BEUDAMED
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    MNI 400 INJECTION CAPS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    MNI, MNH

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code MNI·February 13, 2013

    MNI, MNH

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code MNI·February 13, 2013

    MNI, MNH

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code MNI·February 13, 2013

    MNI, MNH

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code MNI·February 13, 2013

    MNI, MNH

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code MNI·February 13, 2013

    EON MNI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·October 25, 2013

    KWP, MNH, MNI

    FDA Adverse Event
    Injury ·ALPHATEC SPINE INC·Product code KWP·August 13, 2015

    NKB, MNH, MNI

    FDA Adverse Event
    Malfunction ·ALPHATEC SPINE INC·Product code NKB·September 30, 2015

    EX-PRES MNI GLAUCOMA SHUNT

    FDA Adverse Event
    Malfunction ·OPTONOL LTD.·Product code KYF·March 2, 2012

    MST/DEWEY MNI PHACO TIP 30DEG

    FDA Adverse Event
    Malfunction ·MICROSURGICAL TECHNOLOGY, INC.·Product code HQC·August 28, 2014

    ARRAY TITANIUM IMPLANTS

    FDA Adverse Event
    Malfunction ·BIOMET·Product code MNI·April 17, 2009

    PEN NEEDLE 31G 5 MM 3/16" MNI

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·May 18, 2022

    ORTHOSIS,PEDICLE SPINAL FIXATION

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MNI·December 8, 2015

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MBX·January 27, 2022

    ENDOPATH ENDOSCOPIC LINEAR CUTTER - ETS45MM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code KOG·July 21, 2004

    ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DDD

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·March 25, 2015

    APPLIANCE, FIXATION, SPINAL INTERLAMINAL

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KWP·April 7, 2016

    REVERE

    FDA Adverse Event
    Injury ·GLOBUS MEDICAL, INC.·Product code KWQ·January 30, 2017

    TI NUT 11MM WIDTH ACROSS FLATS

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code KWP·October 9, 2015