BEUDAMED
    232 results · 56ms · Sources: EU EUDAMED, US FDA

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    THERMOCOOL® SMART TOUCH¿ BI-DIRECTIONAL NAVIGATION CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·March 12, 2024

    UNK_QDOT MICRO

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code OAE·March 18, 2024

    THERMOCOOL® SMART TOUCH® SF BI-DIRECTIONAL NAVIGATION CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·March 15, 2024

    UNKNOWN - UNPSECIFIED

    FDA Adverse Event
    Injury ·COOK BIOTECH, INC.·Product code FTM·August 14, 2014

    GORE® TAG® THORACIC ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·October 11, 2023

    UNK - UNSPECIFIED

    FDA Adverse Event
    Injury ·COOK BIOTECH, INC.·Product code FTL·August 14, 2014

    UNKNOWN - UNSPECIFIED

    FDA Adverse Event
    Injury ·COOK BIOTECH, INC.·Product code FTM·August 14, 2014

    UNKNOWN - UNSPECIFIED

    FDA Adverse Event
    Injury ·COOK BIOTECH, INC.·Product code FTM·August 14, 2014

    UNKNOWN - UNSPECIFIED

    FDA Adverse Event
    Injury ·COOK BIOTECH, INC.·Product code FTM·August 14, 2014

    UNKNOWN - UNSPECIFIED

    FDA Adverse Event
    Injury ·COOK BIOTECH, INC.·Product code FTM·August 14, 2014

    UNKNOWN - UNSPECIFIED

    FDA Adverse Event
    Injury ·COOK BIOTECH, INC.·Product code FTM·August 14, 2014

    UNKNOWN - UNSPECIFIED

    FDA Adverse Event
    Injury ·COOK BIOTECH, INC.·Product code PAG·August 14, 2014

    UNKNOWN - UNSPECIFIED

    FDA Adverse Event
    Injury ·COOK BIOTECH, INC.·Product code FTM·August 14, 2014

    UNKNOWN - UNSPECIFIED

    FDA Adverse Event
    Injury ·COOK BIOTECH, INC.·Product code FTM·August 14, 2014

    GUIDESTAR STEERABLE GUIDING SHEATH

    FDA Adverse Event
    Injury ·OSCOR INC.·Product code DYB·November 6, 2020

    MICROCUFF ADULT ENDOTRACHEAL TUBE

    FDA Adverse Event
    Malfunction ·AVANOS MEDICAL INC.·Product code BTR·January 18, 2024

    CARTO VIZIGO 8.5F BI-DIRECTIONAL GUIDING SHEATH - MEDIUM

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code DYB·June 8, 2021

    UNICEL DXC 800 SYNCHRON SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·August 19, 2011

    UNICEL DXC 800 SYNCHRON SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·September 30, 2011

    UNKNOWN - UNSPECIFIED

    FDA Adverse Event
    Injury ·COOK BIOTECH, INC.·Product code FTM·August 14, 2014