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

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    MULTICHECK(TM)

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776362386·Bunnell Tendon Passer,

    ZOETIC GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ALPHA SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AMPLATZER CRIBRIFORM OCCLUDER

    FDA Adverse Event
    Injury ·AGA MEDICAL CORPORATION·Product code MLV·March 20, 2020

    ECLIPSE FILTER SYSTEM - FEMORAL

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·December 16, 2010

    MEGA SUTURECUT NEEDLE DRIVER INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·July 15, 2014

    COMPLY

    FDA Adverse Event
    Malfunction ·3M HEALTHCARE·Product code FLE·November 27, 2012