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

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    FINGER EXTENSION SPLINT

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    CADENCE PEEK CEMEENT RESTRICTOR

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

    CIRCUFLOW 5208 SEQUENTIAL COMPRESSION DEVICE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·May 21, 2014

    HS HAND CONTROLLED CURVED SHEA

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code GEI·November 16, 2007

    3.7MM TI CERVICAL SPINE SCREW SLF-DRLG/VARIABLE ANG

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code OVE·October 10, 2012