BEUDAMED
    12 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    UNK - SCREWS: TRAUMA

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HWC·January 9, 2023

    STREAK

    FDA Adverse Event
    Injury ·ADVANCED CARDIOVASCULAR SYSTEMS, INC.·Product code LOX·September 16, 1994

    TRECK CATHETER 4.0

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code LOX·November 12, 2014

    NC TRECK 4.5

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code LOX·November 5, 2014

    ACS RX STREAK 0.014

    FDA Adverse Event
    Injury ·ADVANCED CARDIOVASCULAR SYSTEMS·September 22, 1992

    ACS RX STREAK .010 CATHETR DILATATION CATHETER

    FDA Adverse Event
    Injury ·ACS, INC.·Product code DSP·September 15, 1992

    UNKNOWN TIBIAL TRAY

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 11, 2025

    UNKNOWN PERSONA FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 6, 2025

    UNKNOWN ARTICULAR SURFACE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 11, 2025

    UNKNOWN PERSONA TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 6, 2025

    UNKNOWN FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 11, 2025

    UNKNOWN PERSONA ARTICULAR SURFACE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 6, 2025