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

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    QTEXX POWDERFREE LATEX EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Cios Select

    FDA 510(k)
    FDA Class 2 ·Radiology

    AMNISURE FETAL MEMBRANES RUPTURE TEST, MODEL FMRT-1

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    AIRVANCE BONE SCREW (REPOSE) SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED INC.·Product code LRK·March 3, 2014

    AIRVANCE BONE SCREW (REPOSE) SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC·Product code LRK·March 29, 2013

    BASIS¿ SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC·Product code KWP·July 19, 2012

    FENESTRATED BIPOLAR FORCEPSINSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·February 27, 2013

    OT ULTRA METER

    FDA Adverse Event
    Injury ·LIFESCAN INC.·Product code NBW·February 8, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·August 5, 2014

    AIRVANCE¿ THS SYSTEM - BONE SCREW WITH SUTURE

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED INC.·Product code LRK·November 30, 2015

    AIRVANCE¿ THS SYSTEM - TOUNGE SUSPENSION KIT

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code LRK·October 2, 2015