BEUDAMED
    11 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    CHLORAPREP ONE STEP HI-LITE ORANGE

    FDA Adverse Event
    Malfunction ·CAREFUSION 213, LLC 0113·Product code KXG·August 3, 2021

    CHLORAPREP ONE STEP HI- LITE ORANGE

    FDA Adverse Event
    Malfunction ·CAREFUSION 213, LLC 0113·Product code KXG·May 18, 2021

    CHLORAPREP ONE STEP HI-LITE ORANGE

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code KXG·November 9, 2020

    CHLORAPREP ONE STEP HI-LITE ORANGE

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code KXG·December 27, 2020

    CHLORAPREP ONE-STEP HILITE ORANGE

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code KXG·August 17, 2021

    CHLORAPREP ONE-STEP HI LITE ORANGE

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code KXG·February 2, 2021

    TERUMO CDI 101 MONITOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTY·November 24, 2010

    GRANUFLO

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·January 23, 2013

    XIENCE PRIME EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIQ·July 11, 2014

    ACTIVA

    FDA Adverse Event
    Injury ·RICE CREEK MFG·Product code MHY·February 11, 2020

    ACTIVA

    FDA Adverse Event
    Malfunction ·RICE CREEK MFG·Product code MHY·February 11, 2020