BEUDAMED
    3 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 FDA Adverse Event ×

    HYPERFORM OCCLUSION BALLOON SYSTEM

    FDA Adverse Event
    Malfunction ·EV3 NEUROVASCULAR·Product code MJN·February 21, 2013

    UNKNOWN PINNACLE METAL LINER

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·July 31, 2014

    ARTELON CMC SPACER

    FDA Adverse Event
    Injury ·ARTIMPLANT AB·Product code KYI·January 18, 2011