BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    COLLECT.NO.QAS KNEE IMPLANTS ROTAT.HINGE

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·May 12, 2021

    530G INSULIN PUMP

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

    COLLEAGUE

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

    OCTRODE

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

    COLLECT.NO.QAS KNEE IMPLANTS ROTAT.HINGE

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code KRO·December 1, 2021

    AS ENDURO FEMORAL COMPONENT CEMENTED F1R

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·September 1, 2021

    ENDURO MENISCAL COMPONENT F3 10MM

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code KRO·August 4, 2021

    COLLECT.NO.QAS KNEE IMPLANTS ROTAT.HINGE

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code HRZ·August 10, 2022