LOE·March 11, 2010

    C-TEK MAXAN IMPLANTS

    FDA Adverse Event
    Malfunction ·EBI, LLC·Product code KWQ·March 24, 2010

    PHOENIX ANKLE ARTHRODESIS NAIL SYSTEM

    FDA Adverse Event
    Malfunction ·EBI, LLC·Product code HWC·March 17, 2010

    VHS

    FDA Adverse Event
    Malfunction ·EBI, LLC·Product code HSB·February 16, 2010

    ARRAY SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·EBI, LLC·Product code MNI·March 11, 2010

    POLARIS 5.5 DEFORMITY SYSTEM

    FDA Adverse Event
    Malfunction ·EBI, LLC·Product code MNH·March 19, 2010

    BALLISTA INSTRUMENTS

    FDA Adverse Event
    Malfunction ·EBI, LLC·Product code LXH·March 4, 2010

    ARRAY TI IMPLANTS

    FDA Adverse Event
    Malfunction ·EBI, LLC·Product code MNI·March 10, 2010