BEUDAMED
    146 results · 71ms · Sources: EU EUDAMED, US FDA

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    L-CATH PERIPHERALLY INSERTED VENOUS CATH

    FDA Adverse Event
    Other ·LUTHER MEDICAL PRODUCTS·Product code DQO·August 15, 1997

    L-CATH PEEL AWAY

    FDA Adverse Event
    Injury ·LUTHER MEDICAL PRODUCTS, INC.·Product code FOZ·September 24, 1996

    L CATH PEAL AWAY SYSTEM (DUAL CATH)

    FDA Adverse Event
    Death ·LUTHER MEDICAL PRODUCTS, INC.·Product code FOS·September 6, 1996

    PERIPHERALLY INSERTED CENTRAL CATHETER

    FDA Adverse Event
    Malfunction ·LUTHER MEDICAL PRODUCTS, INC.·Product code DQO·September 4, 1996

    LUTHER L-CATH

    FDA Adverse Event
    Malfunction ·LUTHER MEDICAL PRODUCTS, INC.·Product code DQO·January 4, 2002

    L-CATH PEEL AWAY PICC

    FDA Adverse Event
    Injury ·LUTHER MEDICAL PRODUCTS, INC.·Product code DQO·April 10, 1996

    L-CATHETER

    FDA Adverse Event
    Injury ·LUTHER MEDICAL PRODUCTS, INC.·Product code DQO·May 9, 1996

    LUTHER L-CATH

    FDA Adverse Event
    Malfunction ·LUTHER MEDICAL PRODUCTS, INC.·Product code DQO·July 11, 2003

    L-CATH

    FDA Adverse Event
    Malfunction ·LUTHER MEDICAL PRODUCTS, INC.·Product code DQO·March 17, 1994

    L-CATH

    FDA Adverse Event
    Other ·LUTHER MEDICAL PRODUCTS, INC.·Product code DQO·February 7, 1994

    L-CATH

    FDA Adverse Event
    Malfunction ·LUTHER MEDICAL PRODUCTS, INC.·Product code DQO·February 17, 1994

    L-CATH PEEL AWAY

    FDA Adverse Event
    Malfunction ·LUTHER MEDICAL PRODUCTS, INC.·Product code DQO·March 17, 1994

    PICC CATHETER

    FDA Adverse Event
    Injury ·LUTHER MEDICAL PRODUCTS, INC.·Product code DQO·June 7, 1999

    L CATH INTRODUCER

    FDA Adverse Event
    Malfunction ·LUTHER MEDICAL PRODUCTS, INC.·Product code DYB·May 14, 1999

    L-CATH MIDLINE

    FDA Adverse Event
    Injury ·LUTHER MEDICAL PRODUCTS, INC.·Product code DQO·April 21, 1999

    PICC CATHETER

    FDA Adverse Event
    Injury ·LUTHER MEDICAL PRODUCTS, INC.·Product code DQO·June 7, 1999

    L CATH INTRODUCER

    FDA Adverse Event
    Malfunction ·LUTHER MEDICAL PRODUCTS, INC.·Product code DYB·June 10, 1999

    L CATH CATHETER SYSTEM

    FDA Adverse Event
    Injury ·LUTHER MEDICAL PRODUCTS, INC.·Product code DQO·June 17, 1999

    L CATH INTRODUCER

    FDA Adverse Event
    Malfunction ·LUTHER MEDICAL PRODUCTS, INC.·Product code DYB·May 14, 1999

    L CATH CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·LUTHER MEDICAL PRODUCTS, INC.·Product code DQO·June 1, 1999