BEUDAMED
    11 results · 25ms · 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

    LIBERTY CYCLER

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code FKX·March 10, 2014

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·October 24, 2007

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 31, 2012

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

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

    KINETRA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·August 7, 2014

    BLAKE DRAIN UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GBX·March 6, 2018