BEUDAMED
    343 results · 45ms · Sources: EU EUDAMED, US FDA

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    MAHURKAR DUAL LUMEN CATHETER

    FDA Adverse Event
    Malfunction ·Product code LFJ·June 12, 1997

    ANGIO-SEAL

    FDA Adverse Event
    Injury ·SHERWOOD MEDICAL INDUSTRIES OF IRELAND, LTD.·Product code MGB·March 14, 1997

    ANGIO-SEAL

    FDA Adverse Event
    Injury ·SHERWOOD MEDICAL INDUSTRIES OF IRELAND, LTD.·Product code MGB·January 10, 1997

    QUINTON INSTRUMENT CO.

    FDA Adverse Event
    Malfunction ·QUINTON INSTRUMENT CO.·Product code DYB·February 20, 1998

    ANGIO-SEAL

    FDA Adverse Event
    Injury ·SHERWOOD MEDICAL INDUSTRIES OF IRELAND, LTD.·Product code MGB·March 14, 1997

    PERMCATH DUAL LUMEN DIALYSIS CATHETER

    FDA Adverse Event
    QUINTON INSTRUMENT CO.·Product code LFJ·July 8, 1996

    PERMCATH DUAL LUMEN

    FDA Adverse Event
    Malfunction ·QUINTON INSTRUMENT CO.·Product code LFJ·May 31, 1996

    MAHURKAR DIALYSIS CATHETER

    FDA Adverse Event
    Malfunction ·QUINTON INSTRUMENT CO.·Product code LFJ·March 18, 1994

    CURLED PERITONEAL CATHETER

    FDA Adverse Event
    Other ·QUINTON INSTRUMENT CO.·Product code FJS·February 10, 1994

    PERMACATH, 36 CM

    FDA Adverse Event
    Death ·QUINTON INSTRUMENT CO.·Product code LFJ·March 29, 1994

    QUINTON CATHETER

    FDA Adverse Event
    Injury ·QUINTON INSTRUMENT CO·Product code LFK·May 17, 2000

    PERMCATH

    FDA Adverse Event
    Injury ·QUINTON INSTRUMENT CO.·Product code LFJ·February 6, 1995

    PERMCATH

    FDA Adverse Event
    Injury ·QUINTON INSTRUMENT CO.·Product code LFJ·February 6, 1995

    ANGIO-SEAL

    FDA Adverse Event
    Injury ·QUINTON INSTRUMENT CO.·Product code MGB·August 28, 1997

    ANGIO-SEAL

    FDA Adverse Event
    Injury ·QUINTON INSTRUMENT CO.·Product code MGB·August 12, 1997

    ANGIO-SEAL

    FDA Adverse Event
    Injury ·QUINTON INSTRUMENT CO.·Product code MGB·September 17, 1997

    QUINTON CATHETER

    FDA Adverse Event
    Death ·QUINTON INSTRUMENT CO.·Product code MSD·July 31, 1997

    ANGIO-SEL

    FDA Adverse Event
    Malfunction ·QUINTON INSTRUMENT CO.·Product code MGB·August 22, 1997

    ANGIO-SEAL

    FDA Adverse Event
    Malfunction ·QUINTON INSTRUMENT CO.·Product code MGB·September 8, 1997

    ANGIO-SEAL

    FDA Adverse Event
    Injury ·QUINTON INSTRUMENT CO.·Product code MGB·September 12, 1997