BEUDAMED
    21 results · 76ms · Sources: EU EUDAMED, US FDA

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    CENTRYSYSTEM

    FDA Adverse Event
    Injury ·COBE RENAL CARE, INC.·Product code FII·April 18, 1996

    CENTRYSYSTEM

    FDA Adverse Event
    Injury ·COBE RENAL CARE, INC.·Product code FII·April 18, 1996

    CENTURY 3

    FDA Adverse Event
    COBE RENAL CARE, INC.·Product code FII·May 24, 1996

    CENTRYSYSTEM

    FDA Adverse Event
    Injury ·COBE RENAL CARE, INC.·Product code FII·April 18, 1996

    BLOOD TUBING

    FDA Adverse Event
    Injury ·COBE RENAL CARE, INC.·Product code FJK·March 3, 1995

    RENALYTE

    FDA Adverse Event
    COBE RENAL CARE, INC.·Product code KPO·January 5, 1995

    COBE C3

    FDA Adverse Event
    Injury ·COBE RENAL CARE, INC.·Product code FII·December 13, 1996

    CENTRYSYSTEM HG400

    FDA Adverse Event
    Injury ·COBE RENAL CARE, INC.·Product code FJI·April 21, 1995

    CENTRY SYSTEM HG 400

    FDA Adverse Event
    Injury ·COBE RENAL CARE, INC.·Product code FJI·May 1, 1995

    CENTRY SYSTEM BLOOD TUBING

    FDA Adverse Event
    Malfunction ·COBE RENAL CARE, INC.·Product code FJK·June 20, 1995

    GAMBRO LUNDIA, ALPHA 500 PLATE DIALYZER

    FDA Adverse Event
    Malfunction ·COBE RENAL CARE, INC.·Product code FJG·October 31, 1995

    ALPHA DIALYZER

    FDA Adverse Event
    Injury ·COBE RENAL CARE, INC.·Product code FJG·December 21, 1995

    RENALYTE RX CA-2.50

    FDA Adverse Event
    COBE RENAL CARE, INC.·Product code KPO·October 5, 1995

    RENALYTE RX

    FDA Adverse Event
    COBE RENAL CARE, INC.·Product code KPO·October 5, 1995

    RENALYTE RX CA-FREE

    FDA Adverse Event
    COBE RENAL CARE, INC.·Product code KPO·October 5, 1995

    COBE CENTRYSYSTEM 3W

    FDA Adverse Event
    Injury ·COBE RENAL CARE, INC.·Product code FII·February 26, 1997

    COBE CENTRYSYSTEM 3W

    FDA Adverse Event
    Injury ·COBE RENAL CARE, INC.·Product code FII·February 27, 1997

    CARTRIDGE

    FDA Adverse Event
    Injury ·COBE RENAL CARE, INC.·Product code FJK·January 9, 1998

    COBE CENTRY 3

    FDA Adverse Event
    Injury ·COBE RENAL CARE INC.·Product code FII·January 9, 1998

    COBE CARTRIDGE

    FDA Adverse Event
    Malfunction ·COBE RENAL CARE, INC.·Product code FJI·January 10, 1996