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

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    STANDARD NEBULIZER HEATER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ILLUMINATOR VII MINI/LUM LIGHT

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SUTURE REMOVAL KIT, STERILE, DISPOSABLE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES·Product code MIH·January 18, 2013

    RESTORE RECHARGEABLE NEUROSTIMULATOR

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·November 11, 2010

    ISOFLEX S

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 10, 2014