BEUDAMED
    7 results · 23ms · Sources: EU EUDAMED, US FDA

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    E-CUBE 8

    FDA 510(k)
    FDA Class 2 ·Radiology

    FLEXITIME XTREME 2 HEAVY TRAY CARTRIDGE REFILL, FEXITIME XTREME 2 LIGHT TRAY CARTRIDGE REFILL

    FDA 510(k)
    FDA Class 2 ·Dental

    PULSE OXIMETER MODEL AB-F1/AH-S1/AH-M1

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    INVICTUS SPINAL FIXATION SYSTEM

    FDA Adverse Event
    Injury ·ALPHATEC SPINE, INC.·Product code NKB·April 30, 2025

    ASR UNI FEMORAL IMPL SIZE 51

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·June 21, 2013

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·July 27, 2011

    PROLIEVE THERMODILITATION KIT

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MEQ·September 25, 2008