BEUDAMED
    8 results · 27ms · Sources: EU EUDAMED, US FDA

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    ARTEMA AQUA+ T & TS

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04047872673204·LEVAMED STABILI-TRI ANKLE SUP BLU R IV

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 14, 2024

    VEIN-GOGH INSTRUMENT

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    CONTOUR MENISCUS ARROW, MODELS 541110, 541113, AND 541116

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SORIN CENTRIFUGAL PUMP 5 (CP5)

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·June 27, 2014

    PENUMBRA SYSTEM REPERFUSION CATHETER 054

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·January 11, 2013

    PHOENIX ANTEGRADE FEMORAL NAIL SYSTEM

    FDA Adverse Event
    Malfunction ·EBI, LLC·Product code HSB·December 2, 2010