BEUDAMED
    11 results · 36ms · Sources: EU EUDAMED, US FDA

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    RELIANCE TEMPO OPHTH. INSTR STAND

    FDA 510(k)
    FDA Class 1 ·Obstetrics/Gynecology

    BICONITE SURFACE TREATMENT

    FDA 510(k)
    FDA Class 2 ·Dental

    SUDO PATH

    FDA 510(k)
    FDA Class 2 ·Neurology

    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

    HEARTWARE® VENTRICULAR ASSIST SYSTEM

    FDA Adverse Event
    Malfunction ·HEARTWARE, INC·Product code DSQ·May 25, 2014

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·November 14, 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