BEUDAMED
    7 results · 25ms · Sources: EU EUDAMED, US FDA

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    AIA-PACK IGE CALIBRATION VERIFICATION TEST SET

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    BARTRONIX IN-BED ACTIVITY MONITOR

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MOTOR DRIVEN EXTIRPATION INSTRUMENTS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EDWARDS SAPIEN 3 TRANSCATHETER HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES LLC·Product code NPT·December 17, 2018

    PRIME ZOOM STRETCHER,30"LITTER

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code INK·January 22, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·February 5, 2014

    STANDARD LAG SCREW OMEGA 80MM LENGTH

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS SELZACH·Product code KTT·December 8, 2010