BEUDAMED
    12 results · 22ms · Sources: EU EUDAMED, US FDA

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    CUI MAMMARY PROTHESIS SIZER

    FDA 510(k)
    FDA Unclassified ·Unknown

    SYNDEO PCA SYRINGE PUMP, MODEL 2L3113

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ARIX HAND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FLOEY CATHETER W TEMP

    FDA Adverse Event
    Injury ·DEGANIA SILICONE LTD·Product code DRF·October 17, 2017

    FOLEY CATHETER W TEMP

    FDA Adverse Event
    Malfunction ·DEGANIA SILICONE LTD.·Product code DRF·August 10, 2017

    FOLEY CATHETER W TEMP

    FDA Adverse Event
    Malfunction ·DEGANIA SILICONE LTD.·Product code DRF·August 10, 2017

    FOLEY CATHETER W TEMP

    FDA Adverse Event
    Malfunction ·DEGANIA SILICONE LTD.·Product code KOD·July 7, 2017

    TEMPORARY FIXATION PIN

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code FZX·May 25, 2014

    CHARGING SYSTEM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·November 5, 2012

    SIMILE

    FDA Adverse Event
    Injury ·PENTRON CLINICAL·Product code EBF·September 10, 2010

    FOLEY CATHETER W TEMP

    FDA Adverse Event
    Malfunction ·MMJ SA DE CV (USD)·Product code DRF·November 9, 2018

    SYNDEO SYRINGE PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code MEA·October 8, 2009