BEUDAMED
    5 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 ×

    1.5MM RESORB ORBITAL FLOOR PL 24MMX24MM W/BENDING TEMP-STER

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code JEY·November 2, 2012

    BOOMERANG PEEK FUSION DEVICE

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code MQP·January 14, 2011

    NUPRO PROPHY PASTE

    FDA Adverse Event
    Injury ·DENTSPLY PROFESSIONAL·Product code EJR·March 21, 2013

    TOTALCARE SPO2RT

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·March 22, 2011

    SILICONE ADVANCED OPTIC-VIOLET SHIELD

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB·Product code HQL·April 16, 2008