BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    HARBOR Occlusion Device

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Mediflex Laparoscopic Instruments - Reusable Electrodes

    FDA UDI
    FLEXBAR MACHINE CORPORATION·00842102104930·J Hook Cautery 3.5mm x 33cm

    ONE TOUCH ULTRA

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·July 30, 2002

    PROFEMUR Preserve Size 1-3 Hip Stems

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    D-STAT RADIAL HEMOSTATIC BAND

    FDA 510(k)
    FDA Unclassified ·Unknown

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·November 14, 2014

    SPYGLASS DIRECT VISUALIZATION SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code KOG·September 15, 2011

    ANIMAS INSULIN CARTRIDGE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 26, 2013

    CURRENT HEALTH MONITORING SYSTEM GEN 2 (G2)

    FDA Adverse Event
    Death ·CURRENT HEALTH LTD·Product code MSX·September 9, 2024