BEUDAMED
    11 results · 28ms · Sources: EU EUDAMED, US FDA

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    REAGENT CUPS

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    DATASCOPE CA 40 8FR. IABS, MODEL 0684-00-04XX

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PG-800A SERIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    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

    RESTORE ADVANCED

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·November 14, 2012

    KIMVENT READY CARE ORAL CARE SUCTION PROBE

    FDA Adverse Event
    Malfunction ·Product code KXF·September 10, 2010

    FOLEY CATHETER W TEMP

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