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

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    EZ STEER NAVIGATIONAL 4MM

    FDA Adverse Event
    Death ·BIOSENSE WEBSTER, INC. (IRWINDALE)·Product code DRF·August 18, 2016

    EZ STEER NAVIGATIONAL 4MM (TC)

    FDA Adverse Event
    Death ·BIOSENSE WEBSTER, INC. (IRWINDALE)·Product code LPB·August 18, 2016

    BD® WHITACRE SPINAL NEEDLES SET

    FDA Adverse Event
    Injury ·BECTON DICKINSON, S.A.·Product code BSP·July 7, 2023

    MIC G-16 INTRODUCER KIT

    FDA Adverse Event
    Injury ·KIMBERLY-CLARK·Product code KDH·January 8, 2010

    ETHOX

    FDA Adverse Event
    Malfunction ·ETHOX LLC.·Product code KDH·December 13, 2017

    8FR REPLOGLE SUCT CATH

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code KDH·April 15, 2022

    SUCTION CATHETER

    FDA Adverse Event
    Malfunction ·MEDOVATIONS, INC.·Product code KDH·May 13, 1996

    RUSCH

    FDA Adverse Event
    Malfunction ·WILLY RUSCH GMBH·Product code KDH·November 4, 2003

    KIMBERLY CLARK EASI-LAV

    FDA Adverse Event
    Malfunction ·KIMBERLY CLARK·Product code KDH·August 26, 2003

    OLYMPUS

    FDA Adverse Event
    Injury ·NORTECH·Product code KDH·January 24, 1994

    OLYMPUS IRRIGATION ASPIRATOR

    FDA Adverse Event
    Injury ·OLYMMPUS AMERICA INC·Product code KDH·February 4, 1994

    TRIPLE-PORT GASTROSTOMY TUBE

    FDA Adverse Event
    Malfunction ·RUSCH, INC.·Product code KDH·June 15, 2000

    GILSDORF GASTROSTOMY CATHETER

    FDA Adverse Event
    Malfunction ·RUSCH, INC.·Product code KDH·June 15, 2000

    TRIPLE-PORT GASTROSTOMY TUBE

    FDA Adverse Event
    Injury ·RUSCH INC.·Product code KDH·April 5, 1999

    GILSDORF GASTROSTOMY CATHETER

    FDA Adverse Event
    Injury ·RUSCH, INC.·Product code KDH·May 19, 1999

    BLAKEMORE TUBE

    FDA Adverse Event
    Malfunction ·WILLY RUSCH AG·Product code KDH·January 24, 2003

    TRIPLE-PORT GASTROSTOMY TUBE

    FDA Adverse Event
    Malfunction ·RUSCH, INC.·Product code KDH·November 2, 2000

    *

    FDA Adverse Event
    Death ·*·Product code KDH·September 17, 2004

    *

    FDA Adverse Event
    Death ·*·Product code KDH·August 31, 2004

    BLAKEMORE TUBE

    FDA Adverse Event
    Injury ·RUSCH MFG. UK, LTD.·Product code KDH·April 18, 1997