BEUDAMED
    3 results · 20ms · 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 FDA Adverse Event ×

    5.0MM FLEXIBLE SHAFT

    FDA Adverse Event
    Malfunction ·SYNTHES BETTLACH·Product code HTO·May 21, 2014

    AGILIS NXT, 8.5F, STEERABLE INTRODUCER, SMALL CURL

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL·Product code DYB·July 17, 2008

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Malfunction ·WAVELIGHT GMBH·Product code LZS·August 27, 2010