BEUDAMED
    6 results · 19ms · 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 Regulation: Us FDA ×

    TRIPLE LUMEN INFUSIONCATHETERS-

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    DROP FOOT BRACE

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    CYTOMEGELISA STAT

    FDA 510(k)
    FDA Class 2 ·Microbiology

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code LZS·May 2, 2014

    ULTRACISION DISSECT HOOK 10CM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC (CINCINNATI)·Product code LFL·December 14, 2007

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·November 15, 2012