BEUDAMED
    6 results · 19ms · Sources: EU EUDAMED, US FDA

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    KETAC-MOLAR APLICAP

    FDA 510(k)
    FDA Class 2 ·Dental

    MODIFICATION TO ENSITE SYSTEM, MODEL EE3000

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CROWNTEX EXAM. CAPE & GOWN

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SPACEMAKER BLUNT TIP TROCAR 10MM

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY USSC·Product code GCJ·May 23, 2014

    TRILOGY O2

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·January 30, 2013

    NEXGEN CRUCIATE RETAINING ARTICULAR SURFACE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·January 11, 2011