BEUDAMED
    33 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Death ×

    SINGLE TUBE HOSE, 90496/91496/91

    FDA Adverse Event
    Death ·SPACELABS HEALTHCARE, INC.·Product code DXG·October 18, 2018

    CENTRAL VENOUS CATHETER

    FDA Adverse Event
    Death ·UNKNOWN·Product code DXG·June 11, 1993

    GROSHONG CATHETER (CENTRAL VENOUS)

    FDA Adverse Event
    Death ·UNKNOWN·Product code DXG·June 11, 1993

    ARROWGARD

    FDA Adverse Event
    Death ·ARROW-HOWES·Product code DXG·April 27, 1993

    M3155B INFO CTR NETWORK DB

    FDA Adverse Event
    Death ·PHILIPS MEDICAL SYSTEMS·Product code DXG·April 3, 2006

    ARROW HOWES MULTI LUMEN CENTRAL VENOUS CATHETER KIT

    FDA Adverse Event
    Death ·ARROW HOWES·Product code DXG·March 5, 1992

    VIGILEO MONITOR

    FDA Adverse Event
    Death ·EDWARDS LIFESCIENCES·Product code DXG·November 20, 2012

    ARROW HOWES

    FDA Adverse Event
    Death ·ARROW INTERNATIONAL, INC.·Product code DXG·November 17, 1992

    ARROWGARD

    FDA Adverse Event
    Death ·ARROW-HOWES·Product code DXG·September 20, 1993

    GROSHONG CATHETER (CENTRAL VENOUS)

    FDA Adverse Event
    Death ·UNKNOWN·Product code DXG·July 13, 1993

    COOK CENTRAL VENOUS CATHETER TRAY

    FDA Adverse Event
    Death ·COOK INCORPORATED·Product code DXG·July 17, 1992

    PER-Q-CATH

    FDA Adverse Event
    Death ·GESCO INTERNATIONAL, INC.·Product code DXG·July 30, 1992

    COOK CENTRAL VENOUS CATHETER TRAY

    FDA Adverse Event
    Death ·COOK INCORPORATED·Product code DXG·July 2, 1992

    MAHURKAR-DUAL LUMEN CATHETER

    FDA Adverse Event
    Death ·QUINTON INSTRUMENT CO.·Product code DXG·August 18, 1992

    PER-Q-CATH

    FDA Adverse Event
    Death ·GESCO INTERNATIONAL, INC.·Product code DXG·July 30, 1992

    MAHURKAR - DUAL LUMEN CATHETER

    FDA Adverse Event
    Death ·QUINTON INTRUMENT CO.·Product code DXG·August 18, 1992

    ACCOLADE (127 DEG) SIZE 2.5

    FDA Adverse Event
    Death ·STRYKER ORTHOPAEDICS CORK·Product code MEH·December 18, 2012

    ACCOLADE (127 DEG) SIZE 4.5

    FDA Adverse Event
    Death ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·March 14, 2017

    SIZE 3 ACCOLADE II 127 DEG

    FDA Adverse Event
    Death ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·May 10, 2021

    HFN LH 130 DEG 11MM X 340MM

    FDA Adverse Event
    Death ·BIOMET TRAUMA·Product code HSB·March 9, 2016