BEUDAMED
    8,651 results · 37ms · Sources: EU EUDAMED, US FDA

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    LED Light Therapy Mask (K9C-TK, K9C-K, K9P-YK, K9P-K, FM-03BK, FM-09K)

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    AFFINITY CP CENTRIFUGAL PUMP

    FDA Adverse Event
    Injury ·PERFUSION SYSTEMS·Product code KFM·November 15, 2019

    CUSTOM PERFUSION SYSTEM

    FDA Adverse Event
    Death ·MEDTRONIC·Product code KFM·December 19, 2016

    BULK NON STER XCOAT DELPH PUMP

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code KFM·October 21, 2016

    CENTRIFUGAL PUMP HEADS

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code KFM·November 8, 2016

    CENTRIFUGAL PUMP HEADS

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code KFM·November 3, 2016

    CENTRIFUGAL PUMP HEADS

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code KFM·November 4, 2016

    BULK NON STER XCOAT DELPH PUMP

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code KFM·November 17, 2016

    BULK NON STER XCOAT DELPH PUMP

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code KFM·August 6, 2015

    BULK NON STER XCOAT DELPH PUMP

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code KFM·September 3, 2015

    THORATEC CENTRIMAG

    FDA Adverse Event
    Death ·THORATEC SWITZERLAND GMBH·Product code KFM·August 27, 2015

    ROTAFLOW CENTRIFUGAL PUMP SYSTEM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code KFM·July 22, 2015

    BULK NON STER XCOAT DELPH PUMP

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code KFM·September 3, 2015

    ROTAFLOW CENTRIFUGAL PUMP SYSTEM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code KFM·July 22, 2015

    ROTAFLOW CENTRIFUGAL PUMP SYSTEM

    FDA Adverse Event
    Injury ·MAQUET CARDIOPULMONARY AG·Product code KFM·July 1, 2015

    ROTAFLOW CENTRIFUGAL PUMP SYSTEM

    FDA Adverse Event
    Injury ·MAQUET CARDIOPULMONARY AG·Product code KFM·July 15, 2015

    BULK NON STER XCOAT DELPH PUMP

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code KFM·July 6, 2015

    OVERPRESSURE SAFETY VALVE

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code KFM·July 22, 2015

    SINGLE STERILE XCOATED DELPHIN

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code KFM·August 6, 2015

    ROTAFLOW CENTRIFUGAL PUMP SYSTEM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY AG·Product code KFM·July 22, 2015