BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    SYNAPSE SYSTEM, SYNTHES OC FUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ORTHOSIS,PEDICLE SPINAL FIXATION

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

    ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DDD

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

    HERMETIC LUMBAR CATHETER, OPEN TIP

    FDA Adverse Event
    Injury ·INTEGRA NEUROSCIENCES PR·Product code JXG·September 2, 2015

    ABL90

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    MAYFIELD ACCISS II IMAGE GUIDED SURGERY SYSTEM, MODEL 2002-01

    FDA 510(k)
    FDA Class 2 ·Neurology

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 4, 2014

    LAMITRODE TRIPOLE 16

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 28, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 28, 2011

    3 ML BD PRESET¿ SYRINGE WITH BD LUER-LOK¿ TIP, 23 G X 1 IN BD ECLIPSE¿ NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·January 23, 2017