BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Dynamic TiBase

    FDA 510(k)
    FDA Class 2 ·Dental

    Oticon

    FDA UDI
    Oticon A/S·05714464008612·AGXO F300 MINIRITE R C044

    Q LAB SOFTWARE

    FDA 510(k)
    FDA Class 2 ·Radiology

    7D Surgical FlashLock 1, 7D Surgical Flex Rod Connector - 5.5 mm - 150 mm, 7D Surgical Flex Array

    FDA 510(k)
    FDA Class 2 ·Neurology

    LONG NAIL KIT R1.5, TI, LEFT GAMMA3 10X320MM X 12

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·July 19, 2012

    ANGIOGUARD RX

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code NTE·November 3, 2008

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·August 24, 2011

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·July 5, 2013