BEUDAMED
    9 results · 50ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    BENCOX HIP SYSTEM

    FDA Adverse Event
    Injury ·CORENTEC CO.,LTD.·Product code LPH·November 8, 2020

    CORENTEC LOSPA SIZE 6-KNEE PROSTHESIS

    FDA Adverse Event
    Injury ·CORENTEC CO., LTD.·Product code JWH·September 5, 2023

    LOSPA KNEE SYSTEM

    FDA Adverse Event
    Injury ·CORENTEC CO., LTD.·Product code JWH·September 11, 2018

    BENCOX TOTAL HIP SYSTEM

    FDA Adverse Event
    Malfunction ·CORENTEC CO.,LTD.·Product code LPH·November 9, 2023

    BENCOX TOTAL HIP SYSTEM INSTRUMENT HEAD TRIAL

    FDA Adverse Event
    Malfunction ·CORENTEC CO., LTD.·Product code KWY·September 11, 2018

    LOSPA KNEE SYSTEM OR EXULT KNEE SYSTEM

    FDA Adverse Event
    Injury ·CORENTEC CO.,LTD.·Product code JWH·October 16, 2023

    LOSPA TOTAL KNEE REPLACMENT SYSTEM

    FDA Adverse Event
    Injury ·CORENTEC CO., LTD.·Product code JWH·June 1, 2016

    BENCOX PE LINER 36/44

    FDA Adverse Event
    Injury ·CORENTEC CO., LTD.·Product code LPH·June 23, 2016

    CORENTEC HIP REPLACEMENT

    FDA Adverse Event
    Injury ·CORENTEC CO., LTD.·Product code KWA·September 11, 2019