BEUDAMED
    4 results · 32ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    OPTETRAK KNEE COMPONENT - TIBIAL INSERT

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

    5MM, 33CM PEEK MONOPOLAR HANDLE 33CM

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY-SAN JOSE·Product code KOG·June 2, 2014

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·November 21, 2012

    TERUMO CDI 540 CALIBRATOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·August 31, 2010