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

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    ACE CANCELLOUS BONE SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ATRAMAT PGLA90 POLY(GLYCOLIDE-CO-L-LACTIDE) SURGICAL SUTURES

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

    Prosomnus [CA] Sleep and Snore Device and Prosomnus [CA] Sleep and Snore Device with Micro-recorder

    FDA 510(k)
    FDA Class 2 ·Dental

    MINICAP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·June 13, 2014

    SAVVY PTA DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·CORDIS EUROPA, N.V.·Product code LIT·October 18, 2010

    APEX¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LOX·December 13, 2012