BEUDAMED
    6 results · 19ms · Sources: EU EUDAMED, US FDA

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    BRINK PRE-MAXILLARY IMPLANT

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

    SURELASE CO2 LASER SYSTEM

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

    OPTILOCK IMPLANTABLE ACCESS PORT, MODELS #1700-01, 1700-02, 1700-03, 1700-04 AND 1700-05

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SCREW

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HWC·January 18, 2013

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 6, 2014

    ATTAIN ABILITY

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code OJX·December 13, 2010