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

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    Filters Regulation: Us FDA ×

    DERMAGRIP POWDER FREE LATEX EXAMINATION GLOVE, NON STERILE (PROTEIN CONTENT LABELING)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SPINAL USA ANTERIOR LUMBAR PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TRACHEOSTOMY TUBES, SHORT AND LONG TERM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SLIMLINE OPERATIVE HYSTEROSCOPE INNER SHEATH/BRIDGE

    FDA Adverse Event
    Malfunction ·GYRUS ACMI, INC·Product code FAS·February 9, 2021

    PROGRAMMING SOFTWARE

    FDA Adverse Event
    Malfunction ·CYBERONICS INC·Product code LYJ·March 6, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 15, 2011

    CAPSURE SP

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 2014

    AMPLATZER AMULET

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code NGV·May 28, 2024