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

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    TISSUE EXPANDER

    FDA 510(k)
    FDA Unclassified ·Unknown

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172971819·

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172971796·

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172971802·

    STERILUCENT PSD-85 HYDROGEN PEROXIDE STERILIZER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    AMEDICA DRUG SCREEN THC/COC, OP1300, PPX, OXY, BAR/BZO TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    OPERATING CYSTOSCOPE-URETHROSCOPE

    FDA Adverse Event
    Death ·KARL STORZ SE & CO. KG·Product code FGB·March 8, 2023

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·May 30, 2014

    PROMUS ELEMENT ¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·November 20, 2012

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    FDA Adverse Event
    Malfunction ·THERAKOS·Product code LNR·September 8, 2010