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

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    DATA-FI FIBRIN(OGEN) DEGRADATION PROD.(FDP)DET SET

    FDA 510(k)
    FDA Class 2 ·Hematology

    ARRHYTHMIA MODULE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    K-Y BRAND INTRIGUE INTENSE WARMING SENSATION

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR·Product code CBK·April 18, 2014

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·December 13, 2012

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·October 11, 2010