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 ×

    ASTRAL 150 - DEU

    FDA Adverse Event
    Malfunction ·RESMED LTD·Product code NOU·July 10, 2015

    CONSTELLATION VISION SYS

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CTR·Product code HQC·February 26, 2014

    IAB : 8 FR - 40 CC FOS

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code DSP·November 5, 2010