BEUDAMED
    9 results · 17ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    ENDOCLAMP AORTIC CATHETER

    FDA Adverse Event
    Injury ·HEARTPORT INC.·Product code DWF·August 30, 2001

    ENDOCLAMP AORTIC CATHETER

    FDA Adverse Event
    Injury ·HEARTPORT INC.·Product code DWF·August 30, 2001

    ENDOCLAMP AORTIC CATHETER

    FDA Adverse Event
    Injury ·HEARTPORT INC.·Product code DWF·August 30, 2001

    ENDOCLAMP AORTIC CATHETER

    FDA Adverse Event
    Injury ·HEARTPORT INC.·Product code DWF·August 30, 2001

    FEMUR SCREW STD 18MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code OLO·May 31, 2022

    UNKNOWN INTELLIJOINT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code OLO·May 31, 2022

    ARCOS CON SZ A STD 50MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·May 26, 2023

    ARCOS 15X190MM SPL TPR DIST

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·May 26, 2023

    28MM DIA COCR MOD HD -3MM NK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDG·May 26, 2023