BEUDAMED
    10 results · 23ms · 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 ×

    SCREW LOCKING

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HWC·March 14, 2012

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HWC·March 14, 2012

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES OBERDORF·Product code HWC·March 14, 2012

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HRS·March 14, 2012

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HWC·March 14, 2012

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·March 19, 2013

    MINI-CAP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·March 9, 2011

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·March 11, 2008

    11MM/130 DEG TI CANN TROCH FIXATION NAIL 360MM/LEFT

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code HSB·February 11, 2016

    3.5MM TI LCP® PROXIMAL HUMERU PLATE-STANDARD 3H SHAFT/90MM

    FDA Adverse Event
    Injury ·SYNTHES RARON·Product code KTW·February 16, 2016