BEUDAMED
    11 results · 30ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

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    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·March 14, 2018

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 10, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 4, 2014

    NEXGEN STEMMED TIBIAL COMPONENT

    FDA Adverse Event
    Malfunction ·ZIMMER INC·Product code HSH·November 24, 2010

    PS TIBIAL INSERTS SZ 4, 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·April 14, 2023

    CC FEMORAL SZ 3

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 10, 2024

    CEMENTED FINNED TIB. TRA SZ 3F/3T

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·December 19, 2024

    OPTETRAK KNEE SYSTEM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·July 23, 2024

    OPTETRAK KNEE COMPONENTS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 29, 2024

    PS TIBIAL INSERTS SZ 2, 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·January 13, 2025

    CC TIBIAL INSERT SZ 4, 11MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 4, 2024