BEUDAMED
    825 results · 42ms · Sources: EU EUDAMED, US FDA

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    DATASCOPE CORPORATION

    FDA Adverse Event
    Injury ·DATASCOPE CORPORATION·Product code DSP·February 21, 2002

    DATASCOPE CORPORATION

    FDA Adverse Event
    Malfunction ·DATA SCOPE CORP. CARDIAC ASSIST DIV.·Product code DSP·October 8, 1999

    MAQUET (DATASCOPE CORPORATION)

    FDA Adverse Event
    Injury ·MAQUET·Product code DSP·February 12, 2015

    CLEARGLIDE PRECIS BIPOLAR

    FDA Adverse Event
    Malfunction ·DATASCOPE CORPORATION·Product code GEI·June 26, 2009

    CLEARGLIDE EVH SMALL

    FDA Adverse Event
    Malfunction ·EVH·Product code GEI·June 29, 2009

    CLEARGLIDE EVH SMALL

    FDA Adverse Event
    Malfunction ·DATASCOPE CORPORATION·Product code GEI·June 25, 2009

    INTRA-AORTIC BALLOON CATHETER

    FDA Adverse Event
    Injury ·DATASCOPE CORP.·Product code DSP·July 25, 1997

    SPECTRUM

    FDA Adverse Event
    Death ·DATASCOPE CORP.·Product code MHX·September 29, 2006

    PERCOR STAT DL 9.5 FR. 40 CC IAB

    FDA Adverse Event
    Injury ·DATASCOPE CORP.·Product code DSP·July 25, 1997

    PERCOR STAT DL 9.5 FR. 40 CC IAB

    FDA Adverse Event
    Injury ·DATASCOPE CORP.·Product code DSP·July 25, 1997

    CLEARGLIDE PRECIS BIPOLAR

    FDA Adverse Event
    Malfunction ·DATASCOPE CORPORATION·Product code GEI·July 31, 2009

    PERCOR STAT DL 9.5 FR. 40 CC IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·July 25, 1997

    STAT DL 9.5 FR. 40CC. IAB

    FDA Adverse Event
    Death ·DATASCOPE CORP.·Product code DSP·August 1, 1998

    DATASCOPE

    FDA Adverse Event
    Injury ·DATASCOPE CORP.·Product code DSP·July 29, 1997

    INTRA-AORTIC BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·DATASCOPE CORPORATION·Product code DSP·July 25, 1997

    PERCOR STAT DL 9.5 FR 40 CC IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·September 9, 1997

    PERCOR STAT DL 9.5 FR. 40 CC IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORPORATION·Product code DSP·July 25, 1997

    CLEARGLIDE PRECISION BIPOLAR

    FDA Adverse Event
    Malfunction ·DATASCOPE CORPORATION·Product code GEI·November 3, 2009

    INTRA-AORTIC BALLOON CATHETER

    FDA Adverse Event
    DATASCOPE CORPORATION·Product code DSP·October 28, 1997

    Low-Level Output Cable. The device is used to allow the information displayed on the Intra-aortic balloon pump (IABP) to be displayed on a separate patient monitor.

    FDA Recall
    Terminated ·Datascope Corporation·Product code DSP·February 4, 2009