BEUDAMED
    3 results · 16ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Status: Injury ×

    IRIDEX MICROPULSE P3 PROBE

    FDA Adverse Event
    Injury ·IRIDEX CORP.·Product code GEX·July 27, 2022

    PINNACLE MTL INS NEUT28IDX50OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·June 12, 2014

    UNKNOWN STRYKER LEFT KNEE

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code JDI·December 4, 2012