BEUDAMED
    106 results · 29ms · Sources: EU EUDAMED, US FDA

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    CARDIO MESSENGER LLT

    FDA Adverse Event
    Malfunction ·BIOTRONIK GMBH AND CO.·Product code DSI·February 2, 2007

    FETAL MONITOR

    FDA Adverse Event
    Malfunction ·HEWLETT PACKARD·Product code LLT·January 22, 1993

    MICROBORE EXTENSION SET W/LL T-CONNECTOR

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code FPA·February 5, 2002

    MICROBORE EXTENSION SET W/LL T-CONNECTOR

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code FPA·December 22, 2000

    DGW .035 FC STR 150CM TEF LLT

    FDA Adverse Event
    Malfunction ·LAKE REGION·Product code DQX·January 30, 2017

    MICROBORE EXTENSION SET W/LL T-CONNECTOR

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code FPA·November 23, 2001

    MICROBORE EXTENSION SET W/LL T-CONNECTOR

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code FPA·November 23, 2001

    MICROBORE EXTENSION SET W/LL T-CONNECTOR

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code FPA·March 15, 2001

    MICROBORE EXTENSION SET W/LL T-CONNECTOR

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code FPA·June 30, 2003

    NEUMANN TI ARTHR PLT PROX L LT

    FDA Adverse Event
    Malfunction ·NORMED MEDIZIN-TECHNIK GMBH·Product code HRS·March 20, 2015

    MICROBORE EXTENSION SET W/LL T-CONNECTOR

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code FPA·April 30, 2001

    MICROBORE EXTENSION SET W/LL T-CONNECTOR

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code FPA·April 19, 2002

    MICROBORE EXTENSION SET W/LL T-CONNECTOR

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code FPA·December 16, 2002

    MICROBORE EXTENSION SET W/LL T-CONNECTOR

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code FPA·November 13, 2002

    T- COATED HEAVY DUTY NEWTON LLT WIRE GUIDE

    FDA Adverse Event
    Malfunction ·COOK, INC.·Product code DQX·April 17, 2007

    DURA MOD FEM N/BEAD M/L LT

    FDA Adverse Event
    Malfunction ·HOWMEDICA INC.·Product code HSA·December 11, 1997

    MAXON

    FDA Adverse Event
    Malfunction ·DAVIS & GECK CARIBE LTD·Product code GAM·November 3, 2025

    ESSURE

    FDA Adverse Event
    Malfunction ·BAYER PHARMA AG·Product code HHS·August 7, 2014

    ESSURE

    FDA Adverse Event
    Malfunction ·BAYER PHARMA AG·Product code HHS·February 16, 2017

    ESSURE

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE LLC·Product code HHS·October 13, 2016