BEUDAMED
    12 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    COLLECT.NO.QAS KNEE IMPLANTS COLUMBUS

    FDA Adverse Event
    Malfunction ·AESCULAP IMPLANT SYSTEMS·Product code KRO·November 21, 2017

    AE-QAS-K521-53

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·December 19, 2024

    AS COLUMBUS REV F TIB.OFFSET CEMENT.T2+

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·March 20, 2023

    AS COLUMBUS REV F FEMUR CEMENTED F4L

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·March 20, 2023

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 16, 2011

    530G INSULIN PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·November 14, 2014

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·July 25, 2013

    COLLECT.NO.QAS KNEE IMPLANTS COLUMBUS

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·June 22, 2021

    COLLECT.NO.QAS KNEE IMPLANTS COLUMBUS

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·June 22, 2021

    COLUMBUS

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code OOG·December 1, 2023

    COLLECT.NO.QAS KNEE IMPL.MISC./UNKNOWN

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·March 5, 2021

    COLUMBUS

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code OOG·December 1, 2023