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

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    LM-90 ESU

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    N Series Patient Monitors

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LANDMARK VENOUS ACCESS DEVICE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ENDOTAK RELIANCE G

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code LWS·January 14, 2013

    CORE IMPACTION DRILL

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code DZJ·November 26, 2010

    SOFTCLIX ® PLUS GT LANCET DEVICE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·July 3, 2014